[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

EP1871167A2 - Synergistic fungicidal active substance combinations - Google Patents

Synergistic fungicidal active substance combinations

Info

Publication number
EP1871167A2
EP1871167A2 EP06723755A EP06723755A EP1871167A2 EP 1871167 A2 EP1871167 A2 EP 1871167A2 EP 06723755 A EP06723755 A EP 06723755A EP 06723755 A EP06723755 A EP 06723755A EP 1871167 A2 EP1871167 A2 EP 1871167A2
Authority
EP
European Patent Office
Prior art keywords
group
methyl
carboxamide
phenyl
chloro
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP06723755A
Other languages
German (de)
French (fr)
Inventor
Ulrike Wachendorff-Neumann
Peter Dahmen
Ralf Dunkel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer Intellectual Property GmbH
Original Assignee
Bayer CropScience AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of EP1871167A2 publication Critical patent/EP1871167A2/en
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
    • A01N31/16—Oxygen or sulfur directly attached to an aromatic ring system with two or more oxygen or sulfur atoms directly attached to the same aromatic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/10—Sulfones; Sulfoxides
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
    • A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
    • A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
    • A01N43/30—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/32—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
    • A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
    • A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals

Definitions

  • the present invention relates to novel Wirkstoffkorribinationen, consisting of known carboxamides on the one hand and other known fungicidal active ingredients on the other hand and are very suitable for controlling unwanted phytopathogenic fungi.
  • R is hydrogen or methyl
  • G is hydrogen, fluorine or methyl
  • R 1 is hydrogen, halogen, C 1 -C 3 -alkyl or C r C 3 -haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms,
  • A is one of the following radicals Al or A2:
  • X is CH or N
  • R 2 is methyl, difluoromethyl or trifluoromethyl
  • R 3 is hydrogen or fluorine
  • R 4 is difluoromethyl or trifluoromethyl
  • the compounds of group (1) are generally defined by the formula (I).
  • R is hydrogen or methyl
  • G is hydrogen or methyl
  • R 1 is hydrogen, fluorine, chlorine, methyl, ethyl, n-, iso-propyl, monofluoromethyl, difluoromethyl, trifluoromethyl, monochloromethyl, dichloromethyl or trichloromethyl,
  • A is one of the following radicals Al or A2:
  • X is CH or N
  • R 2 is methyl, difluoromethyl or trifluoromethyl
  • R 3 is hydrogen or fluorine
  • R is difluoromethyl or trifluoromethyl.
  • the formula (T) comprises in particular the following preferred mixing partners of group (1):
  • N- [2- (1,3-dimethylbutyl) -3-i-mylanyl] -1-methyl-3- (trifluoromethyl) -1H-pyrazole-4-carboxamide (cf. Group 1) contains one or more, preferably one, mixing partner of groups (2) to (23).
  • N- [2- (l, 3-dimethylbutyl) -3-thienyl] -1-methyl4- (trifluoromethyl) -1H-pyrrole-3-carboxamide (group 1 ) contains one or more, preferably one, mixing partner of groups (2) to (23).
  • carboxarmetal (group 1) contains one or more, preferably one, mixing partner of groups (2) to (23).
  • the compound (6-6) carpropamid has three asymmetric substituted carbon atoms.
  • the compound (6-7) may therefore be present as a mixture of different isomers or in the form of a single component.
  • Particularly preferred are the compounds (IS, 3i?) - 2,2-dichloro-N- [(1R) -1- (4-chlorophenyl) ethyl] -1-ethyl-3-methylcyclopropanecarboxamide of the formula
  • the following active substances of groups (2) to (23) are preferred as mixing partners: (2-1) fluoxastrobin, (2-2) (2 lb) -2- (2 - ⁇ [6- (3-chloro-2-one] methylphenoxy) -5-fluoro-4-pyrimidinyl] oxy ⁇ phenyl) -2- (methoxyimino) -N-methylethaneamide, (2-3) trifloxystrobin, (2-4) (2 ⁇ , -2- (metb.oxyirnino) -N-methyl-2- (2 - ⁇ [( ⁇ (1-yl) [3- (trifluorominal) -phenyl] e-halo ⁇ amino) oxy] -methyl (1-yl) -phenyl) ethanamide, (2-5 ) (2 lb) -2- (methoxy) -N-methyl-2- ⁇ 2 - [(i ⁇ - ( ⁇ amide, (2-7) 5-methoxy-2-me% l-4
  • the following active substances of groups (2) to (23) are particularly preferred as mixing partners: (2-1) fluoxastrobin, (2-2) (2 ⁇ -2- (2 - ⁇ [6 ⁇ 3-C-nor-2-methylphenoxy ) -5-fluoro-4-pyriaminidinyl] oxy ⁇ phenyl) -2- (methoxyquinone) -N-methylethanamide, (2-3) trifloxystrobin, (3-15) prothioconazole, (3-17) tebuconazole, (3 -21) bitertanol, (3-22) triadimenol, (3-24) fluquinconazole, (4-1) dichlorofluanide, (4-2) tolylfluoride, (5-1) iprovalicarb, (6-5) fenhexamide, ( 6-6) carpropamide, (6-8) picobenzamide, (7-4) propyneb, (8-3) benalaxyl-M, (9-2) pyrimethanil, (10-
  • preferred active substance combinations consist of two groups of active compounds and each contain at least one carboxamide of the formula (I) (group 1) and at least one active compound of the stated group (2) to (23). These combinations are the Wirkstoffkombinatio ⁇ en A to R.
  • strobilurin Group 2 is selected from the following list: (2-1) fluoxastrobin, (2-2) (2E) -2- (2 - ⁇ [6- (3-chloro -2-methylphenoxy) - 5-fluoro-4-pyrirnidinyl] oxy ⁇ phenyl) -2- (memoxy-imino) -N-methylethanamide, (2-3) trifloxystrobin, (2-8) dimoxystrobin, (2-9) picoxystrobin, (2-10) Pyraclostrobin.
  • Preferred combinations of active compounds B are those in which the triazole (group 3) is selected from the following list: (3-1) azaconazoles, (3-2) etaconazoles, (3-3) propiconazoles, (3-4) difenoconazoles, (3 5) bromuconazoles, (3-6) cyproconazoles, (3-7) hexaconazoles, (3-8) penconazoles, (3-9) myclobutanil, (3-10) tetraconazoles, (3-11) flutriafol, (3-12 ) Epoxiconazoles, (3-13) flusilazoles, (3-14) simeconazoles, (3-15) prothioconazoles, (3-16) fenbuconazoles, (3-17) tebuconazoles, (3-18) ipconazoles, (3-19) Metcon- azoles, (3-20) triticonazole, (3-21) bitertanol, (3-22) triadimenol, (3-23) triadime
  • triazole (group 3) is selected from the following list: (3-3) propiconazoles, (3-4) difenoconazoles, (3-6) cyproconazoles, (3-7) hexaconazoles, (3-15) prothioconazole, (3-17) tebuconazole, (3-19) metconazole, (3-21) bitertanol, (3-22) triadimenol, (3-24) fluquinconazole.
  • Preferred combinations of active compounds are C, in which the sulfenamide (group 4) is selected from the following list: (4-1) dichlorofluanide, (4-2) tolylfluanid.
  • carboxamide (group 6) is selected from the following list: (6-1) 2-chloro-N- (1,1,3-trimethyl-indan-4-yl) -nicotinamide, (6 -2) boscalid, (6-3) furametpyr, (6-4) ethaboxam, (6-5) fenhexamide, (6-6) carpropamide, (6-7) 2-chloro-4- (2-fluoro-2 -methyl-propionylamino) -N, N-dimethylbenzamide, (6-8) picobenzamide, (6-9) zoxamides, (6-10) 3,4-dichloro-N- (2-cyanophenyl) isothiazole-5-carboxamide, (6-11) carboxyne, (6-12) tiadinil, (6-13) silthiofam.
  • carboxamide (group 6) is selected from the following list: (6-2) boscalid, (6-4) ethaboxam, (6-5) fenhexamide, (6-6) carpropamide, (6-7) 2-Chloro-4- (2-fluoro-2-methylpropionylamino) -N, N-dimethylbenzamide, (6-8) picobenzamide, (6-9) zoxamide, (6- 10) 3,4-dichloro-N- (2-cyanophenyl) isothiazole-5-carboxamide.
  • carboxamide (group 6) is selected from the following list: (6-2) boscalid, (6-5) fenhexamide, (6-6) carpropamide, (6-8) picobenzamide.
  • Preferred active ingredient combinations are F, wherein the dithiocarbamate (group 7) is selected from the following list: (7-1) mancozeb, (7-2) maneb, (7-4) propineb, (7-5) thiram, (7 6) Zineb.
  • the dithiocarbamate (group 7) is selected from the following list: (7-1) mancozeb, (7-4) propineb.
  • active ingredient combinations G in which the acylalanine of the formula (VT) (group 8) is selected from the following list: (8-5) benalaxyl-M.
  • Preferred combinations of active compounds are H, wherein the anilino-pyrimidine (group 9) is selected from the following list: (9-1) cyprodine, (9-2) pyrimethanil.
  • Preferred active ingredient combinations are K, wherein the dicarboximide (group 12) is selected from the following list: (12-2) folpet, (12-3) iprodione.
  • Preferred combinations of active agents are N, wherein the morpholine (group 15) is selected from the following list: (15-1) aldimorph, (15-2) tridemorph, (15-3) dodemorph, (15-4) fenpropimorph.
  • Particularly preferred are drug combinations N, wherein the morpholine (group 15) is selected from the following list: (15-4) fenpropimorph.
  • Preferred combinations of active compounds are O, wherein the fungicide (group 19) is selected from the following list: (19-1) acibenzolar-S-methyl, (19-3) famoxadone, (19-4) oxadixyl, (19-5) spirox - amines, (19-8) fenamidone, (19-14) N - ( ⁇ 4 - [(cyclopropylamino) carbonyl] phenyl ⁇ sulfonyl) -2-methoxybenzamide, (19-15) 2- (4-chlorophenyl) -N- ⁇ 2- [3-methoxy-4- (prop-2-yn-1-yloxy) phenyl] ethyl ⁇ -2- (prop-2-yn-1-ylxy) acetamide.
  • the fungicide (group 19) is selected from the following list: (19-1) acibenzolar-S-methyl, (19-3) famoxadone, (19-4) oxadixy
  • active ingredient combinations O in which the fungicide (group 19) is selected from the following list: (19-5) spiroxamine, (19-14) N - ( ⁇ 4 - [(cyclopropylamino) carbonyl] -phenyl ⁇ sulfonyl) - 2-methoxybenzamide, (19-15) 2- (4-chlorophenyl) -N- ⁇ 2- [3-methoxy-4- (prop-2-yn-1-yloxy) phenyl] ethyl ⁇ -2- (propyl) 2-in-1-oxy) acetamide.
  • the fungicide (group 19) is selected from the following list: (19-5) spiroxamine, (19-14) N - ( ⁇ 4 - [(cyclopropylamino) carbonyl] -phenyl ⁇ sulfonyl) - 2-methoxybenzamide, (19-15) 2- (4-chlorophenyl) -N- ⁇ 2- [3-methoxy-4- (prop-2-yn
  • Preferred combinations of active compounds Q are those wherein the triazolopyrimidine (group 22) is selected from the following list: (22-1) 5-chloro-N - [(75,2,2,2-trifluoro-1-methylethyl) -6- ( 2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-2) 5-chloro- N - [(7i?> L, 2 -dimethylpropyl] -6- (2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-3) 5-chloro-6- ( 2-chloro-6-fluorophenyl) -7- (4-methylpiperidin-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine, (22-4) 5-chloro-6- (2 , 4,6-trifluorophenyl) -7- (4
  • triazolopyrimidine (group 22) is selected from the following list: (22-1) 5-chloro-N- [f 2 S> 2,2,2-trifluoro-1-methylethyl] -6- ( 2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-2) 5-chloro-N - [(7i-1, 2- dimethylpropyl] -6- (2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-4) 5-chloro-6- (2,4 , 6-trifluorophenyl) - 7- (4-methylpiperidm-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine, (22-5) 5-chloro-6- (2,4, 6-trifluorophenyl) -N- [(i5) -
  • Preferred combinations of active compounds R are those in which the iodochromone (group 23) is selected from the following list: (23-1) 2-butoxy-6-iodo-3-propyl-benzo-pyran-4-one, (23-2) 2-ethoxy-6 -iod-3-propyl-benzopyran-4-one, (23-3) 6-iodo-2-propoxy-3-propyl-benzopyran-4-one, (23-4) 2-but-2-ynyloxy-6 iodo-3-propyl-benzo-pyran-4-one, (23-5) 6-iodo-2- (1-methyl-butoxy) -3-propyl-benzopyran-4-one, (23-6) 2-But 3-enyloxy-6-iodobenzopyran-4-one, (23-7) 3-butyl-6-iodo-2-isopropoxy-benzopyran-4-one.
  • active ingredient combinations T in which the iodochromone (group 23) is selected from the following list: (23-1) 2-butoxy-6-iodo-3-propyl-benzopyran-4-one, (23-2) 2- Ethoxy-6-iodo-3-propyl-benzopyran-4-one.
  • the active compound combinations according to the invention contain, in addition to an active compound of the formula (I), at least one active compound of the compounds of groups (2) to (23). You may also contain other fungicidal Zumischkomponenten. If the active ingredients in the active compound combinations according to the invention are present in certain weight ratios, the synergistic effect is particularly pronounced. However, the weight ratios of the active ingredients in the drug combinations can be varied within a relatively wide range. In general, combinations of active compounds according to the invention of the formula (J) and a mixing partner from one of the groups (2) to (23) mix ratios exemplified in the following in the table. "19
  • the mixing ratios are based on weight ratios.
  • the ratio is to be understood as active substance of the formula (T): Mischpartner.
  • the mixing ratio should be such that a synergistic mixture is obtained.
  • the mixing ratios between the compound of formula (I) and a compound of any of groups (2) to (23) may also vary between the individual compounds of a group.
  • the active compound combinations according to the invention have very good fungicidal properties and can be used for controlling phytopathogenic fungi and bacteria.
  • Fungicides can be used for the control of Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes.
  • Bactericides can be used in crop protection for controlling Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
  • Blumeria species such as Blumeria graminis
  • Podosphaera species such as Podosphaera leucotricha
  • Sphaerotheca species such as Sphaerotheca fuliginea
  • Uncinula species such as Uncinula necator
  • Gymnosporangium species such as, for example, Gymnosporangium sabinae
  • Hemileia species such as, for example, Hemileia vastatrix
  • Phakopsora species such as Phakopsora pachyrhizi and Phakopsora meibomiae
  • Puccinia species such as Puccinia recondita
  • Uromyces species such as Uromyces appendiculatus
  • Bremia species such as Bremia lactucae
  • Peronospora species such as Peronospora pisi or P. brassicae;
  • Phytophthora species such as Phytophthora infestans
  • Plasmopara species such as Plasmopara viticola
  • Pseudoperonospora species such as, for example, Pseudoperonospora humuli or Pseudoperonospora cubensis;
  • Pythium species such as Pythium ultimum; Leaf spot diseases and leaf withering, caused by eg
  • Alternaria species such as Alternaria solani;
  • Cercospora species such as Cercospora beticola
  • Cladiosporum species such as Cladiosporium cucumerinum
  • Cochliobolus species such as Cochliobolus sativus
  • Drechslera (Conidic form: Drechslera, Syn: Helminthosporium);
  • Colletotrichum species such as Colletotrichum lindemuthanium
  • Cycloconium species such as cycloconium oleaginum
  • Diaporthe species such as Diaporthe citri
  • Elsinoe species such as Elsinoe fawcettii
  • Gloeosporium species such as, for example, Gloeosporium laeticolor
  • Glomerella species such as Glomerella cingulata
  • Guignardia species such as Guignardia bidwelli;
  • Leptosphaeria species such as Leptosphaeria maculans
  • Magnaporthe species such as Magnaporthe grisea
  • Mycosphaerella species such as Mycosphaerelle graminicola
  • Phaeosphaeria species such as Phaeosphaeria nodorum
  • Pyrenophora species such as, for example, Pyrenophora teres
  • Ramularia species such as Ramularia collo-cygni
  • Rhynchosporium species such as Rhynchosporium secalis
  • Septoria species such as Septoria apii
  • Typhula species such as Typhula incarnata
  • Venturia species such as Venturia inaequalis
  • Corticium species such as Corticium graminearum
  • Fusarium species such as Fusarium oxysporum
  • Gaeumannomyces species such as Gaeumannomyces graminis
  • Rhizoctonia species such as Rhizoctonia solani
  • Tapesia species such as Tapesia acuforrnis
  • Thielaviopsis species such as Thielaviopsis basicola
  • Ear and panicle diseases caused by e.g. Alternaria species, such as Alternaria spp .; Aspergillus species, such as Aspergillus flavus;
  • Cladosporium species such as Cladosporium spp .; Claviceps species, such as Claviceps purpurea; Fusarium species such as Fusarium culmorum; Gibberella species, such as Gibberella zeae; Monographella species, such as Monographella nivalis;
  • Sphacelotheca species such as Sphacelotheca reiliana
  • Tilletia species such as Tilletia caries
  • Urocystis species such as Urocystis occulta
  • Ustilago species such as Ustilago nuda
  • Phytophthora species such as Phytophthora cactorum
  • Pythium species such as Pythium ultimum
  • Rhizoctonia species such as Rhizoctonia solani
  • Sclerotium species such as Sclerotium rolfsii
  • Nectria species such as Nectria galligena
  • Wilting diseases caused by eg Monilinia species such as Monilinia laxa;
  • Degenerative diseases of woody plants caused by eg Esca species, such as Phaemoniella clamydospora; Floral and seed diseases caused by, for example, Botrytis species such as Botrytis cinerea;
  • Rhizoctonia species such as Rhizoctonia solani
  • Xanthomonas species such as Xanthomonas campestris pv. Oryzae
  • Pseudomonas species such as Pseudomonas syringae pv. Lachiymans
  • Erwinia species such as Erwinia amylovora
  • the following diseases of soybean beans can be controlled:
  • Anthracnose (Colletotrichum gloeosporoides dematium var. Truncatum), Brown spot (Septoria glycines), Cercospora leaf spot and blight (Cercospora mkuchii), Choanephora leaf blight (Choanephora infundibulifera trispora (Syn.)), Alternaria leaf spot (Alternaria spec.
  • Dactuliophora leaf spot (Dactuliophora glycines), Downy Mildew (Peronospora manshurica), Drechslera blight (Drechslera glycini), Frogeye leaf spot (Cercospora sojina), Leptosphaerulina leaf spot (Leptosphaerulina trifolii), Phyllostica leaf spot (Phyllosticta sojaecola), Powdery Mildew (Phyllosticta sojaecola) Microsphaera diffusa), Pyrenochaeta Leaf Spot (Pyrenochaeta glycines), Rhizoctonia Aerial, Foliage and Web Blight (Rhizoctonia solani), Rust (Phakopsora pachyrhizi), Scab (Sphaceloma glycines), Stemphylium Leaf Blight (Stemphylium botryosum), Target
  • Phytophthora red (Phytophthora megasperma), Brown Stem Red (Phialophora gregata), Pythium Red (Pythium aphanidermatum, Pythium irregular , Pythium debaryanum, Pythium myriotylum, Pythium ultimum), Rhizoctonia Root Red, Stem Decay, and Damping Off (Rhizoctonia solani), Sclerotinia Stem Decay (Sclerotinia sclerotiorum), Sclerotinia Southern Blight (Sclerotinia rolfsii), Thielaviopsis Root Red (Thielaviopsis basicola) ,
  • the good plant tolerance of the active substance combinations in the concentrations necessary for the control of plant diseases makes it possible to treat whole plants (upper plants). plant parts and roots), of plant and seed, and of the soil.
  • the active substance combinations according to the invention can be used for blush application or else as mordant.
  • the good plant tolerance of the usable active ingredients in the concentrations necessary for the control of plant diseases allows a treatment of the seed.
  • the active compounds according to the invention can thus be used as mordants.
  • methods for treating seed should also include the intrinsic fungicidal properties of transgenic plants in order to achieve optimum protection of the seed and the germinating plant with a minimum of pesticide use.
  • the present invention therefore more particularly relates to a method of protecting seeds and germinating plants from the infestation of phytopathogenic fungi by treating the seed with an agent according to the invention.
  • the invention also relates to the use of the seed treatment agents of the invention for protecting the seed and the germinating plant from phytopathogenic fungi.
  • the invention relates to seed which has been treated with an agent according to the invention for protection against phytopathogenic fungi.
  • One of the advantages of the present invention is that because of the particular systemic properties of the compositions of the invention, treatment of the seed with these agents not only protects the seed itself but also the resulting plants after emergence from phytopathogenic fungi. In this way, the immediate treatment of the culture at the time of sowing or shortly afterwards can be omitted.
  • mixtures according to the invention can also be used in particular in the case of transgenic seed.
  • compositions according to the invention are suitable for the protection of seeds of any plant variety used in agriculture, in the greenhouse, in forests or in horticulture.
  • these are seeds of cereals (such as wheat, barley, rye, millet and oats), corn, cotton, soy, rice, potatoes, sunflower, bean, coffee, turnip (eg sugarbeet and fodder), peanut, vegetables ( like tomato, cucumber, onions and lettuce), lawn and ornamental plants.
  • cereals such as wheat, barley, rye, millet and oats
  • turnip eg sugarbeet and fodder
  • peanut like tomato, cucumber, onions and lettuce
  • the agent according to the invention is applied to the seed alone or in a suitable formulation.
  • the seed is treated in a condition that is so stable that no damage occurs during the treatment.
  • the treatment of the seed can be done at any time between harvesting and sowing.
  • seed is used which has been separated from the plant and freed from flasks, shells, stems, hull, wool or pulp.
  • seed may be used which has been harvested, cleaned and dried to a moisture content below 15% by weight.
  • seed can also be used, which after drying, for example, treated with water and then dried again.
  • the agents according to the invention can be applied directly, ie without containing further components and without being diluted.
  • suitable formulations and methods for seed treatment are known to those skilled in the art and are described e.g. in the following documents: US 4,272,417 A, US 4,245,432 A, US 4,808,430 A, US 5,876,739 A, US 2003/0176428 A1, WO 2002/080675 A1, WO 2002/028186 A2.
  • the active compound combinations according to the invention are also suitable for increasing crop yield. They are also low toxicity and have good plant tolerance.
  • plants and parts of plants can be treated.
  • plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
  • Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant variety rights.
  • Plant parts are to be understood as meaning all aboveground and subterranean parts and organs of the plants, such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes.
  • the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
  • the treatment according to the invention of the plants and plant parts with the active ingredients is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, spreading, spreading and in propagation material, in particular in seeds, further by single or multi-layer wrapping.
  • all plants and their parts can be treated.
  • wild or conventional biologic treated genetic breeding methods such as hybridization or protoplast fusion obtained plant species and plant varieties and their parts.
  • transgenic plants and plant cultivars obtained by genetic engineering if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
  • the term “parts” or “parts of plants” or “plant parts” has been explained above.
  • the treatment according to the invention may also give rise to superadditive ("synergistic") effects, for example reduced application rates and / or extensions of the activity spectrum and / or a Enhancement of the effect of the substances and agents usable according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to water or soil salt content, increased flowering efficiency, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or workability of the harvested products possible, which go beyond the actual expected effects.
  • superadditive for example reduced application rates and / or extensions of the activity spectrum and / or a Enhancement of the effect of the substances and agents usable according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to water or soil salt content, increased flowering efficiency, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or
  • the preferred plants or plant cultivars to be treated according to the invention include all plants which have obtained genetic material by the genetic modification which gives these plants particularly advantageous valuable properties ("traits”.) Examples of such properties are better Plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or soil salt content, increased flowering efficiency, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or Further and particularly emphasized examples of such properties are an increased defense of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and / or Vir and increased tolerance of the plants to certain herbicidal active substances.
  • transgenic plants include the important crops such as cereals (wheat, rice), corn, soy, potato, cotton, rapeseed and fruit plants (with the fruits apples, pears, citrus fruits and grapes), with corn, soy, potato, cotton and rapeseed should be highlighted.
  • Traits are particularly raised the increased defense of the plants against insects by toxins formed in the plants, in particular those by the genetic material from Bacillus thuringiensis (eg by the genes Cry ⁇ A (a), CryIA (b), CryIA (c), CryJIA, CrylllA, CrylHB2, Cry9c Cry2Ab, Cry3Bb and CrylF and their combinations) in the plants (hereinafter "Bt plants”) .
  • Bt plants The traits which are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones.
  • Sulfonylureas, glyphosate or phosphinotricin eg "PAT" gene
  • the genes which confer the desired properties can also be present in combinations with one another in the transgenic plants.
  • “Bt plants” are maize varieties, cotton varieties, soya bean varieties and potato varieties may be mentioned that under the trade names yeeld GARD ® (for example maize, cotton, soya beans), KnockOut ® (for example maize), StarLink ® (for example maize), Bollgard ® ( cotton), Nucotn® (cotton) and NewLeaf ® (potato).
  • herbicide-tolerant plants are maize varieties, cotton varieties and soybean varieties may be mentioned that, under the trade names Roundup Ready ® (tolerance to glyphosate, for example maize, cotton, soybeans) Liberty Link® (tolerance to phosphinotricin, eg rapeseed), IMI® (tolerance to imidazolmone) and STS® (tolerance to sulfonylureas eg maize) are also marketed as herbicide-resistant (conventionally grown on herbicide tolerance) plants Clearf ⁇ eld ® mentioned varieties (eg maize) Of course, these statements also apply to future developed or future on the market Pfl cultivars with these or future developed genetic traits.
  • Roundup Ready ® tolerance to glyphosate, for example maize, cotton, soybeans
  • Liberty Link® tolerance to phosphinotricin, eg rapeseed
  • IMI® to imidazolmone
  • STS® tolerance to sulf
  • the active compound combinations according to the invention can be converted into the customary formulations depending on their respective physical and / or chemical properties, such as solutions, emulsions, suspensions, powders, dusts, foams, pastes, soluble powders, granules, aerosols, suspension-emulsion concentrates, Active substance-impregnated natural and synthetic substances as well as ultra-fine encapsulations in polymeric substances and in coating compositions for seeds, as well as ULV-KaIt and warm mist formulations.
  • formulations are prepared in a known manner, e.g. by mixing the active compounds or the active compound combinations with extenders, ie liquid solvents, liquefied gases under pressure and / or solid carriers, optionally with the use of surface-active agents, ie emulsifiers and / or dispersants and / or foam-forming agents.
  • extenders ie liquid solvents, liquefied gases under pressure and / or solid carriers
  • surface-active agents ie emulsifiers and / or dispersants and / or foam-forming agents.
  • organic solvents can also be used as auxiliary solvents.
  • liquid solvents are essentially in question: Aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols, such as butanol or glycol, and their ethers and esters , Ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
  • liquefied gaseous diluents or carriers are meant those liquids which are gaseous at normal temperature and under normal pressure, e.g. Aerosol propellants, such as butane, propane, nitrogen and carbon dioxide.
  • Suitable solid carriers are: e.g. Ammonium salts and ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as fumed silica, alumina and silicates.
  • Suitable solid carriers for granules are: e.g. Cracked and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, coconut shells, corn cobs and tobacco stems.
  • Suitable emulsifying and / or foaming agents are: e.g.
  • nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolysates.
  • Suitable dispersants are: e.g. Lignin sulphite waste liquors and methyl cellulose.
  • adhesives such as carboxymethyl cellulose, natural and synthetic see powdery, granular or latex-like polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins, and synthetic phospholipids.
  • Other additives may be mineral and vegetable oils.
  • Dyes such as inorganic pigments such as iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used.
  • the active substance content of the application forms prepared from the commercial formulations can vary within wide ranges.
  • the active ingredient concentration of the use forms for controlling animal pests such as insects and acarids may be from 0.0000001 to 95% by weight of active compound, preferably between 0.0001 and 1% by weight.
  • the application is done in a custom forms adapted to the application forms.
  • the formulations for controlling undesired phytopathogenic fungi generally contain between 0.1 and 95% by weight of active ingredients, preferably between 0.5 and 90%.
  • the active compound combinations according to the invention can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, emulsifiable concentrates, emulsions, suspensions, wettable powders, soluble powders, dusts and granules.
  • the application is done in the usual way, e.g. by pouring (drenchen), drip irrigation, spraying, spraying, scattering, dusting, foaming, brushing, spreading, dry pickling, wet pickling, wet pickling, slurry pickling, encrusting, etc.
  • the active compound combinations according to the invention can be present in commercially available formulations as well as in the formulations prepared from these formulations in admixture with other active ingredients, such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances or herbicides.
  • active ingredients such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances or herbicides.
  • the application rates can be varied within a substantial range, depending on the mode of administration.
  • the application rates of active compound combination are generally between 0.1 and 10,000 g / ha, preferably between 10 and 1,000 g / ha.
  • the application rates of active ingredient combination are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 10 g per kilogram of seed.
  • the application rates of active ingredient combination are generally between 0.1 and 10,000 g / ha, preferably between 1 and 5,000 g / ha.
  • the active compound combinations can be used as such, in the form of concentrates or generally customary formulations such as powders, granules, solutions, suspensions, emulsions or pastes.
  • the formulations mentioned can be prepared in a manner known per se, for example by mixing the active compounds with at least one solvent or diluent, emulsifier, dispersing and / or binding or fixing agent, water repellent, optionally siccatives and UV stabilizers and optionally Dyes and pigments and other processing aids.
  • the good fungicidal action of the active compound combinations according to the invention is evident from the examples below. While the individual active ingredients have weaknesses in the fungicidal action, the combinations show an effect that goes beyond a simple effect of turning.
  • a synergistic effect is always present in fungicides when the fungicidal action of the drug combinations is greater than the sum of the effects of the individually applied active ingredients.
  • X means the efficiency when using the active ingredient A in an application rate of m ppm
  • Y means the efficiency when using the active ingredient B in an application rate of n ppm
  • E means the efficiency when using the active compounds A and B in application rates of m and n ppm
  • the efficiency is determined in%. It means 0% an efficiency that corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
  • the combination is over-additive in its effect, ie there is a synergistic effect.
  • the actual observed efficiency must be greater than the expected efficiency value (E) calculated from the above formula.
  • Emulsifier 1 weight of alkylaryl polyglycol ether
  • the plants are then placed in a greenhouse at a temperature of about 20 0 C and a relative humidity of 80% to promote the development of rust pustules.
  • ** calc. calculated according to the Colby formula - -
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • the plants are spotted with spores of Erysiphe graminis f.sp. tritici pollinated.
  • the plants are grown in a greenhouse at a temperature of about 20 0 C and a relative
  • Humidity of about 80% set up to favor the development of powdery mildew pustules.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The novel active substance combinations are produced from a carboxamide of general formula (I) (group 1), wherein R, G, R1 and A are defined as in the description, and active substance groups (2) to (23) listed in the description and have excellent fungicidal properties.

Description

Synergistische fungizide WirkstoffkombinationenSynergistic fungicidal drug combinations
Die vorliegende Erfindung betrifft neue Wirkstoffkorribinationen, die aus bekannten Carboxamiden einerseits und weiteren bekannten fungiziden Wirkstoffen andererseits bestehen und sehr gut zur Bekämpfung von unerwünschten phytopathogenen Pilzen geeignet sind.The present invention relates to novel Wirkstoffkorribinationen, consisting of known carboxamides on the one hand and other known fungicidal active ingredients on the other hand and are very suitable for controlling unwanted phytopathogenic fungi.
Es ist bereits bekannt, dass bestimmte Carboxamide fungizide Eigenschaften besitzen: z.B. N-[2-(l,3- Dimethylbutyl)-3-1hienyl]-l-methyl-3-(trifluormethyl)-lH-pyrazol-4-carboxarnid aus EP-A 0 737682. Die Wirksamkeit dieser Stoffe ist gut, lässt aber bei niedrigen Aufwandmengen in manchen Fällen zu wünschen übrig. Ferner ist schon bekannt, dass zahlreiche Triazol-Derivate, Anilin-Derivate, Dicarb- oximide und andere Heterocyclen zur Bekämpfung von Pilzen eingesetzt werden können (vgl. EP-A 0040345, DE-A 2201 063, DE-A 23 24010, Pestizide Manual, 9th. Edition (1991), Seiten 249 und 827, EP-A 0 382 375 und EP-A 0 515 901). Auch die Wirkung dieser Stoffe ist aber bei niedrigen Aufwandmengen nicht immer ausreichend. Ferner ist bereits bekannt, dass l-(3,5-Dimethyl-isoxazol-4- sulfonyl)-2-chlor-6,6-difluor-[l,3]-dioxolo-[4,5fJ-benzimidazol fungizide Eigenschaften besitzt (vgl. WO 97/06171). Schließlich ist auch bekannt, dass substituierte Halogenpyrimidine fungizide Eigenschaften besitzen (vgl. DE-Al-19646407, EP-B-712 396).It is already known that certain carboxamides have fungicidal properties: e.g. N- [2- (l, 3-dimethylbutyl) -3-1hienyl] -1-methyl-3- (trifluoromethyl) -1H-pyrazole-4-carboxamide from EP-A 0 737 682. The effectiveness of these substances is good but at low rates in some cases to be desired. Furthermore, it is already known that numerous triazole derivatives, aniline derivatives, dicarboximides and other heterocycles can be used for combating fungi (compare EP-A 0040345, DE-A 2201 063, DE-A 23 24010, Pesticides Manual , 9th edition (1991), pages 249 and 827, EP-A 0 382 375 and EP-A 0 515 901). However, the effect of these substances is not always sufficient at low application rates. Furthermore, it is already known that l- (3,5-dimethylisoxazole-4-sulfonyl) -2-chloro-6,6-difluoro [1,3] -dioxolo- [4,5fJ-benzimidazole possesses fungicidal properties ( see WO 97/06171). Finally, it is also known that substituted halopyrimidines have fungicidal properties (cf., DE-Al-19646407, EP-B-712 396).
Auch diverse Mischungen von Alkylthienylcarboxamiden sind bekannt. Auch diese lassen in manchen Fällen in ihrer Wirkung zu wünschen übrig (vgl. JP-A 11-292715, JP-A 11-302107, JP-A 11-302108, JP-A 11-302109, JP-A 11-302110, JP-A 11-302111, JP-A 2001-72511, JP-A 2001-72512, JP-A 2001- 72513, JP-A 11-322513, JP-A 11-322514, JP-A 2000-53506 und JP-A 2000-53507).Various mixtures of Alkylthienylcarboxamiden are known. These, too, in some cases leave something to be desired in their effect (see JP-A 11-292715, JP-A 11-302107, JP-A 11-302108, JP-A 11-302109, JP-A 11-302110, JP-A 11-302111, JP-A 2001-72511, JP-A 2001-72512, JP-A 2001-72513, JP-A 11-322513, JP-A 11-322514, JP-A 2000-53506 and JP -A 2000-53507).
Es wurden nun neue Wirkstoffkombinationen mit sehr guten fungiziden Eigenschaften gefunden, enthaltend ein Carboxamid der allgemeinen Formel (!) (Gruppe 1)New active compound combinations with very good fungicidal properties have now been found, containing a carboxamide of the general formula (I) (group 1)
(T), in welcher(T), in which
R für Wasserstoff oder Methyl steht,R is hydrogen or methyl,
G für Wasserstoff, Fluor oder Methyl steht,G is hydrogen, fluorine or methyl,
R1 für Wasserstoff, Halogen, C1-C3-AIkVl oder CrC3-Halogenalkyl mit 1 bis 7 Fluor-, Chlor- und/oder Bromatomen steht,R 1 is hydrogen, halogen, C 1 -C 3 -alkyl or C r C 3 -haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms,
A für einen der folgenden Reste Al oder A2 steht: A is one of the following radicals Al or A2:
X für CH oder N steht,X is CH or N,
R2 für Methyl, Difluormethyl oder Trifluormethyl steht,R 2 is methyl, difluoromethyl or trifluoromethyl,
R3 für Wasserstoff oder Fluor steht,R 3 is hydrogen or fluorine,
R4 für Difluormethyl oder Trifluormethyl steht,R 4 is difluoromethyl or trifluoromethyl,
und mindestens einen Wirkstoff, der aus den folgenden Gruppen (2) bis (23) ausgewählt ist:and at least one active ingredient selected from the following groups (2) to (23):
Gruppe (2) Strobilurine (2-1) Fluoxastrobin (bekannt aus DE-A 196 02 095) der FormelGroup (2) Strobilurins (2-1) Fluoxastrobin (known from DE-A 196 02 095) of the formula
(2-2) (2-^-2-(2-{[6-(3-CMor-2-methylphenoxy)-5-fluor-4-pyrimidinyl]oxy}ρhenyl)-2-(methoxy- imino)-N-methylethanamid (bekannt aus DE-A 19646407, EP-B 0 712 396) der Formel(2-2) (2 - ^ - 2- (2 - {[6- (3-CMor-2-methylphenoxy) -5-fluoro-4-pyrimidinyl] oxy} phenyl) -2- (methoxy-imino) - N-methylethanamide (known from DE-A 19646407, EP-B 0 712 396) of the formula
(2-3) Trifloxystrobin (bekannt aus EP-A 0460 575) der Formel (2-3) Trifloxystrobin (known from EP-A 0460 575) of the formula
(2-4) (2^-2-(Memoxyimmo)-N-me%l-2-(2-{[({(l^-l-[3-(1xifluormethyl)phenyl]ethyliden}- amino)oxy]methyl}phenyl)ethanamid (bekannt aus EP-A 0 569 384) der Formel(2-4) (2 ^ -2- (Memoxy-moiety) -N-Me)% 2- (2 - {[({(1- (1-) - 1- (3- (1-fluoromethyl) -phenyl] -ethylidene-amino) -oxy ] methyl} phenyl) ethanamide (known from EP-A 0 569 384) of the formula
(2-5) (2^-2-(Methoxyimino)-N-methyl-242-[(^-({l-[3-(trifluorme%l)pheaiyl]e&oxy}imino)- methyl]phenyl}ethanamid (bekannt aus EP-A 0 596254) der Formel (2-5) (2 ^ -2- (methoxyimino) -N-methyl-242 - [(^ - ({1- [3- (trifluoromethyl) -propyl] e & oxy} imino) -methyl] -phenyl} -ethaneamide ( known from EP-A 0 596254) of the formula
(2-6) Orysastrobin (bekannt aus DE-A 195 39 324) der Formel(2-6) Orysastrobin (known from DE-A 195 39 324) of the formula
(2-7) 5-Methoxy-2-methyl-4-(2-{[({(l^)-l-[3-(trifluormethyl)phenyl]ethyliden}arnino)oxy]- methyl}phenyl)-2,4-dihydro-3H-l,2,4-triazol-3-on (bekannt aus WO 98/23155) der Formel(2-7) 5-Methoxy-2-methyl-4- (2 - {[({(l) -l- [3- (trifluoromethyl) phenyl] ethylidene} arnino) oxy] methyl} phenyl) -2 , 4-dihydro-3H-l, 2,4-triazol-3-one (known from WO 98/23155) of the formula
(2-8) Dimoxystrobin (bekannt aus EP-A 0 398 692) der Formel(2-8) Dimoxystrobin (known from EP-A 0 398 692) of the formula
(2-9) Picoxystrobin (bekannt aus EP-A 0278 595) der Formel(2-9) Picoxystrobin (known from EP-A 0278 595) of the formula
(2-10) Pyraclostrobin (bekannt aus DE-A 4423 612) der Formel(2-10) Pyraclostrobin (known from DE-A 4423 612) of the formula
- A - - A -
Gruppe (3) TriazoleGroup (3) triazoles
(3-1) Azaconazole (bekannt aus DE-A 25 51 560) der Formel(3-1) Azaconazole (known from DE-A 25 51 560) of the formula
(3-2) Etaconazole (bekannt aus DE-A 25 51 560) der Formel (3-2) Etaconazole (known from DE-A 25 51 560) of the formula
(3-3) Propiconazole (bekannt aus DE-A 25 51 560) der Formel(3-3) Propiconazole (known from DE-A 25 51 560) of the formula
(3-4) Difenoconazole (bekannt aus EP-A 0 112 284) der Formel(3-4) Difenoconazole (known from EP-A 0 112 284) of the formula
(3 -5) Bromuconazole (bekannt aus EP-A 0258 161) der Formel(3 -5) Bromuconazoles (known from EP-A 0258 161) of the formula
(3-6) Cyproconazole (bekannt aus DE-A 3406993) der Formel(3-6) Cyproconazole (known from DE-A 3406993) of the formula
(3-7) Hexaconazole (bekannt aus DE-A 3042 303) der Formel (3-7) Hexaconazole (known from DE-A 3042 303) of the formula
(3-8) Penconazole (bekannt aus DE-A 27 35 872 ) der Formel(3-8) Penconazole (known from DE-A 27 35 872) of the formula
(3-9) Myclobutanil (bekannt aus EP-A 0 145 294) der Formel(3-9) Myclobutanil (known from EP-A 0 145 294) of the formula
(3-10) Tetraconazole (bekannt aus EP-A 0 234242) der Formel(3-10) Tetraconazole (known from EP-A 0 234 242) of the formula
(3-11) Flutriafol (bekannt aus EP-A 0015 756) der Formel(3-11) Flutriafol (known from EP-A 0015 756) of the formula
(3-12) Epoxiconazole (bekannt aus EP-A 0 196038) der Formel(3-12) Epoxiconazoles (known from EP-A 0 196038) of the formula
(3-13) Flusilazole (bekannt aus EP-A 0 068 813) der Formel (3-13) Flusilazoles (known from EP-A 0 068 813) of the formula
(3-14) Simeconazole (bekannt aus EP-A 0 537 957) der Formel(3-14) Simeconazole (known from EP-A 0 537 957) of the formula
(3-15) Prothioconazole (bekannt aus WO 96/16048) der Formel (3-15) Prothioconazole (known from WO 96/16048) of the formula
(3-16) Fenbuconazole (bekannt aus DE-A 3721 786) der Formel(3-16) Fenbuconazole (known from DE-A 3721 786) of the formula
(3-17) Tebuconazole (bekannt aus EP-A 0 040345) der Formel(3-17) Tebuconazole (known from EP-A 0 040345) of the formula
(3-18) Ipconazole (bekannt aus EP-A 0 329 397) der Formel(3-18) Ipconazole (known from EP-A 0 329 397) of the formula
(3-19) Metconazole (bekannt aus EP-A 0 329 397) der Formel (3-19) Metconazole (known from EP-A 0 329 397) of the formula
(3-20) Triticonazole (bekannt aus EP-A 0 378 953) der Formel(3-20) Triticonazole (known from EP-A 0 378 953) of the formula
(3-21) Bitertanol (bekannt aus DE-A 23 24 010) der Formel(3-21) Bitertanol (known from DE-A 23 24 010) of the formula
(3-22) Triadimenol (bekannt aus DE-A 23 24010) der Formel(3-22) Triadimenol (known from DE-A 23 24010) of the formula
(3-23) Triadirαefon (bekannt aus DE-A 2201 063) der Formel(3-23) Triadirαphone (known from DE-A 2201 063) of the formula
(3-24) Fluquinconazole (bekannt aus EP-A 0 183 458) der Formel (3-24) Fluquinconazole (known from EP-A 0 183 458) of the formula
(3-25) Quinconazole (bekannt aus EP-A 0 183 458) der Formel(3-25) Quinconazole (known from EP-A 0 183 458) of the formula
Gruppe (4) Sulfenamide Group (4) sulfenamides
(4-1) Dichlofluanid (bekannt aus DE-A 11 93 498) der Formel(4-1) Dichlofluanid (known from DE-A 11 93 498) of the formula
(4-2) Tolylfluanid (bekannt aus DE-A 11 93 498) der Formel(4-2) Tolylfluanid (known from DE-A 11 93 498) of the formula
Gruppe (5) ValinamideGroup (5) Valinamide
(5-1) Iprovalicarb (bekannt aus DE-A 40 26 966) der Formel(5-1) Iprovalicarb (known from DE-A 40 26 966) of the formula
(5-2) Benthiavalicarb (bekannt aus WO 96/04252) der Formel (5-2) Benthiavalicarb (known from WO 96/04252) of the formula
Gruppe (6) CarboxamideGroup (6) carboxamides
(6-1) 2-Chloro-N-(l , 1 ,3-trimethyl-indan-4-yl)-nicotinamid (bekannt aus EP-A 0256503) der Formel(6-1) 2-chloro-N- (1,1,3-trimethyl-indan-4-yl) nicotinamide (known from EP-A 0256503) of the formula
(6-2) Boscalid (bekannt aus DE-A 195 31 813) der Formel(6-2) boscalid (known from DE-A 195 31 813) of the formula
(6-3) Furametpyr (bekannt aus EP-A 0315 502) der Formel (6-3) Furametpyr (known from EP-A 0315 502) of the formula
(6-4) Ethaboxam (bekannt aus EP-A 0639 574) der Formel(6-4) Ethaboxam (known from EP-A 0639 574) of the formula
(6-5) Fenhexamid (bekannt aus EP-A 0339418) der Formel (6-5) Fenhexamide (known from EP-A 0339418) of the formula
(6-6) Carpropamid (bekannt aus EP-A 0 341 475) der Formel(6-6) Carpropamide (known from EP-A 0 341 475) of the formula
(6-7) 2-Chlor^-(2-fluor-2-methyl-propionylamino)-N,N-dimethyl-benzamid (bekannt aus EP-A 0 600 629) der Formel(6-7) 2-Chloro - (2-fluoro-2-methylpropionylamino) -N, N-dimethylbenzamide (known from EP-A 0 600 629) of the formula
(6-8) Picobenzamid (bekannt aus WO 99/42447) der Formel(6-8) Picobenzamide (known from WO 99/42447) of the formula
(6-9) Zoxamide (bekannt aus EP-A 0 604 019) der Formel(6-9) Zoxamide (known from EP-A 0 604 019) of the formula
(6-10) 3,4-Dichlor-N-(2-cyanophenyl)isothiazol-5-carboxamid (bekannt aus WO 99/24413) der Formel (6-10) 3,4-Dichloro-N- (2-cyanophenyl) isothiazole-5-carboxamide (known from WO 99/24413) of the formula
(6-11) Carboxin (bekannt aus US 3,249,499) der Formel(6-11) Carboxin (known from US 3,249,499) of the formula
(6-12) Tiadinil (bekannt aus US 6,616,054) der Formel(6-12) Tiadinil (known from US 6,616,054) of the formula
(6-13) Silthiofam (bekannt aus WO 96/18631) der Formel(6-13) Silthiofam (known from WO 96/18631) of the formula
Gruppe (7) Dithiocarbamate Group (7) dithiocarbamates
(7-1) Mancozeb (bekannt aus DE-A 12 34 704) mit dem IUPAC-Namen(7-1) Mancozeb (known from DE-A 12 34 704) with the IUPAC name
Manganese ethylenebis(dithiocarbamate) (polymeric) complex with zinc salt (7-2) Maneb (bekannt aus US 2,504,404) der FormelManganese ethylenebis (dithiocarbamate) (polymeric) complex with zinc salt (7-2) maneb (known from US 2,504,404) of the formula
(7-3) Metiram (bekannt aus DE-A 1076434) mit dem IUPAC-Namen(7-3) Metiram (known from DE-A 1076434) with the IUPAC name
Zinc ammoniate ethylenebis(dithiocarbamate) — poly(ethylenethiuram disulfide) (7-4) Propineb (bekannt aus GB 935 981) der FormelZinc ammoniate ethylenebis (dithiocarbamate) - poly (ethylenethiuram disulfide) (7-4) Propineb (known from GB 935,981) of the formula
_Jn (7-5) Thiram (bekannt aus US 1,972,961) der Formel_Jn (7-5) Thiram (known from US 1,972,961) of the formula
(7-6) Zineb (bekannt aus DE-A 10 81 446) der Formel(7-6) Zineb (known from DE-A 10 81 446) of the formula
(7-7) Ziram (bekannt aus US 2,588,428) der Formel(7-7) Ziram (known from US 2,588,428) of the formula
Gruppe (8) AcylalanineGroup (8) acylalanines
(8-1) Benalaxyl (bekannt aus DE-A 29 03 612) der Formel(8-1) Benalaxyl (known from DE-A 29 03 612) of the formula
(8-2) Furalaxyl (bekannt aus DE-A 25 13 732) der Formel(8-2) Furalaxyl (known from DE-A 25 13 732) of the formula
(8-3) Benalaxyl-M der Formel(8-3) Benalaxyl-M of the formula
Gruppe (9): Anilino-pyrimidineGroup (9): anilino-pyrimidines
(9-1) Cyprodinil (bekannt aus EP-A 0 310 550) der Formel (9-1) Cyprodinil (known from EP-A 0 310 550) of the formula
(9-2) Pyrimethanil (bekannt aus DD 151 404) der Formel(9-2) Pyrimethanil (known from DD 151 404) of the formula
Gruppe ("IQ): BenzimidazoleGroup ( " IQ): Benzimidazoles
(10-1) 6-Chlor-5-[(3,5-dimethylisoxazol-4-yl)sulfonyl]-2,2-difluor-5H-[l,3]dioxolo[4,5-fl- benzimidazol (bekannt aus WO 97/06171) der Formel(10-1) 6-Chloro-5 - [(3,5-dimethylisoxazol-4-yl) sulfonyl] -2,2-difluoro-5H- [1,3] dioxolo [4,5-fl-benzimidazole (known from WO 97/06171) of the formula
(10-2) Benomyl (bekannt aus US 3,631,176) der Formel(10-2) Benomyl (known from US 3,631,176) of the formula
(10-3) Carbendazim (bekannt aus US 3,010,968) der Formel(10-3) Carbendazim (known from US 3,010,968) of the formula
(10-4) Chlorfenazole der Formel(10-4) Chlorfenazoles of the formula
(10-5) Fuberidazole (bekannt aus DE-A 1209 799) der Formel (10-5) Fuberidazole (known from DE-A 1209 799) of the formula
(10-6) Thiabendazole (bekannt aus US 3,206,468) der Formel (10-6) thiabendazoles (known from US 3,206,468) of the formula
Gruppe (11): Carbamate (11-1) Propamocarb (bekannt aus US 3,513,241) der FormelGroup (11): Carbamate (11-1) Propamocarb (known from US 3,513,241) of the formula
(11-2) Propamocarb-hydrochloride (bekannt aus US 3,513,241) der Formel(11-2) Propamocarb hydrochloride (known from US 3,513,241) of the formula
(11-3) Propamocarb-Fosetyl der Formel(11-3) Propamocarb-Fosetyl of the formula
Gruppe (12): Dicarboximide (12-1) Captafol (bekannt aus US 3,178,447) der FormelGroup (12): Dicarboximides (12-1) Captafol (known from US 3,178,447) of the formula
(12-2) Folpet (bekannt aus US 2,553,770) der Formel (12-2) folpet (known from US 2,553,770) of the formula
(12-3) Iprodione (bekannt aus DE-A 21 49 923) der Formel(12-3) Iprodione (known from DE-A 21 49 923) of the formula
(12-4) Procymidone (bekannt aus DE-A 20 12 656) der Formel (12-4) procymidones (known from DE-A 20 12 656) of the formula
(12-5) Vinclozolin (bekannt aus DE-A 22 07 576) der Formel(12-5) Vinclozoline (known from DE-A 22 07 576) of the formula
Gruppe (13): GuanidineGroup (13): guanidines
(13-1) Dodine (bekannt aus GB 11 03 989) der Formel(13-1) Dodine (known from GB 11 03 989) of the formula
(13-2) Guazatine (bekannt aus GB 11 14 155) (13-3) Iminoctadine triacetate (bekannt aus EP-A 0 155 509) der Formel(13-2) guazatine (known from GB 11 14 155) (13-3) iminoctadine triacetate (known from EP-A 0 155 509) of the formula
Gruppe (14): ImidazoleGroup (14): imidazoles
(14-1) Cyazofamid (bekannt aus EP-A 0298 196) der Formel(14-1) Cyazofamide (known from EP-A 0298 196) of the formula
(14-2) Prochloraz (bekannt aus DE-A 2429 523) der Formel(14-2) Prochloraz (known from DE-A 2429 523) of the formula
(14-3) Triazoxide (bekannt aus DE-A 28 02488) der Formel (14-3) triazoxides (known from DE-A 28 02488) of the formula
(14-4) Pefurazoate (bekannt aus EP-A 0248 086) der Formel(14-4) Pefurazoate (known from EP-A 0248 086) of the formula
Gruppe (15): MoφholineGroup (15): Moφholine
(15-1) Aldimorph (bekannt aus DD 140 041) der Formel(15-1) Aldimorph (known from DD 140 041) of the formula
(15-2) Tridemorph (bekannt aus GB 988 630) der Formel(15-2) Tridemorph (known from GB 988 630) of the formula
(15-3) Dodemorph (bekannt aus DE-A 25 432 79) der Formel(15-3) Dodemorph (known from DE-A 25 432 79) of the formula
(15-4) Fenpropimorph (bekannt aus DE-A 2656747) der Formel(15-4) Fenpropimorph (known from DE-A 2656747) of the formula
Gruppe Hό): Pyrrole Group Hό): Pyrroles
(16-1) Fenpiclonil (bekannt aus EP-A 0 236 272) der Formel(16-1) Fenpiclonil (known from EP-A 0 236 272) of the formula
(16-2) Pyrrolnitrine (bekannt aus JP 65-25876) der Formel(16-2) pyrroline nitrines (known from JP 65-25876) of the formula
Gruppe (17V PhosphonateGroup (17V phosphonates
(17-1) Phosphonic acid (bekannte Chemikalie) der Formel(17-1) Phosphonic acid of the formula
Gruppe (18): Phenylethanamide (bekannt aus WO 96/23793, jeweils als E- oder Z-Isomer bevorzugt als E-Isomer)Group (18): phenylethanamides (known from WO 96/23793, in each case as E or Z isomer, preferably as E isomer)
(18-1) die Verbindung 2-(2,3-Dihydro-lH-inden-5-yl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(meth- oxyimino)acetamid der Formel(18-1) the compound 2- (2,3-dihydro-1H-inden-5-yl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxyimino) acetamide of the formula
(18-2) die Verbindung N-[2-(3,4-Dimethoxyphenyl)ethyl]-2-(methoxyimino)-2-(5,6,7,8-tetrahydro- naphthalen-2-yl)acetamid der Formel(18-2) the compound N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxyimino) -2- (5,6,7,8-tetrahydronaphthalen-2-yl) acetamide of the formula
(18-3) die Verbindung 2-(4-Chlθφhenyl)-N-[2-(3,4-dimeraoxyphenyl)ethyl]-2-(methoxyimino)acet- amid der Formel (18-3) the compound 2- (4-chloro-phenyl) -N- [2- (3,4-dimeroxyphenyl) ethyl] -2- (methoxyimino) acetamide of the formula
(18-4) die Verbindung 2-(4-Bromphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(methoxyimino)acet- amid der Formel(18-4) the compound 2- (4-bromophenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxyimino) acetamide of the formula
(18-5) die Verbindung 2-(4-Methylphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(metiioxyirnino)- acetamid der Formel (18-5) the compound 2- (4-methylphenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (metiioxyirnino) acetamide of the formula
(18-6) die Verbindung 2-(4-Ethylphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(methoxyimino)acet- amid der Formel(18-6) the compound 2- (4-ethylphenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxyimino) acetamide of the formula
Gruppe (19): FungizideGroup (19): Fungicides
(19-1) Acibenzolar-S-methyl (bekannt aus EP-A 0 313 512) der Formel(19-1) acibenzolar-S-methyl (known from EP-A 0 313 512) of the formula
(19-2) Edifenphos (bekannt aus DE-A 1493 736) der Formel (19-2) Edifenphos (known from DE-A 1493 736) of the formula
(19-3) Famoxadone (bekannt aus EP-A 0393 911) der Formel (19-3) Famoxadone (known from EP-A 0393 911) of the formula
(19-4) Oxadixyl (bekannt aus DE-A 30 30 026) der Formel(19-4) Oxadixyl (known from DE-A 30 30 026) of the formula
(19-5) Spiroxamine (bekannt aus DE-A 37 35 555) der Formel (19-5) spiroxamine (known from DE-A 37 35 555) of the formula
(19-6) Dithianon (bekannt aus JP-A 44-29464) der Formel(19-6) Dithianone (known from JP-A 44-29464) of the formula
(19-7) Metrafenone (bekannt aus EP-A 0 897 904) der Formel(19-7) Metrafenone (known from EP-A 0 897 904) of the formula
(19-8) Fenamidone (bekannt aus EP-A 0 629616) der Formel(19-8) Fenamidone (known from EP-A 0 629616) of the formula
(19-9) 2,3-DibutyI-6-chlor-thieno[2,3-d]pyrimidin-4(3H)on (bekannt aus WO 99/14202) der Formel(19-9) 2,3-Dibutyl-6-chlorothieno [2,3-d] pyrimidin-4 (3H) on (known from WO 99/14202) of the formula
(19-10) Probenazole (bekannt aus US 3,629,428) der Formel (19-10) sample azoles (known from US 3,629,428) of the formula
(19-11) Isoprothiolane (bekannt aus US 3,856,814) der Formel(19-11) isoprothiolanes (known from US 3,856,814) of the formula
(19-12) Kasugamycin (bekannt aus GB 1 094 567) der Formel (19-12) Kasugamycin (known from GB 1 094 567) of the formula
(19-13) Phthalide (bekannt aus JP-A 57-55844) der Formel(19-13) Phthalides (known from JP-A 57-55844) of the formula
(19-14) N-({4-[(Cyclopropylarnino)carbonyl]phenyl}sulfonyl)-2-methoxybenzamid der Formel(19-14) N - ({4 - [(Cyclopropylamino) carbonyl] phenyl} sulfonyl) -2-methoxybenzamide of the formula
(19-15) 2-(4-Chlorphenyl)-N- {2-[3-methoxy-4-(prop-2-in-l -yloxy)phenyl]ethyl} -2-(prop-2-in-l - yloxy)acetamid (bekannt aus WO 01/87822) der Formel(19-15) 2- (4-chlorophenyl) -N- {2- [3-methoxy-4- (prop-2-yn-1-yloxy) phenyl] ethyl} -2- (prop-2-yne) 1-yloxy) acetamide (known from WO 01/87822) of the formula
(19-16) Quinoxyfen (bekannt aus EP-A 0326 330) der Formel(19-16) Quinoxyfen (known from EP-A 0326 330) of the formula
(19-17) Proquinazid (bekannt aus WO 94/26722) der Formel (19-17) proquinazide (known from WO 94/26722) of the formula
Gruppe (20): (Thio)Harnstoff-Derivate (20-1) Pencycuron (bekannt aus DE-A 27 32257) der FormelGroup (20): (thio) urea derivatives (20-1) pencycuron (known from DE-A 27 32 257) of the formula
(20-2) Thiophanate-ethyl (bekannt aus DE-A 18 06 123) der Formel(20-2) Thiophanate-ethyl (known from DE-A 18 06 123) of the formula
Gruppe (21): AmideGroup (21): Amides
(21-1) Fenoxanil (bekannt aus EP-A 0262 393) der Formel(21-1) Fenoxanil (known from EP-A 0262 393) of the formula
(21 -2) Diclocymet (bekannt aus JP-A 7-206608) der Formel(21-2) Diclocymet (known from JP-A 7-206608) of the formula
Gruppe f22): TriazolopyrimidineGroup f22): triazolopyrimidines
(22-1) 5-Chlor-N-[fi5>2,2,2-trifluor-l-me%lethyl]-6-(2,4,6-trifluorphenyl)[l,2,4]triazolo[lJ5-a]- pyrimidin-7-amin (bekannt aus US 5,986,135) der Formel (22-1) 5-Chloro-N- [fi5> 2,2,2-trifluoro-1-methylol] -6- (2,4,6-trifluorophenyl) [l, 2,4] triazolo [l J 5-a] - pyrimidin-7-amine (known from US 5,986,135) of the formula
(22-2) 5-Chlor-N-[(7R>l,2-dime%lpropylJ-6-(2,4,6-trifluoφhenyl)[l,2,4]1xiazolo[l,5-a]pyrimidin- 7-amin (bekannt aus WO 02/38565) der Formel(22-2) 5-Chloro-N - [(7R> l, 2-dimethylpropylJ-6- (2,4,6-trifluorophenyl) [l, 2,4] 1Xiazolo [l, 5-a] pyrimidine - 7-amine (known from WO 02/38565) of the formula
(22-3) 5-Chlor-6<2-chlor-6-fluoiphenyl)-7-(4-me%lpiperidin-l-yl)[l,2,4]triazolo[l,5-a]pyrimidin (belcannt aus US 5,593,996) der Formel (22-3) 5-Chloro-6 <2-chloro-6-fluoro-phenyl) -7- (4-me% 1-piperidin-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine ( read from US 5,593,996) of the formula
(22-4) 5-Chlor-6-(2,4,6-trifluoφhenyl)-7-(4-methylpiperidin-l-yl)[l,2,4]triazolo[l,5-a]pyrimidin (bekannt aus DE-A 101 24208) der Formel(22-4) 5-Chloro-6- (2,4,6-trifluorophenyl) -7- (4-methylpiperidin-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine (known from DE-A 101 24208) of the formula
(22-5) 5-Chlor-6-(2,4,6-trifluoφhenyl)-N-[(iS)-l,2,2-rrimethylpropyl][l,2,4]triazolo[l,5-a]pyri din-7-amin (bekannt aus US 5,593,996) der Formel(22-5) 5-Chloro-6- (2,4,6-trifluorophenyl) -N - [(iS) -l, 2,2-trimethylpropyl] [l, 2,4] triazolo [1,6,5-a ] pyridine-7-amine (known from US 5,593,996) of the formula
Gruppe (23): IodochromoneGroup (23): iodochromones
(23-1) 2-Butoxy-6-iod-3-propyl-benzopyran-4-on (bekannt aus WO 03/014103) der Formel (23-1) 2-Butoxy-6-iodo-3-propyl-benzopyran-4-one (known from WO 03/014103) of the formula
(23-2) 2-Ethoxy-6-iod-3-propyl-benzopyran-4-on (bekannt aus WO 03/014103) der Formel(23-2) 2-Ethoxy-6-iodo-3-propyl-benzopyran-4-one (known from WO 03/014103) of the formula
(23-3) 6-Iod-2-propoxy-3-propyl-benzopyran-4-on (bekannt aus WO 03/014103) der Formel(23-3) 6-iodo-2-propoxy-3-propyl-benzopyran-4-one (known from WO 03/014103) of the formula
(23-4) 2-But-2-inyloxy-6-iod-3-propyl-benzopyran-4-on (bekannt aus WO 03/014103) der Formel(23-4) 2-But-2-ynyloxy-6-iodo-3-propyl-benzopyran-4-one (known from WO 03/014103) of the formula
(23-5) 6-Iod-2-(l-methyl-butoxy)-3-propyl-benzopyran-4-on (bekannt aus WO 03/014103) der Formel(23-5) 6-iodo-2- (1-methyl-butoxy) -3-propyl-benzopyran-4-one (known from WO 03/014103) of the formula
(23-6) 2-But-3-enyloxy-6-iod-benzopyran-4-on (bekannt aus WO 03/014103) der Formel(23-6) 2-But-3-enyloxy-6-iodobenzopyran-4-one (known from WO 03/014103) of the formula
(23-7) 3-Butyl-6-iod-2-isopropoxy-benzopyran-4-on (bekannt aus WO 03/014103) der Formel(23-7) 3-Butyl-6-iodo-2-isopropoxy-benzopyran-4-one (known from WO 03/014103) of the formula
Überraschenderweise ist die füngizide Wirkung der erfϊndungsgemäßen Wirkstoffkombinationen wesentlich höher als die Summe der Wirkungen der einzelnen Wirkstoffe. Es liegt also ein nicht vorhersehbarer, echter synergistischer Effekt vor und nicht nur eine Wirkungsergänzung. Die Verbindungen der Gruppe (1) sind durch die Formel (I) allgemein definiert.Surprisingly, the fungicidal activity of the active compound combinations according to the invention is significantly higher than the sum of the effects of the individual active compounds. So there is an unpredictable, true synergistic effect and not just an effect supplement. The compounds of group (1) are generally defined by the formula (I).
Bevorzugt sind Carboxamide der Formel (T), in welcherPreference is given to carboxamides of the formula (T) in which
R für Wasserstoff oder Methyl steht,R is hydrogen or methyl,
G für Wasserstoff oder Methyl steht,G is hydrogen or methyl,
R1 für Wasserstoff, Fluor, Chlor, Methyl, Ethyl, n-, iso-Propyl, Monofluormethyl, Difluor- methyl, Trifluormethyl, Monochlormethyl, Dichlormethyl oder Trichlormethyl steht, A für einen der folgenden Reste Al oder A2 steht:R 1 is hydrogen, fluorine, chlorine, methyl, ethyl, n-, iso-propyl, monofluoromethyl, difluoromethyl, trifluoromethyl, monochloromethyl, dichloromethyl or trichloromethyl, A is one of the following radicals Al or A2:
X für CH oder N steht, X is CH or N,
R2 für Methyl, Difluormethyl oder Trifluormethyl steht, R3 für Wasserstoff oder Fluor steht,R 2 is methyl, difluoromethyl or trifluoromethyl, R 3 is hydrogen or fluorine,
R für Difluormethyl oder Trifluormethyl steht.R is difluoromethyl or trifluoromethyl.
Die Formel (T) umfasst insbesondere die folgenden bevorzugten Mischungspartner der Gruppe (1):The formula (T) comprises in particular the following preferred mixing partners of group (1):
(1-1) N-[2-(l,3-Dimethylbutyl)-3-thienyl]4-metiiyl-3-(trifluormethyl)-lH-pyrazol-4-carboxamid(1-1) N- [2- (1,3-Dimethylbutyl) -3-thienyl] 4-methyl-3- (trifluoromethyl) -1H-pyrazole-4-carboxamide
(1-2) l-Methyl-3-(trifluormethyl)-N-[2<l>3,3-trime%lbu1yl)-3-thienyl]-lH-pyrazol-4-carboxamid(1-2) 1-Methyl-3- (trifluoromethyl) -N- [2 <3 > -trimine-1-butyl-3-thienyl] -H-pyrazole-4-carboxamide
(1-3) l-Me%l-N-[2^3-methylbutyl)-3-thienyl]-3-(trifluormethyl)--ffl-pyrazol-4-carboxamid(1-3) 1-Me-1-N- [2- (3-methylbutyl) -3-thienyl] -3- (trifluoromethyl) -f-pyrazole-4-carboxamide
(1-4) N-[2-(3,3-Dimethylbutyl)-3-tMenyl]4-methyl-3-(trifluormethyl)-lH-pyrazol-4-carboxamid (1-5) 3-(Pifluormethyl)-N42-(l,3-dimethylbuτyl)-3-thienyl]-l-me%l-lH-pyrazole^-carboxarnid(1-4) N- [2- (3,3-Dimethylbutyl) -3-t-mylyl] 4-methyl-3- (trifluoromethyl) -1H-pyrazole-4-carboxamide (1-5) 3- (pifluoromethyl) - N42 (l, 3-dimethylbuτyl) -3-thienyl] -l-me% l-lH-pyrazole ^ -carboxarnid
(1-6) 3-(Difluormethyl)-l-methyl-N-[2<l,3,3-1rime%lbutyl)-3-1iiienyl]4H-pyrazol-4-carboxamid(1-6) 3- (Difluoromethyl) -1-methyl-N- [2 <1,3,3-trimethylene-3-ylienyl] 4H-pyrazole-4-carboxamide
(1-7) 3-(Piflύoπnethyl)-l-me%l-N-[2-(3-memylbutyl)-3-thienyl]-lH-pyrazole-4-carboxamid(1-7) 3- (piflύoπnethyl) -l-me% 1-N- [2- (3-memylbutyl) -3-thienyl] -1H-pyrazole-4-carboxamide
(1-8) 3-(Difluoπnethyl)-N-[2-(3,3-dimethylbu1yl)-3-thienyl]4-memyl-lH-pyrazoM-carboxamid(1-8) 3- (Difluoromethyl) -N- [2- (3,3-dimethylbuyl) -3-thienyl] 4-memyl-1H-pyrazole-M-carboxamide
(1-9) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-5-fluor-l,3-dimethyl-lH-pyrazol-4-carboxamid (1-10) 5-Fluor-l,3-dimethyl-N-[2<l,3,3-1rimethylbutyl)-3-thienyl]-lH-pyrazol-4-carboxamid(1-9) N- [2- (1,3-Dimethylbutyl) -3-thienyl] -5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide (1-10) 5-fluoro-1 , 3-dimethyl-N- [2 <l, 3,3-1rimethylbutyl) -3-thienyl] -lH-pyrazole-4-carboxamide
(1-11) 5-Fluor-l,3-dimethyl-N-[2-(3-memylbutyl)-3-thienyl]-lH-pyrazol-4-carboxamid(1-11) 5-Fluoro-1,3-dimethyl-N- [2- (3-memylbutyl) -3-thienyl] -1H-pyrazole-4-carboxamide
(1-12) N-[2-(3,3-Dimethylbutyl)-3-thienyl]-5-fluor-l,3-dimethyl-lH-pyrazol-4-carboxamid(1-12) N- [2- (3,3-Dimethylbutyl) -3-thienyl] -5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide
(1-13) N-[2<l,3-Dimemylbutyl)-3-tMenyl]4-me%l-4<Mfluormethyl)-lH-ρyrrol-3-carboxamid(1-13) N- [2 <l, 3-Dimethylbutyl) -3-t-mensyl] 4-me% l-4 <Mfluoromethyl) -1H-ρyrrole-3-carboxamide
(1-14) l-Methyl-N-[2<3-methylbu1yl)-3-tMenyl]-3<trifluormethyl)-lH-pyrrol-4-carboxarnid (1-15) N-[2-(3,3-Dimethylbu1yl)-3-thienyl]4-methyl-3-(triiluormethyl)-lH-pyrrol-4-carboxamid(1-14) 1-Methyl-N- [2 <3-methylbulyl) -3-t-mylyl] -3 <trifluoromethyl) -1H-pyrrole-4-carboxamide (1-15) N- [2- (3,3 -Dimethylbu1yl) -3-thienyl] 4-methyl-3- (triiluormethyl) -lH-pyrrol-4-carboxamide
(1-16) N-[2-(3,3-Dimethylbutyl)-3-thienyl]4-memyl-3-(trifluorme%l)-lH-ρyrrol-4-carboxarnid(1-16) N- [2- (3,3-Dimethylbutyl) -3-thienyl] 4-memyl-3- (trifluoromethylene) -1H-pyrrol-4-carboxamide
(1-17) 4-(Difluormethyl)-N-[2-(l ,3-dimethylbutyl)-3-thienyl]-l -methyl-lH-pyrrol-3-carboxamid(1-17) 4- (Difluoromethyl) -N- [2- (1,3-dimethylbutyl) -3-thienyl] -1-methyl-1H-pyrrole-3-carboxamide
(1-18) 4-(Difluorme%l)4-me%l-N-[2-(l,3,3-trimethylbutyl)-3-thienyl]4H-pyrrol-3-carboxarnid (1-19) 4-(Difluormethyl)4-me%l-N-[2<3-methylbutyl)-3-thienyl]4H-pyirole-3-carboxamid (1-20) 4-(Difluorme%l)-N-[2-(3,3-dime%lbutyl)-3-thienyl]-l-methyl-lH-pyrrol-3-carboxamid (1-21) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-2-fluor-l?4-dimethyl-lH-pyrrol-3-carboxamid (1-22) 5-Fluor4,4-dime%l-N-[2-(l,3,3-irimethylbutyl)-3-thienyl]-lH-pyrrol-3-carboxamid (1-23) 5-Fluor-l,4-dimethyl-N-[2-(3-methylbutyl)-3-thienyl]-lH-pyrrol-3-carboxamid (1-24) N-[2-(353-Dime%lbutyl)-3-thienyl]-5-fluor-l,4-dimeihyl-lH-pyrrol-3-carboxamid (1-25) N-[2-(l53-Dimethylbutyl)-3-thienyl]-2-me%l-4-(trifluormethyl)-l,3-tiiiazol-5-carboxamid (1-26) 2-Me%l4-(trifluormethyl)-N-[2<l,3,3-trime1hylbutyl)-3-tMenyl]-l,3-thiazol-5-carboxamid (1-27) 2-Methyl-N-[2-(3-me%lbutyl)-3-tWenyl]^-(trifluormethyl)-l,3-thiazol-5-carboxamid (1-28) N-[2-(3,3-Dimethylbutyl)-3-thieny^^(1-18) 4- (Difluoroethylene) 4-me% LN- [2- (1,3,3-trimethylbutyl) -3-thienyl] 4H-pyrrole-3-carboxamide (1-19) 4- (Difluoromethyl) -4-me% 1N- [2 <3-methylbutyl) -3-thienyl] 4H-pyirole-3-carboxamide (1-20) 4- (difluoromethylene) -N- [2- (3,3-dime% butyl) -3-thienyl] -1-methyl-1H-pyrrole-3-carboxamide (1-21) N- [2- (1,3-dimethylbutyl) -3-thienyl ] -2-fluoro-L ? 4-dimethyl-1H-pyrrole-3-carboxamide (1-22) 5-fluoro4,4-dime% 1N- [2- (1,3,3-dimethylbutyl) -3-thienyl] -H-pyrrole-3-yl carboxamide (1-23) 5-Fluoro-1,4-dimethyl-N- [2- (3-methylbutyl) -3-thienyl] -1H-pyrrole-3-carboxamide (1-24) N- [2- (2- 3 5 3-Dime% lbutyl) -3-thienyl] -5-fluoro-l, 4-dimeihyl-lH-pyrrole-3-carboxamide (1-25) N- [2- (l 5 3-dimethylbutyl) -3 -thienyl] -2-me% l-4- (trifluoromethyl) -1,3-tiaziazole-5-carboxamide (1-26) 2-Me% l4- (trifluoromethyl) -N- [2 <l, 3.3 -trimethylbutyl) -3-t-methylenyl] -1,3-thiazole-5-carboxamide (1-27) 2-methyl-N- [2- (3-methylbutyl) -3-t-wyl] - (trifluoromethyl) - l, 3-thiazole-5-carboxamide (1-28) N- [2- (3,3-dimethylbutyl) -3-thienyl]
(1-29) 4-φifluoπnethyl)-N-[2-(l,3-dime%lbutyl)-3-thienyl]-2-methyl-l,3-thiazol-5-carboxamid (1-30) 4-pifluorme%l)-2-me%l-N-[2-(l,3,3-trimethylbutyl)-3-1hienyl]-l,3-1iiiazol-5-carboxamid (1-31) 4-(Difluormethyl)-2-me%l-N-[2-(3-methylbutyl)-3-thienyl]-l ,3-thiazol-5-carboxamid (1-32) 4-(Difluorme%l)-N-[2-(3,3-dimetliylbutyl)-3-tbienyl]-2-methyl-l,3-thiazol-5-carboxaπiid(1-29) 4-.phi-fluoro-ethyl) -N- [2- (1,3-dimethyl-1-butyl) -3-thienyl] -2-methyl-1,3-thiazole-5-carboxamide (1-30). pifluoromew% 1) -2-me% 1N- [2- (1,3,3-trimethylbutyl) -3-1hienyl] -1,3,1-thiazole-5-carboxamide (1-31) 4- (difluoromethyl) -2 -me% 1N- [2- (3-methylbutyl) -3-thienyl] -1,3-thiazole-5-carboxamide (1-32) 4- (difluoromethylene) -N- [2- (3,3 -dimetliylbutyl) -3-tbienyl] -2-methyl-l, 3-thiazol-5-carboxaπiid
Hervorgehoben sind erfindungsgemäße Wirkstoffkombinationen, die neben dem Carboxamid (1-1) N- [2-(l,3-Dimeihylbutyl)-3-iMenyl]-l-methyl-3-(trifluormethyl)-lH-pyrazol-4-carboxamid (Gruppe 1) einen oder mehrere, bevorzugt einen, Mischungspartner der Gruppen (2) bis (23) enthält.Highlighted are active compound combinations according to the invention which, in addition to the carboxamide (1-1), have N- [2- (1,3-dimethylbutyl) -3-i-mylanyl] -1-methyl-3- (trifluoromethyl) -1H-pyrazole-4-carboxamide (cf. Group 1) contains one or more, preferably one, mixing partner of groups (2) to (23).
Hervorgehoben sind erfindungsgemäße Wirkstoffkombinationen, die neben dem Carboxamid (1-9) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-5-fluor-l,3-dimethyl-lH-pyrazol-4-carboxamid (Gruppe 1) einen oder mehrere, bevorzugt einen, Mischungspartner der Gruppen (2) bis (23) enthält.Highlighted are active compound combinations according to the invention which, in addition to the carboxamide (1-9), have N- [2- (1,3-dimethylbutyl) -3-thienyl] -5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide ( Group 1) contains one or more, preferably one, mixing partner of groups (2) to (23).
Hervorgehoben sind erfϊndungsgemäße Wirkstoffkombinationen, die neben dem Carboxamid (1-13) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-l-methyl4-(trifluormethyl)-lH-pyrrol-3-carboxamid (Gruppe 1) einen oder mehrere, bevorzugt einen, Mischungspartner der Gruppen (2) bis (23) enthält.Highlighted are erfϊndungsgemäße drug combinations, in addition to the carboxamide (1-13) N- [2- (l, 3-dimethylbutyl) -3-thienyl] -1-methyl4- (trifluoromethyl) -1H-pyrrole-3-carboxamide (group 1 ) contains one or more, preferably one, mixing partner of groups (2) to (23).
Hervorgehoben sind erfindungsgemäße Wirkstoffkombinationen, die neben dem Carboxamid (1-25) N- [2-(l,3-Dime%lbutyl)-3-iMenyl]-2-memyl4-(trifluormemyl)-l,3-thiazol-5-carboxarmd (Gruppe 1) einen oder mehrere, bevorzugt einen, Mischungspartner der Gruppen (2) bis (23) enthält.Particular emphasis is given to active compound combinations according to the invention which, in addition to the carboxamide (1-25), have N- [2- (1,3-dimethyl-1-butyl) -3-i-enyl] -2-memyl4- (trifluoromethyl) -1,3-thiazole-5-one. carboxarmetal (group 1) contains one or more, preferably one, mixing partner of groups (2) to (23).
Die Verbindung (6-6) Carpropamid besitzt drei asymmetrische substituierte Kohlenstoffatome. Die Verbindung (6-7) kann daher als Gemisch von verschiedenen Isomeren oder auch in Form einer einzigen Komponente vorliegen. Besonders bevorzugt sind die Verbindungen (lS,3i?)-2,2-Dichlor-N- [(lR)-l-(4-chlorphenyl)ethyl]-l-ethyl-3-methylcyclopropancarboxamid der Formel The compound (6-6) carpropamid has three asymmetric substituted carbon atoms. The compound (6-7) may therefore be present as a mixture of different isomers or in the form of a single component. Particularly preferred are the compounds (IS, 3i?) - 2,2-dichloro-N- [(1R) -1- (4-chlorophenyl) ethyl] -1-ethyl-3-methylcyclopropanecarboxamide of the formula
(lR,3»S}-2,2-Dichlor-N-[(li?)-l-(4-chlorphenyl)ethyl]-l-ethyl-3-methylcyclopropancarboxamid der Formel(1R, 3S) -2,2-dichloro-N - [(li) -l- (4-chlorophenyl) ethyl] -1-ethyl-3-methylcyclopropanecarboxamide of the formula
Als Mischungspartner sind die folgenden Wirkstoffe der Gruppen (2) bis (23) bevorzugt: (2-1) Fluoxastrobin, (2-2) (2£)-2-(2-{[6-(3-Chlor-2-methylphenoxy)-5-fluor-4-pyrimidinyl]oxy}phenyl)- 2-(methoxyimino)-N-methylethanamid, (2-3) Trifloxystrobin, (2-4) (2£^-2-(Metb.oxyirnino)-N-methyl-2- (2-{[({(l^-l-[3-(trifluoπne%l)phenyl]e%liden}amino)oxy]me%l}ρhenyl)ethanarnid, (2-5) (2£)-2- (Methoxyiiruno)-N-methyl-2-{2-[(i^-(^^ amid, (2-7) 5-Methoxy-2-me%l-4-(2-{[({(l^-l-[3-(trifluoraie%l)phenyl]ethyliden}arnino)oxy]me- thyl}phenyl)-2,4-dihydro-3H-l,2,4-triazol-3-on, (2-8) Dimoxystrobin, (2-9) Picoxystrobm, (2-10) Pyra- clostrobin, (3-3) Propiconazole, (3-4) Difenoconazole, (3-6) Cyproconazole, (3-7) Ηexaconazole, (3-8) Penconazole, (3-9) Myclobutanil, (3-10) Tetraconazole, (3-13) Flusilazole, (3-15) Prothioconazole, (3-16) Fenbuconazole, (3-17) Tebuconazole, (3-21) Bitertanol, (3-22) Triadimenol, (3-23) Triadimefon, (3-12) Epoxiconazole, (3-19) Metconazole, (3-24) Fluquinconazole, (4-1) Dichlofluanid, (4-2) Tolylflu- anid, (5-1) Iprovalicarb, (5-2) Benthiavalicarb, (6-2) Boscalid, (6-4) Ethaboxam, (6-5) Fenhexamid, (6-6) Carpropamid, (6-7) 2-CUor-4-[(2-fluor-2-methylpropanoyl)amino]-NN--dimethylbenzamid, (6-8) Picobenzamid, (6-9) Zoxamide, (6-10) S^-Dichlor-Ν^-cyanoplienyl^sothiazol-S-carboxamid, (7-1) Mancozeb, (7-2) Maneb, (7-4) Propineb, (7-5) Thiram, (7-6) Zineb, (8-1) Benalaxyl, (8-2) Furalaxyl, (8-3) Benalaxyl-M, (9-1) Cyprodinil, (9-2) Pyrimethanil, (10-1) 6-Chlor-5-[(3,5-dimethylisoxazol-4-yl)- sulfonyl]-2,2-difluor-5Η-[l,3]dioxolo[4,5-fjbenzimidazol, (10-3) Carbendazim, (11-1) Propamocarb, (11-2) Propamocarb-hydrochloride, (11-3) Propamocarb-Fosetyl, (12-2) Folpet, (12-3) Iprodione, (12-4) Procymidone, (13-1) Dodine, (13-2) Guazatine, (13-3) Iminoctadine triacetate, (14-1) Cyazofamid, (14-2) Prochloraz, (14-3) Triazoxide, (15-4) Fenpropimorph, (17-1) Phosphonic acid, (19-1) Acibenzo- lar-S-methyl, (19-3) Famoxadone, (19-4) Oxadixyl, (19-5) Spiroxamine, (19-8) Fenamidone, (19-15) 2-(4-CUθφhenyl)-Ν-{2-[3-methoxy-4-(prop-2-in-l-yloxy)phenyl]ethyl}-2-(prop-2-in-l-yloxy)acetar^ (19-16) Quinoxyfen, (19-17) Proquinazid, (20-1) Pencycuron, (22-1) 5-Chlor-N-[(7S>2,2,2-trifluor-l- methyle%l]-6-(2,4,6-trifluoφhenyl)[l,2,4]1riazolo[l,5-a]pyrirmdin-7-arnin, (22-2) 5-Chlor-N-[(7i?)-l,2- dimethylpropyl]-6-(2,4,6-trifluorphenyl)[l,2,4]1riazolo[l,5-a]pyrirnidin-7-arnin, (22-4) 5-Chlor-6-(2,4,6- trifluoφhenyl)-7-(4-me%lpiperidin-l-yl)[l,2,4]1xiazolo[l,5-a]pyrirnidin, (22-5) 5-Chlor-6-(2,4,6-triflu- θφhenyl)-N-[(76)4,2,2-trimethylproρyl][l,2,4]triazolo[l,5-a]pyrimidin-7-amin, (23-1) 2-Butoxy-6-iod- 3-propyl-benzopyran-4-on, (23-2) 2-Ethoxy-6-iod-3-propyl-benzopyran-4-on, (23-3) 6-Iod-2-propoxy-3- propyl-benzopyran-4-on.The following active substances of groups (2) to (23) are preferred as mixing partners: (2-1) fluoxastrobin, (2-2) (2 lb) -2- (2 - {[6- (3-chloro-2-one] methylphenoxy) -5-fluoro-4-pyrimidinyl] oxy} phenyl) -2- (methoxyimino) -N-methylethaneamide, (2-3) trifloxystrobin, (2-4) (2β, -2- (metb.oxyirnino) -N-methyl-2- (2 - {[({(1-yl) [3- (trifluorominal) -phenyl] e-halo} amino) oxy] -methyl (1-yl) -phenyl) ethanamide, (2-5 ) (2 lb) -2- (methoxy) -N-methyl-2- {2 - [(i ^ - (^^ amide, (2-7) 5-methoxy-2-me% l-4- (2 - {[({(1-chloro-3- (trifluoroyl) -1-phenyl] ethylidene} arnino) oxy] methyl} phenyl) -2,4-dihydro-3H-1,2,4-triazole 3-one, (2-8) dimoxystrobin, (2-9) picoxystrobm, (2-10) pyra- clostrobin, (3-3) propiconazole, (3-4) difenoconazole, (3-6) cyproconazole, (3 -7) acexaconazole, (3-8) penconazole, (3-9) myclobutanil, (3-10) tetraconazole, (3-13) flusilazole, (3-15) prothioconazole, (3-16) fenbuconazole, (3- 17) Tebuconazole, (3-21) Bitertanol, (3-22) Triadimenol, (3-23) Triadimefon, (3-12) Epoxiconazole, (3-19) Metconazole, (3-24) Fluquinconazole, (4-1 ) D ichlofluanide, (4-2) tolylfluidide, (5-1) iprovalicarb, (5-2) benthiavalicarb, (6-2) boscalid, (6-4) ethaboxam, (6-5) fenhexamide, (6-6 ) Carpropamide, (6-7) 2-Cuor-4 - [(2-fluoro-2-methylpropanoyl) amino] -NN-dimethylbenzamide, (6-8) picobenzamide, (6-9) zoxamide, (6-10 ) S ^ -dichloro-Ν ^ -cyanoplienyl-sothiazole-S-carboxamide, (7-1) mancozeb, (7-2) maneb, (7-4) propyneb, (7-5) thiram, (7-6) Zineb, (8-1) benalaxyl, (8-2) furalaxyl, (8-3) benalaxyl-M, (9-1) cyprodinil, (9-2) pyrimethanil, (10-1) 6-chloro-5- [(3,5-dimethylisoxazol-4-yl) sulfonyl] -2,2-difluoro-5Η- [1,3] dioxolo [4,5-fjbenzimidazole, (10-3) carbendazim, (11-1) propamocarb , (11-2) propamocarb-hydrochloride, (11-3) propamocarb-fosetyl, (12-2) folpet, (12-3) iprodione, (12-4) procymidone, (13-1) dodine, (13- 2) guazatine, (13-3) iminoctadine triacetate, (14-1) cyazofamide, (14-2) prochlorazole, (14-3) triazoxide, (15-4) fenpropimorph, (17-1) phosphonic acid, (19 -1) acibenzolar-S-methyl, (19-3) famoxadone, (19-4) oxadixyl, (19-5) spiroxamine, (19-8 ) Fenamidone, (19-15) 2- (4-C0-fluorophenyl) -Ν- {2- [3-methoxy-4- (prop-2-yn-1-yloxy) phenyl] ethyl} -2- (prop-2 -in-1-yloxy) acetar ^ (19-16) quinoxyfen, (19-17) proquinazide, (20-1) pencycuron, (22-1) 5-chloro-N - [(7S> 2,2,2 trifluoro-1-methyl-1-chloro-1- (2,4,6-trifluorophenyl) [1,2,4] -1-riazolo [l, 5-a] pyrimidin-7-arnine, (22-2) 5-chloro -N - [(7i-1-l, 2-dimethylpropyl] -6- (2,4,6-trifluorophenyl) [l, 2,4] 1-riazolo [l, 5-a] pyrirnidine-7-arnine, (22 -4) 5-chloro-6- (2,4,6-trifluorophenyl) -7- (4-me% 1-piperidin-1-yl) [l, 2,4] 1-aziazolo [l, 5-a] pyrimidine, ( 22-5) 5-chloro-6- (2,4,6-trifluoromethane) θ-phenyl) -N - [(76) 4,2,2-trimethylpropyl] [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (23-1) 2-butoxy-6-iodo 3-propyl-benzopyran-4-one, (23-2) 2-ethoxy-6-iodo-3-propyl-benzopyran-4-one, (23-3) 6-iodo-2-propoxy-3-propyl benzopyran-4-one.
Als Mischungspartner sind die folgenden Wirkstoffe der Gruppen (2) bis (23) besonders bevorzugt: (2-1) Fluoxastrobin, (2-2) (2^-2-(2-{[6<3-CWor-2-methylphenoxy)-5-fluor-4-pyriinidinyl]oxy}phenyl)- 2-(methoxyinτino)-N-methylethanarnid, (2-3) Trifloxystrobin, (3-15) Prothioconazole, (3-17) Tebucon- azole, (3-21) Bitertanol, (3-22) Triadimenol, (3-24) Fluquinconazole, (4-1) Dichlofluanid, (4-2) Tolyl- fluanid, (5-1) Iprovalicarb, (6-5) Fenhexamid, (6-6) Carpropamid, (6-8) Picobenzamid, (7-4) Propineb, (8-3) Benalaxyl-M, (9-2) Pyrimethanil, (10-3) Carbendazim, (11-3) Propamocarb-Fosetyl, (12-3) Ipro- dione, (14-2) Prochloraz, (14-3) Triazoxide, (19-5) Spiroxamine, (19-15) 2-(4-Chlorphenyl)-Ν-{2-[3- methoxy-4-(prop-2-in-l-yloxy)phenyl]ethy]}-2-(prop-2-iα-l-yloxy)acetamid, (22-4) 5-Chlor-6-(2,4,6-tri- fluorphenyl)-7-(4-methylpiperidm-l-yl)[l,2,4]triazolo[l,5-a]pyrimidin, (22-5) 5-Chlor-6-(2,4,6-trifluor- phenyl)-N-[(i6)-l,2,2-trime%lpropyl][l,2,4]triazolo[l,5-a]pyrirnidin-7-aminThe following active substances of groups (2) to (23) are particularly preferred as mixing partners: (2-1) fluoxastrobin, (2-2) (2 ^ -2- (2 - {[6 <3-C-nor-2-methylphenoxy ) -5-fluoro-4-pyriaminidinyl] oxy} phenyl) -2- (methoxyquinone) -N-methylethanamide, (2-3) trifloxystrobin, (3-15) prothioconazole, (3-17) tebuconazole, (3 -21) bitertanol, (3-22) triadimenol, (3-24) fluquinconazole, (4-1) dichlorofluanide, (4-2) tolylfluoride, (5-1) iprovalicarb, (6-5) fenhexamide, ( 6-6) carpropamide, (6-8) picobenzamide, (7-4) propyneb, (8-3) benalaxyl-M, (9-2) pyrimethanil, (10-3) carbendazim, (11-3) propamocarbone Fosetyl, (12-3) iprodione, (14-2) prochloraz, (14-3) triazoxide, (19-5) spiroxamine, (19-15) 2- (4-chlorophenyl) -Ν- {2- [3-methoxy-4- (prop-2-yn-1-yloxy) phenyl] ethyl]} - 2- (prop-2-iα-1-yloxy) acetamide, (22-4) 5-chloro-6- (2,4,6-trifluorophenyl) -7- (4-methylpiperidm-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine, (22-5) 5-chloro-6 - (2,4,6-trifluorophenyl) -N - [(i6) -l, 2,2-trimethylpropyl] [l, 2,4] triazolo [l, 5-a] pyrirnidin-7-amine
Im Folgenden werden bevorzugte Wirkstoffkombinationen beschrieben, die aus zwei Gruppen von Wirkstoffen bestehen und jeweils wenigstens ein Carboxamid der Formel (I) (Gruppe 1) und wenigstens einen Wirkstoff der angegebenen Gruppe (2) bis (23) enthalten. Diese Kombinationen sind die Wirkstoffkombinatioήen A bis R.In the following, preferred active substance combinations are described which consist of two groups of active compounds and each contain at least one carboxamide of the formula (I) (group 1) and at least one active compound of the stated group (2) to (23). These combinations are the Wirkstoffkombinatioήen A to R.
Bevorzugt sind Wirkstoffkombinationen A bis R, worin das Carboxamid der Formel (T) (Gruppe 1) aus der folgenden Liste ausgewählt ist:Preferred are active compound combinations A to R, wherein the carboxamide of the formula (T) (group 1) is selected from the following list:
(1-1) Ν-[2-(l,3-Dimethylbu1yl)-3-thienyl]-l-me%l-3-(1rifluormethyl)-lH-pyrazol-4-carboxamid (1-3) l-Methyl-N-[2-(3-methylbutyl)-3-mienyl]-3-(trifluormethyl)-lH-pyrazol-4-carboxamid (1-5) 3-(pifluormethyl)-N-[2-(l,3-dime1hylbutyl)-3-thienyl]-l-methyl-lH-pyrazole-4-carboxamid (1-7) 3-(Difluormethyl)-l-methyl-N-[2-(3-methylbutyl)-3-thienyl]-lH-pyrazole-4-carboxamid (1-9) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-5-fluor-l,3-dimethyl-lH-pyrazol-4-carboxamid (1-11) 5-Fluor-l,3-dimethyl-N-[2-(3-methylbutyl)-3-thienyl]-lH-pyrazol-4-carboxamid (1-13) N-[2-(l,3-Dimethylburyl)-3-mienyl]-l-methyl-4-(trifluormethyl)-lH-pvrrol-3-carboxamid (1-15) N-[2-(3,3-Dimethylbutyl)-3-tMenyl]-l-me%l-3-(trifluorme%l)-lH-pyrrol-4-carboxamid (1-17) 4-(Difluoπnethyl)-N-[2-(l,3-dime%lbutyl)-3-thienyl]-l-methyl-lH-pyrrol-3-carboxamid (1-19) 4-φifluoπnethyl)-l-methyl-N-[2-(3-methylbutyl)-3-thienyl]-lH-pyrrole-3--carboxamid (1-21) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-2-fluor-l,4-dimethyl-lH-pyrrol-3-carboxamid (1-23) 5-Fluor-l,4-dimethyl-N-[2-(3-methylbutyl)-3-thienyl]-lH-pyrrol-3-carboxamid (1-25) N-[2-(li3-Dime%lbutyl)-3-thienyl]-2-methyl-4-(trifluormethyl)-l,3-thiazol-5-carboxamid (1-27) 2-Methyl-N-[2-(3-methylbutyl)-3-thienyl]-4-(trifluormethyl)-l;3-thiazol-5-carboxamid (1-29) 4-(Difluormethyl)-N-[2-(l,3-dimethylbutyl)-3-thienyl]-2-methyl-ls3-thiazol-5-carboxamid (1-31) 4-(Difluormethyl)-2-tnethyl-N-[2-(3-methylbutyl)-3-thienyl]-l ,3-thiazol-5-carboxamid(1-1) Ν- [2- (1,3-Dimethylbulyl) -3-thienyl] -1-methyl-1- (1-trifluoromethyl) -1H-pyrazole-4-carboxamide (1-3) 1-methyl -N- [2- (3-methylbutyl) -3-mienyl] -3- (trifluoromethyl) -1H-pyrazole-4-carboxamide (1-5) 3- (pifluoromethyl) -N- [2- (1,3 -dime-1-butylbutyl) -3-thienyl] -1-methyl-1H-pyrazole-4-carboxamide (1-7) 3- (difluoromethyl) -1-methyl-N- [2- (3-methylbutyl) -3-thienyl] -LH-pyrazole-4-carboxamide (1-9) N- [2- (1,3-dimethylbutyl) -3-thienyl] -5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide (1 -11) 5-Fluoro-1,3-dimethyl-N- [2- (3-methylbutyl) -3-thienyl] -1H-pyrazole-4-carboxamide (1-13) N- [2- (1,3 -Dimethylburyl) -3-mienyl] -1-methyl-4- (trifluoromethyl) -1H-p-pyrrole-3-carboxamide (1-15) N- [2- (3,3-dimethylbutyl) -3-t-mylyl] -1 -me% 1-3 (trifluoromethylene) -1-H-pyrrole-4-carboxamide (1-17) 4- (difluoromethyl) -N- [2- (1,3-dime% butyl) -3-thienyl] -l-methyl-1H-pyrrole-3-carboxamide (1-19) 4-φ-fluoro-ethyl) -1-methyl-N- [2- (3-methylbutyl) -3-thienyl] -1H-pyrrole-3-carboxamide (1-21) N - [2- (1,3-Dimethylbutyl) -3-thienyl] -2-fluoro-1,4-dimethyl-1H-pyrrole-3-carboxamide (1-23) 5-F luor-l, 4-dimethyl-N- [2- (3-methylbutyl) -3-thienyl] -lH-pyrrole-3-carboxamide (1-25) N- [2- (l i 3-Dime% lbutyl) 3-thienyl] -2-methyl-4- (trifluoromethyl) -1,3-thiazole-5-carboxamide (1-27) 2-methyl-N- [2- (3-methylbutyl) -3-thienyl] - 4- (trifluoromethyl) -1 ; 3-thiazol-5-carboxamide (1-29) 4- (difluoromethyl) -N- [2- (l, 3-dimethylbutyl) -3-thienyl] -2-methyl-l s 3-thiazol-5-carboxamide (1-31) 4- ( Difluoromethyl) -2-methyl-N- [2- (3-methylbutyl) -3-thienyl] -1,3-thiazole-5-carboxamide
Besonders bevorzugt sind Wirkstoffkombinationen A bis R, worin das Carboxamid der Formel (T) (Gruppe 1) aus der folgenden Liste ausgewählt ist:Particular preference is given to active ingredient combinations A to R in which the carboxamide of the formula (T) (group 1) is selected from the following list:
(1-1) N-[2-(l,3-Dimethylbu1yl)-3-thienylH(1-1) N- [2- (1,3-dimethylbubyl) -3-thienylH
(1-5) 3-(Difluoπnethyl)-N-[2-(l,3-dimethylbutyl)-3-thienyl]-l-methyl-lH-pyrazole-4-carboxarnid(1-5) 3- (Difluoromethyl) -N- [2- (1,3-dimethylbutyl) -3-thienyl] -1-methyl-1H-pyrazole-4-carboxamide
(1-9) N-[2-(l,3-Dimethylbu1yl)-3-thienyl]-5-fluor-l,3-dimethyl-lH-pyrazol-4-carboxamid(1-9) N- [2- (1,3-Dimethylbuyl) -3-thienyl] -5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide
(1-13) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-l-me%M<trifluoπnethyl)-m-pyrrol-3-carboxarnid(1-13) N- [2- (1,3-dimethylbutyl) -3-thienyl] -l-M% M <trifluoromethyl) -m-pyrrole-3-carboxamide
(1-17) 4-(pifluoπnethyl)-N-[2-(l,3-dimethylbu1yl)-3-thienyl]4-metiiyl4H-pyrrol-3-carboxarrad(1-17) 4- (pifluoromethyl) -N- [2- (1,3-dimethyl-butyl) -3-thienyl] -4-methyl-4H-pyrrole-3-carboxaric
(1-21) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-2-fluor-l,4-dimethyl-lH-pyrrol-3-carboxarnid(1-21) N- [2- (1,3-dimethylbutyl) -3-thienyl] -2-fluoro-1,4-dimethyl-1H-pyrrole-3-carboxamide
(1-25) N-[2-(l,3-Dimethylbutyl)-3-thienyl]-2-me1hyl-4<ttfluormethyl)4,3-thiazol-5-carboxarnid(1-25) N- [2- (1,3-Dimethylbutyl) -3-thienyl] -2-methyl-4-t-fluoromethyl) 4,3-thiazole-5-carboxamide
(1-29) 4-(Difluormethyl)-N-[2~(l ,3-dimethylbutyl)-3-thienyl]-2-methyl-l ,3-thiazol-5-carboxamid(1-29) 4- (Difluoromethyl) - N - [2- (1,3-dimethylbutyl) -3-thienyl] -2-methyl-1,3-thiazole-5-carboxamide
Bevorzugt sind Wirkstoff kombinationen A, worin das Strobilurin (Gruppe 2) aus der folgenden Liste ausgewählt ist: (2-1) Fluoxastrobin, (2-2) (2£)-2-(2-{[6-(3-Chlor-2-methylphenoxy)-5-fluor-4-pyrimidi- nyl]oxy}phenyl)-2-(memoxyimino)-N-methylethanamid, (2-3) Trifloxystrobin, (2-4) (2E)-2-(Methoxy- imino)-N-methyl-2-(2-{[({(li^-l-[3-(1rifluorm amid, (2-5) (2^-2-(Methoxvirmno)-N-memyl-2-{2-[(^-({l-[3-(1rifluoπne%l)phenyl]ethoxy}irriino)- methyl]phenyl}ethanamid, (2-6) Orysastrobin, (2-7) 5-Methoxy-2-me%l-4-(2-{[({(l£)-l-[3-(trifluor- me1hyl)phenyl]ethyliden}amino)oxy]meliiyl}phenyl)-2,4-dih.ydro-3H-l,2,4-triazol-3-on, (2-8) Dimoxy- strobin, (2-9) Picoxystrobin, (2-10) Pyraclostrobin.Preferred are drug combinations A wherein the strobilurin (Group 2) is selected from the following list: (2-1) fluoxastrobin, (2-2) (2E) -2- (2 - {[6- (3-chloro 2-methylphenoxy) -5-fluoro-4-pyrimidinyl] oxy} phenyl) -2- (memoxyimino) -N-methylethanamide, (2-3) trifloxystrobin, (2-4) (2E) -2- ( Methoxy-imino) -N-methyl-2- (2 - {[({(li) -l- [3- (1-fluoro-amide, (2-5) (2 ^ -2- (methoxy) -N-memyl) 2- {2 - [(^ - ({1- [3- (1-fluoro-1%) -phenyl] -ethoxy} -irrino) -methyl] -phenyl} -ethaneamide, (2-6) orysastrobin, (2-7) 5-methoxy- 2-me% l-4- (2 - {[({(l) -l- [3- (trifluoromethyl) phenyl] ethylidene} amino) oxy] meliiyl} phenyl) -2,4-dihydroxy -3H-l, 2,4-triazol-3-one, (2-8) dimoxy-strobine, (2-9) picoxystrobin, (2-10) pyraclostrobin.
Besonders bevorzugt sind Wirkstofikombinationen A, worin das Strobilurin (Gruppe 2) aus der folgenden Liste ausgewählt ist: (2-1) Fluoxastrobin, (2-2) (2£)-2-(2-{[6-(3-Chlor-2-methylphenoxy)- 5-fluor-4-pyrirnidinyl]oxy}phenyl)-2-(memoxyirnino)-N-methylethanamid, (2-3) Trifloxystrobin, (2- 8) Dimoxystrobin, (2-9) Picoxystrobin, (2-10) Pyraclostrobin.Particularly preferred are drug combinations A wherein the strobilurin (Group 2) is selected from the following list: (2-1) fluoxastrobin, (2-2) (2E) -2- (2 - {[6- (3-chloro -2-methylphenoxy) - 5-fluoro-4-pyrirnidinyl] oxy} phenyl) -2- (memoxy-imino) -N-methylethanamide, (2-3) trifloxystrobin, (2-8) dimoxystrobin, (2-9) picoxystrobin, (2-10) Pyraclostrobin.
Hervorgehoben sind die in der folgenden Tabelle 1 angeführten Wirkstoffkombinationen A: Tabelle 1: Wirkstoffkombinationen AHighlighted are the active substance combinations A listed in Table 1 below: TABLE 1 Active substance combinations A
Tabelle 1: Wirkstoffkombinationen A Table 1: Active substance combinations A
Bevorzugt sind Wirkstoffkombinationen B, worin das Triazol (Gruppe 3) aus der folgenden Liste ausgewählt ist: (3-1) Azaconazole, (3-2) Etaconazole, (3-3) Propiconazole, (3-4) Difenoconazole, (3-5) Bromuconazole, (3-6) Cyproconazole, (3-7) Hexaconazole, (3-8) Penconazole, (3-9) Myclobutanil, (3-10) Tetraconazole, (3-11) Flutriafol, (3-12) Epoxiconazole, (3-13) Flusilazole, (3-14) Simeconazole, (3-15) Prothioconazole, (3-16) Fenbuconazole, (3-17) Tebuconazole, (3-18) Ipconazole, (3-19) Metcon- azole, (3-20) Triticonazole, (3-21) Bitertanol, (3-22) Triadimenol, (3-23) Triadimefon, (3-24) Fluquin- conazole, (3-25) Quinconazole.Preferred combinations of active compounds B are those in which the triazole (group 3) is selected from the following list: (3-1) azaconazoles, (3-2) etaconazoles, (3-3) propiconazoles, (3-4) difenoconazoles, (3 5) bromuconazoles, (3-6) cyproconazoles, (3-7) hexaconazoles, (3-8) penconazoles, (3-9) myclobutanil, (3-10) tetraconazoles, (3-11) flutriafol, (3-12 ) Epoxiconazoles, (3-13) flusilazoles, (3-14) simeconazoles, (3-15) prothioconazoles, (3-16) fenbuconazoles, (3-17) tebuconazoles, (3-18) ipconazoles, (3-19) Metcon- azoles, (3-20) triticonazole, (3-21) bitertanol, (3-22) triadimenol, (3-23) triadimefon, (3-24) fluquinconazole, (3-25) quinconazole.
Besonders bevorzugt sind Wirkstofßcombinationen B, worin das Triazol (Gruppe 3) aus der folgen- den Liste ausgewählt ist: (3-3) Propiconazole, (3-4) Difenoconazole, (3-6) Cyproconazole, (3-7) Hexaconazole, (3-15) Prothioconazole, (3-17) Tebuconazole, (3-19) Metconazole, (3-21) Bitertanol, (3-22) Triadimenol, (3-24) Fluquinconazole.Particularly preferred are drug combinations B wherein the triazole (group 3) is selected from the following list: (3-3) propiconazoles, (3-4) difenoconazoles, (3-6) cyproconazoles, (3-7) hexaconazoles, (3-15) prothioconazole, (3-17) tebuconazole, (3-19) metconazole, (3-21) bitertanol, (3-22) triadimenol, (3-24) fluquinconazole.
Hervorgehoben sind die in der folgenden Tabelle 2 angeführten Wirkstofflcombinationen B: Tabelle 2: Wirkstoffkombinationen BHighlighted are the drug combinations B listed in Table 2 below: TABLE 2 Active ingredient combinations B
Tabelle 2: Wirkstoffkombinationen B Table 2: Drug combinations B
Bevorzugt sind Wirkstoffkombinationen C, worin das Sulfenamid (Gruppe 4) aus der folgenden Liste ausgewählt ist: (4-1) Dichlofluanid, (4-2) Tolylfluanid.Preferred combinations of active compounds are C, in which the sulfenamide (group 4) is selected from the following list: (4-1) dichlorofluanide, (4-2) tolylfluanid.
Hervorgehoben sind die in der folgenden Tabelle 3 angeführten Wirkstoffkombinationen C: Tabelle 3: Wirkstoffkombinationen CHighlighted are the active ingredient combinations C listed in Table 3 below: Table 3: Drug combinations C
Bevorzugt sind Wirkstoffkombinationen D, worin das Valinamid (Gruppe 5) aus der folgenden Liste ausgewählt ist: (5-1) Iprovalicarb, (5-3) Benthiavalicarb.Preferred are active ingredient combinations D wherein the valinamide (group 5) is selected from the following list: (5-1) iprovalicarb, (5-3) benthiavalicarb.
Hervorgehoben sind die in der folgenden Tabelle 4 angeführten Wirkstoffkombinationen D: Tabelle 4: Wirkstoffkombinationen DHighlighted are the active ingredient combinations D listed in Table 4 below: TABLE 4 Active ingredient combinations D
Bevorzugt sind Wirkstoffkombinationen E, worin das Carboxamid (Gruppe 6) aus der folgenden Liste ausgewählt ist: (6-1) 2-Chloro-N-(l,l,3-trimethyl-indan-4-yl)-nicotinamid, (6-2) Boscalid, (6-3) Furametpyr, (6-4) Ethaboxam, (6-5) Fenhexamid, (6-6) Carpropamid, (6-7) 2-Chlor-4-(2-fluor-2-me- thyl-propionylamino)-N,N-dimethyl-benzamid, (6-8) Picobenzamid, (6-9) Zoxamide, (6-10) 3,4-Di- chlor-N-(2-cyanophenyl)isothiazol-5-carboxamid, (6-11) Carboxin, (6-12) Tiadinil, (6-13) Silthiofam. Besonders bevorzugt sind Wirkstoffkombinationen E, worin das Carboxamid (Gruppe 6) aus der folgenden Liste ausgewählt ist: (6-2) Boscalid, (6-4) Ethaboxam, (6-5) Fenhexamid, (6-6) Carprop- amid, (6-7) 2-Chlor-4-(2-fluor-2-methyl-propionylamino)-N,N-dimethyl-benzamid, (6-8) Picobenz- amid, (6-9) Zoxamide, (6-10) 3,4-Dichlor-N-(2-cyanophenyl)isothiazol-5-carboxamid.Preference is given to combinations of active substances E in which the carboxamide (group 6) is selected from the following list: (6-1) 2-chloro-N- (1,1,3-trimethyl-indan-4-yl) -nicotinamide, (6 -2) boscalid, (6-3) furametpyr, (6-4) ethaboxam, (6-5) fenhexamide, (6-6) carpropamide, (6-7) 2-chloro-4- (2-fluoro-2 -methyl-propionylamino) -N, N-dimethylbenzamide, (6-8) picobenzamide, (6-9) zoxamides, (6-10) 3,4-dichloro-N- (2-cyanophenyl) isothiazole-5-carboxamide, (6-11) carboxyne, (6-12) tiadinil, (6-13) silthiofam. Particular preference is given to combinations of active substances E in which the carboxamide (group 6) is selected from the following list: (6-2) boscalid, (6-4) ethaboxam, (6-5) fenhexamide, (6-6) carpropamide, (6-7) 2-Chloro-4- (2-fluoro-2-methylpropionylamino) -N, N-dimethylbenzamide, (6-8) picobenzamide, (6-9) zoxamide, (6- 10) 3,4-dichloro-N- (2-cyanophenyl) isothiazole-5-carboxamide.
Ganz besonders bevorzugt sind Wirkstoffkombinationen E, worin das Carboxamid (Gruppe 6) aus der folgenden Liste ausgewählt ist: (6-2) Boscalid, (6-5) Fenhexamid, (6-6) Carpropamid, (6-8) Picobenzamid.Very particular preference is given to combinations of active substances E in which the carboxamide (group 6) is selected from the following list: (6-2) boscalid, (6-5) fenhexamide, (6-6) carpropamide, (6-8) picobenzamide.
Hervorgehoben sind die in der folgenden Tabelle 5 angeführten Wirkstoffkombinationen E: Tabelle 5: Wirkstoffkombinationen EHighlighted are the active ingredient combinations E listed in Table 5 below: TABLE 5 Active ingredient combinations E
Bevorzugt sind Wirkstoffkombinationen F, worin das Dithiocarbamat (Gruppe 7) aus der folgenden Liste ausgewählt ist: (7-1) Mancozeb, (7-2) Maneb, (7-4) Propineb, (7-5) Thiram, (7-6) Zineb. Besonders bevorzugt sind Wirkstoffkombinationen F, worin das Dithiocarbamat (Gruppe 7) aus der folgenden Liste ausgewählt ist: (7-1) Mancozeb, (7-4) Propineb.Preferred active ingredient combinations are F, wherein the dithiocarbamate (group 7) is selected from the following list: (7-1) mancozeb, (7-2) maneb, (7-4) propineb, (7-5) thiram, (7 6) Zineb. Especially preferred are drug combinations F wherein the dithiocarbamate (group 7) is selected from the following list: (7-1) mancozeb, (7-4) propineb.
Hervorgehoben sind die in der folgenden Tabelle 6 angeführten Wirkstoffkombinationen F: Tabelle 6: Wirkstoffkombinationen FHighlighted are the active ingredient combinations F listed in Table 6 below: Table 6: Active substance combinations F
Bevorzugt sind Wirkstoffkombinationen G, worin das Acylalanin (Gruppe 8) aus der folgenden Liste ausgewählt ist: (8-1) Benalaxyl , (8-2) Furalaxyl, (8-5) Benalaxyl-M.Preferred are active ingredient combinations G wherein the acylalanine (group 8) is selected from the following list: (8-1) benalaxyl, (8-2) furalaxyl, (8-5) benalaxyl-M.
Besonders bevorzugt sind Wirkstoffkombinationen G, worin das Acylalanin der Formel (VT) (Gruppe 8) aus der folgenden Liste ausgewählt ist: (8-5) Benalaxyl-M.Particular preference is given to active ingredient combinations G in which the acylalanine of the formula (VT) (group 8) is selected from the following list: (8-5) benalaxyl-M.
Hervorgehoben sind die in der folgenden Tabelle 7 angeführten Wirkstoffkombinationen G: Tabelle 7: Wirkstoffkombinationen GHighlighted are the active ingredient combinations G listed in Table 7 below: TABLE 7 Active ingredient combinations G
Bevorzugt sind Wirkstoffkombinationen H, worin das Anilino-pyrimidin (Gruppe 9) aus der folgenden Liste ausgewählt ist: (9-1) Cyprodinü, (9-2) Pvrimethanil.Preferred combinations of active compounds are H, wherein the anilino-pyrimidine (group 9) is selected from the following list: (9-1) cyprodine, (9-2) pyrimethanil.
Hervorgehoben sind die in der folgenden Tabelle 8 angeführten Wirkstoffkombinationen H: Tabelle 8: Wirkstoffkombinationen HHighlighted are the active ingredient combinations H listed in Table 8 below: Table 8: Drug combinations H
Bevorzugt sind Wirkstoffkombinationen I, worin das Benzimidazol (Gruppe 10) aus der folgenden Liste ausgewählt ist: (10-1) 6-Chlor-5-[(3,5-dimethylisoxazol-4-yl)sulfonyl]-2,2-difluor-5H-[l,3]di- oxolo[4,5-f]benzimidazol, (10-2) Benomyl , (10-3) Carbendazim , (10-4) Chlorfenazole, (10-5) Fube- ridazole, (10-6) Thiabendazole.Preferred are active compound combinations I in which the benzimidazole (group 10) is selected from the following list: (10-1) 6-chloro-5 - [(3,5-dimethylisoxazol-4-yl) sulfonyl] -2,2-difluoro -5H- [1,3] dioxolo [4,5-f] benzimidazole, (10-2) benomyl, (10-3) carbendazim, (10-4) chlorfenazoles, (10-5) furfuridazoles, (10-6) Thiabendazoles.
Besonders bevorzugt sind Wirkstoffkombinationen I, worin das Benzimidazol der Formel (VID) (Gruppe 10) ist: (10-3) Carbendazim.Particularly preferred are drug combinations I, wherein the benzimidazole of the formula (VID) (group 10) is: (10-3) carbendazim.
Hervorgehoben sind die in der folgenden Tabelle 9 angeführten Wirkstoffkombinationen I: Tabelle 9: Wirkstoffkombinationen IHighlighted are the active ingredient combinations I listed in Table 9 below: TABLE 9 Active ingredient combinations I
Bevorzugt sind Wirkstoffkombinationen J, worin das Carbamat (Gruppe 11) aus der folgenden Liste ausgewählt ist: (11-1) Propamocarb, (11-2) Propamocarb-hydrochloride, (11-3) Propamocarb-Fosetyl.Preferred are active ingredient combinations J, wherein the carbamate (group 11) is selected from the following list: (11-1) propamocarb, (11-2) propamocarb-hydrochloride, (11-3) propamocarb-fosetyl.
Hervorgehoben sind die in der folgenden Tabelle 10 angeführten Wirkstoffkombinationen J: Tabelle 10: Wirkstoffkombinationen JHighlighted are the active ingredient combinations J listed in Table 10 below: Table 10: Drug combinations J
Bevorzugt sind Wirkstoffkombinationen K, worin das Dicarboximid (Gruppe 12) aus der folgenden Liste ausgewählt ist: (12-2) Folpet, (12-3) Iprodione.Preferred active ingredient combinations are K, wherein the dicarboximide (group 12) is selected from the following list: (12-2) folpet, (12-3) iprodione.
Hervorgehoben sind die in der folgenden Tabelle 11 angeführten Wirkstoffkombinationen K: Tabelle 11: Wirkstoffkombinationen KHighlighted are the active ingredient combinations K listed in Table 11 below: TABLE 11 Active ingredient combinations K
Bevorzugt sind Wirkstoffkombinationen L, worin das Guanidin (Gruppe 13) aus der folgenden Liste ausgewählt ist: (13-1) Dodine, (13-2) Guazatine. Preferred are active ingredient combinations L, wherein the guanidine (group 13) is selected from the following list: (13-1) dodine, (13-2) guazatine.
Hervorgehoben sind die in der folgenden Tabelle 12 angeführten Wirkstoffkombinationen L: Tabelle 12: Wirkstoffkombinationen LHighlighted are the active ingredient combinations L listed in Table 12 below: TABLE 12 Active ingredient combinations L
Bevorzugt sind Wirkstoffkombinationen M, worin das Imidazol (Gruppe 14) aus der folgenden Liste ausgewählt ist: (14-2) Prochloraz, (14-3) Triazoxide.Preferred are active ingredient combinations M, wherein the imidazole (group 14) is selected from the following list: (14-2) prochlorazole, (14-3) triazoxide.
Hervorgehoben sind die in der folgenden Tabelle 13 angeführten Wirkstoffkombinationen M: Tabelle 13: Wirkstoffkombinationen MHighlighted are the active ingredient combinations M listed in Table 13 below: TABLE 13 Active ingredient combinations M
Bevorzugt sind Wirkstoffkombinationen N, worin das Morpholin (Gruppe 15) aus der folgenden Liste ausgewählt ist: (15-1) Aldimorph, (15-2) Tridemorph, (15-3) Dodemorph, (15-4) Fenpropimorph. Besonders bevorzugt sind Wirkstoffkombinationen N, worin das Morpholin (Gruppe 15) aus der folgenden Liste ausgewählt ist: (15-4) Fenpropimorph.Preferred combinations of active agents are N, wherein the morpholine (group 15) is selected from the following list: (15-1) aldimorph, (15-2) tridemorph, (15-3) dodemorph, (15-4) fenpropimorph. Particularly preferred are drug combinations N, wherein the morpholine (group 15) is selected from the following list: (15-4) fenpropimorph.
Hervorgehoben sind die in der folgenden Tabelle 14 angeführten Wirkstoffkombinationen N: Tabelle 14: Wirkstofflcombinationen NHighlighted are the drug combinations N listed in Table 14 below: Table 14: Drug combinations N
Bevorzugt sind Wirkstoffkombinationen O, worin das Fungizid (Gruppe 19) aus der folgenden Liste ausgewählt ist: (19-1) Acibenzolar-S-methyl, (19-3) Famoxadone, (19-4) Oxadixyl, (19-5) Spirox- amine, (19-8) Fenamidone, (19-14) N-({4-[(Cyclopropylamino)carbonyl]phenyl}sulfonyl)-2-meth- oxybenzamid, (19-15) 2-(4-Chloφhenyl)-N-{2-[3-methoxy-4-(prop-2-in-l-yloxy)phenyl]ethyl}-2- (prop-2-in- 1 -yloxy)acetamid.Preferred combinations of active compounds are O, wherein the fungicide (group 19) is selected from the following list: (19-1) acibenzolar-S-methyl, (19-3) famoxadone, (19-4) oxadixyl, (19-5) spirox - amines, (19-8) fenamidone, (19-14) N - ({4 - [(cyclopropylamino) carbonyl] phenyl} sulfonyl) -2-methoxybenzamide, (19-15) 2- (4-chlorophenyl) -N- {2- [3-methoxy-4- (prop-2-yn-1-yloxy) phenyl] ethyl} -2- (prop-2-yn-1-ylxy) acetamide.
Besonders bevorzugt sind Wirkstoffkombinationen O, worin das Fungizid (Gruppe 19) aus der folgenden Liste ausgewählt ist: (19-5) Spiroxamine, (19-14) N-({4-[(Cyclopropylamino)carbonyi]- phenyl} sulfonyl)-2-methoxybenzamid, (19-15) 2-(4-Chlorphenyl)-N- {2-[3 -methoxy-4-(prop-2-in-l - yloxy)phenyl]ethyl} -2-(prop-2-in- 1 -yloxy)acetamid.Particular preference is given to active ingredient combinations O in which the fungicide (group 19) is selected from the following list: (19-5) spiroxamine, (19-14) N - ({4 - [(cyclopropylamino) carbonyl] -phenyl} sulfonyl) - 2-methoxybenzamide, (19-15) 2- (4-chlorophenyl) -N- {2- [3-methoxy-4- (prop-2-yn-1-yloxy) phenyl] ethyl} -2- (propyl) 2-in-1-oxy) acetamide.
Hervorgehoben sind die in der folgenden Tabelle 15 angeführten Wirkstoffkombinationen O: Tabelle 15: Wirkstoffkombinationen OHighlighted are the drug combinations O listed in Table 15 below: Table 15: Active ingredient combinations O
Tabelle 15: Wirkstoffkombinationen O Table 15: Active ingredient combinations O
Bevorzugt sind Wirkstoffkombinationen P, worin das (Thio)Harnstoff-Derivat (Gruppe 20) aus der folgenden Liste ausgewählt ist: (20-1) Pencycuron.Preferred are active ingredient combinations P, wherein the (thio) urea derivative (group 20) is selected from the following list: (20-1) pencycuron.
Hervorgehoben sind die in der folgenden Tabelle 16 angeführten Wirkstoffkombinationen P: Tabelle 16: Wirkstoffkombinationen PHighlighted are the active ingredient combinations P listed in Table 16 below: Table 16: Active substance combinations P
Bevorzugt sind Wirkstoffkombinationen Q, worin das Triazolopyrimidin (Gruppe 22) aus der folgenden Liste ausgewählt ist: (22-1) 5-Chlor-N-[(75>2,2,2-trifiuor-l-methylethyl]-6-(2,4,6-trifluorphe- nyl)[l ,2,4]triazolo[l ,5-a]pyrimidin-7-amin, (22-2) 5-Chlor-N-[(7i?>l ,2-dimethylpropyl]-6-(2,4,6-tri- fluorphenyl)[l,2,4]triazolo[l,5-a]pyrimidm-7-amin, (22-3) 5-Chlor-6-(2-chlor-6-fluorphenyl)-7-(4- methylpiperidin-l-yl)[l,2,4]triazolo[l,5-a]pyrimidin, (22-4) 5-Chlor-6-(2,4,6-trifluorphenyl)-7-(4-me- thylpiperidin-1 -yl)[l ,2,4]triazolo[l ,5-a]pyrimidin. Besonders bevorzugt sind Wirkstoffkombinationen Q, worin das Triazolopyrimidin (Gruppe 22) aus der folgenden Liste ausgewählt ist: (22-1) 5-Chlor-N-[f2S>2,2,2-trifluor-l-methylethyl]-6-(2,4,6- trifluoφhenyl)[l,2,4]triazolo[l,5-a]pyrimidin-7-amin, (22-2) 5-Chlor-N-[(7i?;-l,2-dimethylpropyl]-6- (2,4,6-trifluorphenyl)[l,2,4]triazolo[l,5-a]pyrimidin-7-amin, (22-4) 5-Chlor-6-(2,4,6-trifluorphenyl)- 7-(4-methylpiperidm-l-yl)[l,2,4]triazolo[l,5-a]pyrimidin, (22-5) 5-Chlor-6-(2,4,6-trifluorphenyl)-N- [(i5)-l,2,2-1rirnethylpropyl3[l,2,4]triazolo[l,5-a]pyrirffldin-7-amin.Preferred combinations of active compounds Q are those wherein the triazolopyrimidine (group 22) is selected from the following list: (22-1) 5-chloro-N - [(75,2,2,2-trifluoro-1-methylethyl) -6- ( 2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-2) 5-chloro- N - [(7i?> L, 2 -dimethylpropyl] -6- (2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-3) 5-chloro-6- ( 2-chloro-6-fluorophenyl) -7- (4-methylpiperidin-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine, (22-4) 5-chloro-6- (2 , 4,6-trifluorophenyl) -7- (4-methylpiperidin-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine. Particularly preferred are combinations of active ingredients Q, wherein the triazolopyrimidine (group 22) is selected from the following list: (22-1) 5-chloro-N- [f 2 S> 2,2,2-trifluoro-1-methylethyl] -6- ( 2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-2) 5-chloro-N - [(7i-1, 2- dimethylpropyl] -6- (2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-4) 5-chloro-6- (2,4 , 6-trifluorophenyl) - 7- (4-methylpiperidm-1-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine, (22-5) 5-chloro-6- (2,4, 6-trifluorophenyl) -N- [(i5) -l, 2,2,1-trimethylpropyl3 [l, 2,4] triazolo [l, 5-a] pyrrolidine-7-amine.
Hervorgehoben sind die in der folgenden Tabelle 17 angeführten Wirkstofflcombinationen Q: Tabelle 17; WirkstoffkombinationenHighlighted are the drug combinations Q listed in Table 17 below: Table 17; drug combinations
Tabelle 17: Wirkstoffkombinationen Table 17: Active ingredient combinations
Bevorzugt sind Wirkstoffkombinationen R, worin das Iodochromon (Gruppe 23) aus der folgenden Liste ausgewählt ist: (23-1) 2-Butoxy-6-iod-3rpropyl-benzoρyran-4-on, (23-2) 2-Ethoxy-6-iod-3- propyl-benzopyran-4-on, (23-3) 6-Iod-2-propoxy-3-propyl-benzopyran-4-on, (23-4) 2-But-2-inyloxy- 6-iod-3-propyl-benzoρyran-4-on, (23-5) 6-Iod-2-(l-methyl-butoxy)-3-propyl-benzopyran-4-on, (23-6) 2-But-3-enyloxy-6-iod-benzopyran-4-on, (23-7) 3-Butyl-6-iod-2-isopropoxy-benzopyran-4-on.Preferred combinations of active compounds R are those in which the iodochromone (group 23) is selected from the following list: (23-1) 2-butoxy-6-iodo-3-propyl-benzo-pyran-4-one, (23-2) 2-ethoxy-6 -iod-3-propyl-benzopyran-4-one, (23-3) 6-iodo-2-propoxy-3-propyl-benzopyran-4-one, (23-4) 2-but-2-ynyloxy-6 iodo-3-propyl-benzo-pyran-4-one, (23-5) 6-iodo-2- (1-methyl-butoxy) -3-propyl-benzopyran-4-one, (23-6) 2-But 3-enyloxy-6-iodobenzopyran-4-one, (23-7) 3-butyl-6-iodo-2-isopropoxy-benzopyran-4-one.
Besonders bevorzugt sind Wirkstoffkombinationen T, worin das Iodochromon (Gruppe 23) aus der folgenden Liste ausgewählt ist: (23-1) 2-Butoxy-6-iod-3-propyl-benzopyran-4-on, (23-2) 2-Ethoxy-6- iod-3-propyl-benzopyran-4-on.Particular preference is given to active ingredient combinations T in which the iodochromone (group 23) is selected from the following list: (23-1) 2-butoxy-6-iodo-3-propyl-benzopyran-4-one, (23-2) 2- Ethoxy-6-iodo-3-propyl-benzopyran-4-one.
Hervorgehoben sind die in der folgenden Tabelle 18 angeführten Wirkstoffkombinationen R: Tabelle 18: Wirkstoffkombinationen RHighlighted are the active substance combinations R listed in Table 18 below: Table 18: Active substance combinations R
Die erfmdungsgemäßen Wirkstoffkombinationen enthalten neben einem Wirkstoff der Formel (I) mindestens einen Wirkstoff von den Verbindungen der Gruppen (2) bis (23). Sie können darüber hinaus auch weitere fungizid wirksame Zumischkomponenten enthalten. Wenn die Wirkstoffe in den erfindungsgemäßen Wirkstoffkombinationen in bestimmten Gewichtsverhältnissen vorhanden sind, zeigt sich der synergistische Effekt besonders deutlich. Jedoch können die Gewichtsverhältnisse der Wirkstoffe in den Wirkstoffkombinationen in einem relativ großen Bereich variiert werden. Im Allgemeinen enthalten die erfindungsgemäßen Kombinationen Wirkstoffe der Formel (J) und einen Mischpartner aus einer der Gruppen (2) bis (23) in den in der nachfolgenden Tabelle" 19 beispielhaft angegebenen Mischungsverhältnisse.The active compound combinations according to the invention contain, in addition to an active compound of the formula (I), at least one active compound of the compounds of groups (2) to (23). You may also contain other fungicidal Zumischkomponenten. If the active ingredients in the active compound combinations according to the invention are present in certain weight ratios, the synergistic effect is particularly pronounced. However, the weight ratios of the active ingredients in the drug combinations can be varied within a relatively wide range. In general, combinations of active compounds according to the invention of the formula (J) and a mixing partner from one of the groups (2) to (23) mix ratios exemplified in the following in the table. "19
Die Mischungsverhältnisse basieren auf Gewichtsverhältnissen. Das Verhältnis ist zu verstehen als Wirkstoff der Formel (T) : Mischpartner.The mixing ratios are based on weight ratios. The ratio is to be understood as active substance of the formula (T): Mischpartner.
Tabelle 19: MischungsverhältnisseTable 19: Mixing ratios
Das Mischungsverhältnis ist in jedem Fall so zu wählen, dass eine synergistische Mischung erhalten wird. Die Mischungsverhältnisse zwischen der Verbindung der Formel (I) und einer Verbindung aus einer der Gruppen (2) bis (23) kann auch zwischen den einzelnen Verbindungen einer Gruppe variieren. In any case, the mixing ratio should be such that a synergistic mixture is obtained. The mixing ratios between the compound of formula (I) and a compound of any of groups (2) to (23) may also vary between the individual compounds of a group.
Die erfϊndungsgemäßen Wirkstoffkombinationen besitzen sehr gute fungizide Eigenschaften und lassen sich zur Bekämpfung von phytopathogenen Pilzen und Bakterien einsetzen.The active compound combinations according to the invention have very good fungicidal properties and can be used for controlling phytopathogenic fungi and bacteria.
Fungizide lassen sich Pflanzenschutz zur Bekämpfung von Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes und Deuteromycetes einsetzen.Fungicides can be used for the control of Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes.
Bakterizide lassen sich im Pflanzenschutz zur Bekämpfung von Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae und Streptomycetaceae einsetzen.Bactericides can be used in crop protection for controlling Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
Beispielhaft aber nicht begrenzend seien einige Erreger von pilzlichen und bakteriellen Erkrankungen, die unter die oben aufgezählten Oberbegriffe fallen, genannt:By way of example but not limitation, some pathogens of fungal and bacterial diseases, which fall under the above-enumerated generic terms, are named:
Erkrankungen, hervorgerufen durch Erreger des Echten Mehltaus wie z.B.Diseases caused by powdery mildews such as e.g.
Blumeria-Arten, wie beispielsweise Blumeria graminis;Blumeria species, such as Blumeria graminis;
Podosphaera-Arten, wie beispielsweise Podosphaera leucotricha;Podosphaera species, such as Podosphaera leucotricha;
Sphaerotheca-Arten, wie beispielsweise Sphaerotheca füliginea; Uncinula-Arten, wie beispielsweise Uncinula necator;Sphaerotheca species, such as Sphaerotheca fuliginea; Uncinula species, such as Uncinula necator;
Erkrankungen, hervorgerufen durch Erreger von Rostkrankheiten wie z.B. Gymnosporangium-Arten, wie beispielsweise Gymnosporangium sabinae Hemileia-Arten, wie beispielsweise Hemileia vastatrix; Phakopsora-Arten, wie beispielsweise Phakopsora pachyrhizi und Phakopsora meibomiae; Puccinia-Arten, wie beispielsweise Puccinia recondita; Uromyces-Arten, wie beispielsweise Uromyces appendiculatus;Diseases caused by causative agents of rust diseases, such as Gymnosporangium species, such as, for example, Gymnosporangium sabinae Hemileia species, such as, for example, Hemileia vastatrix; Phakopsora species such as Phakopsora pachyrhizi and Phakopsora meibomiae; Puccinia species, such as Puccinia recondita; Uromyces species, such as Uromyces appendiculatus;
Erkrankungen, hervorgerufen durch Erreger der Gruppe der Oomyceten wie z.B. Bremia-Arten, wie beispielsweise Bremia lactucae;Diseases caused by pathogens of the group of Oomycetes, e.g. Bremia species, such as Bremia lactucae;
Peronospora-Arten, wie beispielsweise Peronospora pisi oder P. brassicae;Peronospora species such as Peronospora pisi or P. brassicae;
Phytophthora-Arten, wie beispielsweise Phytophthora infestans;Phytophthora species, such as Phytophthora infestans;
Plasmopara-Arten, wie beispielsweise Plasmopara viticola;Plasmopara species, such as Plasmopara viticola;
Pseudoperonospora-Arten, wie beispielsweise Pseudoperonospora humuli oder Pseudoperonospora cubensis;Pseudoperonospora species, such as, for example, Pseudoperonospora humuli or Pseudoperonospora cubensis;
Pythium-Arten, wie beispielsweise Pythium ultimum; Blattfleckenkrankheiten und Blattwelken, hervorgerufen durch z.B.Pythium species such as Pythium ultimum; Leaf spot diseases and leaf withering, caused by eg
Alternaria-Arten, wie beispielsweise Alternaria solani;Alternaria species, such as Alternaria solani;
Cercospora-Arten, wie beispielsweise Cercospora beticola;Cercospora species, such as Cercospora beticola;
Cladiosporum-Arten, wie beispielsweise Cladiosporium cucumerinum; Cochliobolus-Arten, wie beispielsweise Cochliobolus sativusCladiosporum species, such as Cladiosporium cucumerinum; Cochliobolus species, such as Cochliobolus sativus
(Konidiertform: Drechslera, Syn: Helminthosporium);(Conidic form: Drechslera, Syn: Helminthosporium);
Colletotrichum-Arten, wie beispielsweise Colletotrichum lindemuthanium;Colletotrichum species, such as Colletotrichum lindemuthanium;
Cycloconium-Arten, wie beispielsweise Cycloconium oleaginum;Cycloconium species such as cycloconium oleaginum;
Diaporthe-Arten, wie beispielsweise Diaporthe citri; Elsinoe-Arten, wie beispielsweise Elsinoe fawcettii;Diaporthe species, such as Diaporthe citri; Elsinoe species, such as Elsinoe fawcettii;
Gloeosporium-Arten, wie beispielsweise Gloeosporium laeticolor;Gloeosporium species, such as, for example, Gloeosporium laeticolor;
Glomerella-Arten, wie beispielsweise Glomerella cingulata;Glomerella species, such as Glomerella cingulata;
Guignardia-Arten, wie beispielsweise Guignardia bidwelli;Guignardia species, such as Guignardia bidwelli;
Leptosphaeria-Arten, wie beispielsweise Leptosphaeria maculans; Magnaporthe-Arten, wie beispielsweise Magnaporthe grisea;Leptosphaeria species, such as Leptosphaeria maculans; Magnaporthe species, such as Magnaporthe grisea;
Mycosphaerella-Arten, wie beispielsweise Mycosphaerelle graminicola;Mycosphaerella species, such as Mycosphaerelle graminicola;
Phaeosphaeria-Arten, wie beispielsweise Phaeosphaeria nodorum;Phaeosphaeria species, such as Phaeosphaeria nodorum;
Pyrenophora-Arten, wie beispielsweise Pyrenophora teres;Pyrenophora species, such as, for example, Pyrenophora teres;
Ramularia-Arten, wie beispielsweise Ramularia collo-cygni; Rhynchosporium-Arten, wie beispielsweise Rhynchosporium secalis;Ramularia species, such as Ramularia collo-cygni; Rhynchosporium species, such as Rhynchosporium secalis;
Septoria-Arten, wie beispielsweise Septoria apii;Septoria species, such as Septoria apii;
Typhula-Arten, wie beispielsweise Typhula incarnata;Typhula species, such as Typhula incarnata;
Venturia-Arten, wie beispielsweise Venturia inaequalis;Venturia species, such as Venturia inaequalis;
Wurzel- und Stengelkrankheiten, hervorgerufen durch z.B.Root and stem diseases caused by e.g.
Corticium-Arten, wie beispielsweise Corticium graminearum;Corticium species, such as Corticium graminearum;
Fusarium-Arten, wie beispielsweise Fusarium oxysporum;Fusarium species such as Fusarium oxysporum;
Gaeumannomyces-Arten, wie beispielsweise Gaeumannomyces graminis;Gaeumannomyces species such as Gaeumannomyces graminis;
Rhizoctonia-Arten, wie beispielsweise Rhizoctonia solani; Tapesia-Arten, wie beispielsweise Tapesia acuforrnis;Rhizoctonia species, such as Rhizoctonia solani; Tapesia species, such as Tapesia acuforrnis;
Thielaviopsis-Arten, wie beispielsweise Thielaviopsis basicola;Thielaviopsis species, such as Thielaviopsis basicola;
Ähren- und Rispenerkrankungen (inklusive Maiskolben), hervorgerufen durch z.B. Alternaria-Arten, wie beispielsweise Alternaria spp.; Aspergillus-Arten, wie beispielsweise Aspergillus flavus;Ear and panicle diseases (including corncob) caused by e.g. Alternaria species, such as Alternaria spp .; Aspergillus species, such as Aspergillus flavus;
Cladosporium-Arten, wie beispielsweise Cladosporium spp.; Claviceps-Arten, wie beispielsweise Claviceps purpurea; Fusarium-Arten, wie beispielsweise Fusarium culmorum; Gibberella-Arten, wie beispielsweise Gibberella zeae; Monographella-Arten, wie beispielsweise Monographella nivalis;Cladosporium species such as Cladosporium spp .; Claviceps species, such as Claviceps purpurea; Fusarium species such as Fusarium culmorum; Gibberella species, such as Gibberella zeae; Monographella species, such as Monographella nivalis;
Erkrankungen, hervorgerufen durch Brandpilze wie z.B. Sphacelotheca-Arten, wie beispielsweise Sphacelotheca reiliana; Tilletia-Arten, wie beispielsweise Tilletia caries; Urocystis-Arten, wie beispielsweise Urocystis occulta; Ustilago-Arten, wie beispielsweise Ustilago nuda;Diseases caused by fire fungi, e.g. Sphacelotheca species, such as Sphacelotheca reiliana; Tilletia species, such as Tilletia caries; Urocystis species, such as Urocystis occulta; Ustilago species such as Ustilago nuda;
Fruchtfaule hervorgerufen durch z.B. Aspergillus-Arten, wie beispielsweise Aspergillus flavus; Botrytis-Arten, wie beispielsweise Botrytis cinerea; Penicillium- Arten, wie beispielsweise Penicillium expansum; Sclerotinia-Arten, wie beispielsweise Sclerotinia sclerotiorum; Verticilium-Arten, wie beispielsweise Verticilium alboatrum;Fruit rot caused by e.g. Aspergillus species, such as Aspergillus flavus; Botrytis species, such as Botrytis cinerea; Penicillium species such as Penicillium expansum; Sclerotinia species, such as Sclerotinia sclerotiorum; Verticilium species such as Verticilium alboatrum;
Samen- und bodenbürtige Fäulen und Welken, sowie Sämlingserkrankungen, hervorgerufen durch z.B. Fusarium-Arten, wie beispielsweise Fusarium culmorum;Seed and soil rots and wilts, as well as seedling diseases caused by e.g. Fusarium species such as Fusarium culmorum;
Phytophthora Arten, wie beispielsweise Phytophthora cactorum;Phytophthora species, such as Phytophthora cactorum;
Pythium-Arten, wie beispielsweise Pythium ultimum;Pythium species such as Pythium ultimum;
Rhizoctonia-Arten, wie beispielsweise Rhizoctonia solani;Rhizoctonia species, such as Rhizoctonia solani;
Sclerotium-Arten, wie beispielsweise Sclerotium rolfsii;Sclerotium species, such as Sclerotium rolfsii;
Krebserkrankungen, Gallen und Hexenbesen, hervorgerufen durch z.B.Cancers, galls and witches brooms caused by e.g.
Nectria-Arten, wie beispielsweise Nectria galligena;Nectria species, such as Nectria galligena;
"Welkeerkrankungen hervorgerufen durch z.B. Monilinia-Arten, wie beispielsweise Monilinia laxa; " Wilting diseases caused by eg Monilinia species, such as Monilinia laxa;
Deformationen von Blättern, Blüten und Früchten, hervorgerufen durch z.B. Taphrina-Arten, wie beispielsweise Taphrina deformans;Deformations of leaves, flowers and fruits caused by e.g. Taphrina species, such as Taphrina deformans;
Degenerationserkrankungen holziger pflanzen, hervorgerufen durch z.B. Esca-Arten, wie beispielsweise Phaemoniella clamydospora; Blüten- und Samenerkrankungen, hervorgerufen durch z.B. Botrytis-Arten, wie beispielsweise Botrytis cinerea;Degenerative diseases of woody plants, caused by eg Esca species, such as Phaemoniella clamydospora; Floral and seed diseases caused by, for example, Botrytis species such as Botrytis cinerea;
Erkrankungen von Pflanzenknollen, hervorgerufen durch z.B. Rhizoctonia-Arten, wie beispielsweise Rhizoctonia solani;Diseases of plant tubers caused by e.g. Rhizoctonia species, such as Rhizoctonia solani;
Erkrankungen, hervorgerufen durch bakterielle Erreger wie z.B. Xanthomonas-Arten, wie beispielsweise Xanthomonas campestris pv. oryzae; Pseudomonas-Arten, wie beispielsweise Pseudomonas syringae pv. lachiymans; Erwinia-Arten, wie beispielsweise Erwinia amylovora;Diseases caused by bacterial agents such as e.g. Xanthomonas species, such as Xanthomonas campestris pv. Oryzae; Pseudomonas species, such as Pseudomonas syringae pv. Lachiymans; Erwinia species, such as Erwinia amylovora;
Bevorzugt können die folgenden Krankheiten von Soja-Bohnen bekämpft werden:Preferably, the following diseases of soybean beans can be controlled:
Pilzkrankheiten an Blättern, Stängeln, Schoten und Samen verursacht durch z.B.Fungal diseases on leaves, stems, pods and seeds caused by e.g.
Alternaria leaf spot (Alternaria spec. atrans tenuissima), Anthracnose (Colletotrichum gloeosporoides dematium var. truncatum), Brown spot (Septoria glycines), Cercospora leaf spot and blight (Cercospora Mkuchii), Choanephora leaf blight (Choanephora infundibulifera trispora (Syn.)), Dactuliophora leaf spot (Dactuliophora glycines), Downy Mildew (Peronospora manshurica), Drechslera blight (Drechslera glycini), Frogeye Leaf spot (Cercospora sojina), Leptosphaerulina Leaf Spot (Leptosphaerulina trifolii), Phyllostica Leaf Spot (Phyllosticta sojaecola), Powdery Mildew (Microsphaera diffusa), Pyrenochaeta Leaf Spot (Pyrenochaeta glycines), Rhizoctonia Aerial, Foliage, and Web Blight (Rhizoctonia solani), Rust (Phakopsora pachyrhizi), Scab (Sphaceloma glycines), Stemphylium Leaf Blight (Stemphylium botryosum), Target Spot (Corynespora cassiicola)Anthracnose (Colletotrichum gloeosporoides dematium var. Truncatum), Brown spot (Septoria glycines), Cercospora leaf spot and blight (Cercospora mkuchii), Choanephora leaf blight (Choanephora infundibulifera trispora (Syn.)), Alternaria leaf spot (Alternaria spec. Atrans tenuissima) , Dactuliophora leaf spot (Dactuliophora glycines), Downy Mildew (Peronospora manshurica), Drechslera blight (Drechslera glycini), Frogeye leaf spot (Cercospora sojina), Leptosphaerulina leaf spot (Leptosphaerulina trifolii), Phyllostica leaf spot (Phyllosticta sojaecola), Powdery Mildew (Phyllosticta sojaecola) Microsphaera diffusa), Pyrenochaeta Leaf Spot (Pyrenochaeta glycines), Rhizoctonia Aerial, Foliage and Web Blight (Rhizoctonia solani), Rust (Phakopsora pachyrhizi), Scab (Sphaceloma glycines), Stemphylium Leaf Blight (Stemphylium botryosum), Target Spot (Corynespora cassiicola )
Pilzkrankheiten an Wurzeln und der Stängelbasis verursacht durch z.B. Black Root Rot (Calonectria crotalariae), Charcoal Rot (Macrophomina phaseolina), Fusarium Blight or WiIt, Root Rot, and Pod and Collar Rot (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium equiseti), Mycoleptodiscus Root Rot (Mycoleptodiscus terrestris), Neocosmo- spora (Neocosmopspora vasinfecta), Pod and Stem Blight (Diaporthe phaseolorum), Stern Canker (Diaporthe phaseolorum var. caulivora), Phytophthora Rot (Phytophthora megasperma), Brown Stem Rot (Phialophora gregata), Pythium Rot (Pythium aphanidermatum, Pythium irreguläre, Pythium debaryanum, Pythium myriotylum, Pythium ultimum), Rhizoctonia Root Rot, Stem Decay, and Damping-Off (Rhizoctonia solani), Sclerotinia Stem Decay (Sclerotinia sclerotiorum), Sclerotinia Southern Blight (Sclerotinia rolfsii), Thielaviopsis Root Rot (Thielaviopsis basicola).Fungal diseases on roots and stem base caused by e.g. Black Root Red (Calonectria crotalariae), Charcoal Red (Macrophomina phaseolina), Fusarium Blight or Wiit, Root Red, and Pod and Collar Red (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium equiseti), Mycoleptodiscus Root Red (Mycoleptodiscus terrestris), Neocosmospora (Neocosmopspora vasinfecta), Pod and Stem Blight (Diaporthe phaseolorum), Star Canker (Diaporthe phaseolorum var. Caulivora), Phytophthora red (Phytophthora megasperma), Brown Stem Red (Phialophora gregata), Pythium Red (Pythium aphanidermatum, Pythium irregular , Pythium debaryanum, Pythium myriotylum, Pythium ultimum), Rhizoctonia Root Red, Stem Decay, and Damping Off (Rhizoctonia solani), Sclerotinia Stem Decay (Sclerotinia sclerotiorum), Sclerotinia Southern Blight (Sclerotinia rolfsii), Thielaviopsis Root Red (Thielaviopsis basicola) ,
Die gute Pflanzenverträglichkeit der Wirkstoffkombinationen in den zur Bekämpfung von Pflanzenkrankheiten notwendigen Konzentrationen erlaubt eine Behandlung von ganzen Pflanzen (oberir- dische Pflanzenteile und Wurzeln), von Pflanz- und Saatgut, und des Bodens. Die erfindungsgemäßen Wirlcstoffkombinationen können zur Blaτtapplikation oder auch als Beizmittel eingesetzt werden.The good plant tolerance of the active substance combinations in the concentrations necessary for the control of plant diseases makes it possible to treat whole plants (upper plants). plant parts and roots), of plant and seed, and of the soil. The active substance combinations according to the invention can be used for blush application or else as mordant.
Die gute Pflanzenverträglichkeit der verwendbaren Wirkstoffe in den zur Bekämptung von Pflan- zenkrankheiten notwendigen Konzentrationen erlaubt eine Behandlung des Saatguts. Die erfindungsgemäßen Wirkstoffe können somit als Beizmittel eingesetzt werden.The good plant tolerance of the usable active ingredients in the concentrations necessary for the control of plant diseases allows a treatment of the seed. The active compounds according to the invention can thus be used as mordants.
Ein großer Teil des durch phytopathogene Pilze verursachten Schadens an Kulturpflanzen entsteht bereits durch den Befall des Saatguts während der Lagerung und nach dem Einbringen des Saatguts in den Boden sowie während und unmittelbar nach der Keimung der Pflanzen. Diese Phase ist besonders kritisch, da die Wurzeln und Sprosse der wachsenden Pflanze besonders empfindlich sind und bereits ein geringer Schaden zum Absterben der ganzen Pflanze fuhren kann. Es besteht daher ein insbesondere großes Interesse daran, das Saatgut und die keimende Pflanze durch den Einsatz geeigneter Mittel zu schützen.Much of the damage to crops caused by phytopathogenic fungi is already produced by infestation of the seed during storage and after introduction of the seed into the soil and during and immediately after germination of the plants. This phase is particularly critical, as the roots and shoots of the growing plant are particularly sensitive and already a small damage can lead to the death of the entire plant. There is therefore a particular interest in protecting the seed and the germinating plant by the use of suitable agents.
Die Bekämpfung von phytopathogenen Pilzen, die Pflanzen nach dem Auflaufen schädigen, erfolgt in erster Linie durch die Behandlung des Bodens und der oberirdischen Pflanzenteile mit Pflanzenschutzmitteln. Aufgrund der Bedenken hinsichtlich eines möglichen Einflusses der Pflanzenschutzmittel auf die Umwelt und die Gesundheit von Menschen und Tieren gibt es Anstrengungen, die Menge der ausgebrachten Wirkstoffe zu vermindern.The control of phytopathogenic fungi, which damage plants after emergence, takes place primarily through the treatment of the soil and the above-ground parts of plants with pesticides. Due to concerns about the potential impact of crop protection products on the environment and human and animal health, efforts are being made to reduce the amount of active ingredients applied.
Die Bekämpfung von phytopathogenen Pilzen durch die Behandlung des Saatguts von Pflanzen ist seit langem bekannt und ist Gegenstand ständiger Verbesserungen. Dennoch ergeben sich bei der Behandlung von Saatgut eine Reihe von Problemen, die nicht immer zufrieden stellend gelöst werden können. So ist es erstrebenswert, Verfahren zum Schutz des Saatguts und der keimenden Pflanze zu entwickeln, die das zusätzliche Ausbringen von Pflanzenschutzmitteln nach der Saat oder nach dem Auflaufen der Pflanzen überflüssig machen oder zumindest deutlich verringern. Es ist weiterhin erstrebenswert, die Menge des eingesetzten Wirkstoffs dahingehend zu optimieren, dass das Saatgut und die keimende Pflanze vor dem Befall durch phytopathogene Pilze bestmöglich geschützt wird, ohne jedoch die Pflanze selbst durch den eingesetzten Wirkstoff zu schädigen. Insbesondere sollten Verfahren zur Behandlung von Saatgut auch die intrinsischen fungiziden Eigenschaften transgener Pflanzen einbeziehen, um einen optimalen Schutz des Saatguts und der keimenden Pflanze bei einem minimalen Aufwand an Pflanzenschutzmitteln zu erreichen. Die vorliegende Erfindung bezieht sich daher insbesondere auch auf ein Verfahren zum Schutz von Saatgut und keimenden Pflanzen vor dem Befall von phytopathogenen Pilzen, indem das Saatgut mit einem erfϊndungsgemäßen Mittel behandelt wird.The control of phytopathogenic fungi by the treatment of the seed of plants has long been known and is the subject of constant improvement. Nevertheless, there are a number of problems in the treatment of seeds that can not always be satisfactorily resolved. Thus, it is desirable to develop methods for protecting the seed and the germinating plant, which eliminate or at least significantly reduce the additional application of crop protection agents after sowing or after emergence of the plants. It is also desirable to optimize the amount of the active ingredient used in such a way that the seed and the germinating plant is best protected against attack by phytopathogenic fungi, but without damaging the plant itself by the active ingredient used. In particular, methods for treating seed should also include the intrinsic fungicidal properties of transgenic plants in order to achieve optimum protection of the seed and the germinating plant with a minimum of pesticide use. The present invention therefore more particularly relates to a method of protecting seeds and germinating plants from the infestation of phytopathogenic fungi by treating the seed with an agent according to the invention.
Die Erfindung bezieht sich ebenfalls auf die Verwendung der erfindungsgemäßen Mittel zur Behandlung von Saatgut zum Schutz des Saatguts und der keimenden Pflanze vor phytopathogenen Pilzen.The invention also relates to the use of the seed treatment agents of the invention for protecting the seed and the germinating plant from phytopathogenic fungi.
Weiterhin bezieht sich die Erfindung auf Saatgut, welches zum Schutz vor phytopathogenen Pilzen mit einem erfindungsgemäßen Mittel behandelt wurde.Furthermore, the invention relates to seed which has been treated with an agent according to the invention for protection against phytopathogenic fungi.
Einer der Vorteile der vorliegenden Erfindung ist es, dass aufgrund der besonderen systemischen Eigenschaften der erfϊndungsgemäßen Mittel die Behandlung des Saatguts mit diesen Mitteln nicht nur das Saatgut selbst, sondern auch die daraus hervorgehenden Pflanzen nach dem Auflaufen vor phytopathogenen Pilzen schützt. Auf diese Weise kann die unmittelbare Behandlung der Kultur zum Zeitpunkt der Aussaat oder kurz danach entfallen.One of the advantages of the present invention is that because of the particular systemic properties of the compositions of the invention, treatment of the seed with these agents not only protects the seed itself but also the resulting plants after emergence from phytopathogenic fungi. In this way, the immediate treatment of the culture at the time of sowing or shortly afterwards can be omitted.
Ebenso ist es als vorteilhaft anzusehen, dass die erfindungsgemäßen Mischungen insbesondere auch bei transgenem Saatgut eingesetzt werden können.It is likewise to be regarded as advantageous that the mixtures according to the invention can also be used in particular in the case of transgenic seed.
Die erfindungsgemäßen Mittel eignen sich zum Schutz von Saatgut jeglicher Pflanzensorte, die in der Landwirtschaft, im Gewächshaus, in Forsten oder im Gartenbau eingesetzt wird. Insbesondere handelt es sich dabei um Saatgut von Getreide (wie Weizen, Gerste, Roggen, Hirse und Hafer), Mais, Baumwolle, Soja, Reis, Kartoffeln, Sonnenblume, Bohne, Kaffee, Rübe (z.B. Zuckerrübe und Futterrübe), Erdnuss, Gemüse (wie Tomate, Gurke, Zwiebeln und Salat), Rasen und Zierpflanzen. Be- sondere Bedeutung kommt der Behandlung des Saatguts von Getreide (wie Weizen, Gerste, Roggen und Hafer), Mais und Reis zu.The compositions according to the invention are suitable for the protection of seeds of any plant variety used in agriculture, in the greenhouse, in forests or in horticulture. In particular, these are seeds of cereals (such as wheat, barley, rye, millet and oats), corn, cotton, soy, rice, potatoes, sunflower, bean, coffee, turnip (eg sugarbeet and fodder), peanut, vegetables ( like tomato, cucumber, onions and lettuce), lawn and ornamental plants. Of particular importance is the treatment of the seeds of cereals (such as wheat, barley, rye and oats), maize and rice.
Im Rahmen der vorliegenden Erfindung wird das erfindungsgemäßes Mittel alleine oder in einer geeigneten Formulierung auf das Saatgut aufgebracht. Vorzugsweise wird das Saatgut in einem Zustand behandelt, in dem so stabil ist, dass keine Schäden bei der Behandlung auftreten. Im Allgemeinen kann die Behandlung des Saatguts zu jedem Zeitpunkt zwischen der Ernte und der Aussaat erfolgen. Üblicherweise wird Saatgut verwendet, das von der Pflanze getrennt und von Kolben, Schalen, Stängeln, Hülle, Wolle oder Fruchtfleisch befreit wurde. So kann zum Beispiel Saatgut verwendet werden, das geerntet, gereinigt und bis zu einem Feuchtigkeitsgehalt von unter 15 Gew.-% getrocknet wurde. Alternativ kann auch Saatgut verwendet werden, das nach dem Trocknen z.B. mit Wasser behandelt und dann erneut getrocknet wurde. Im Allgemeinen muss bei der Behandlung des Saatguts darauf geachtet werden, dass die Menge des auf das Saatgut aufgebrachten erfindungsgemäßen Mittels und/oder weiterer Zusatzstoffe so gewählt wird, dass die Keimung des Saatguts nicht beeinträchtigt bzw. die daraus hervorgehende Pflanze nicht geschädigt wird. Dies ist vor allem bei Wirkstoffen zu beachten, die in bestimmten Aufwand- mengen phytotoxische Effekte zeigen können.In the context of the present invention, the agent according to the invention is applied to the seed alone or in a suitable formulation. Preferably, the seed is treated in a condition that is so stable that no damage occurs during the treatment. In general, the treatment of the seed can be done at any time between harvesting and sowing. Usually, seed is used which has been separated from the plant and freed from flasks, shells, stems, hull, wool or pulp. For example, seed may be used which has been harvested, cleaned and dried to a moisture content below 15% by weight. Alternatively, seed can also be used, which after drying, for example, treated with water and then dried again. In general, care must be taken in the treatment of the seed that the amount of the agent and / or other additives applied to the seed is chosen so that germination of the seed is not impaired or the resulting plant is not damaged. This should be taken into account, in particular, for active substances which may show phytotoxic effects in certain quantities.
Die erfmdungsgemäßen Mittel können unmittelbar aufgebracht werden, also ohne weitere Komponenten zu enthalten und ohne verdünnt worden zu sein. In der Regel ist es vorzuziehen, die Mittel in Form einer geeigneten Formulierung auf das Saatgut aufzubringen. Geeignete Formulierungen und Verfahren für die Saatgutbehandlung sind dem Fachmann bekannt und werden z.B. in den folgenden Dokumenten beschrieben: US 4,272,417 A, US 4,245,432 A, US 4,808,430 A, US 5,876,739 A, US 2003/0176428 Al, WO 2002/080675 Al, WO 2002/028186 A2.The agents according to the invention can be applied directly, ie without containing further components and without being diluted. In general, it is preferable to apply the agents to the seed in the form of a suitable formulation. Suitable formulations and methods for seed treatment are known to those skilled in the art and are described e.g. in the following documents: US 4,272,417 A, US 4,245,432 A, US 4,808,430 A, US 5,876,739 A, US 2003/0176428 A1, WO 2002/080675 A1, WO 2002/028186 A2.
Die erfindungsgemäßen Wirkstoffkombinationen eignen sich auch zur Steigerung des Ernteertrages. Sie sind außerdem mindertoxisch und weisen eine gute Pflanzenverträglichkeit auf.The active compound combinations according to the invention are also suitable for increasing crop yield. They are also low toxicity and have good plant tolerance.
Erfindungsgemäß können alle Pflanzen und Pflanzenteile behandelt werden. Unter Pflanzen werden hierbei alle Pflanzen und Pflanzenpopulationen verstanden, wie erwünschte und unerwünschte Wildpflanzen oder Kulturpflanzen (einschließlich natürlich vorkommender Kulturpflanzen). Kulturpflan- zen können Pflanzen sein, die durch konventionelle Züchtungs- und Optimierungsmethoden oder durch biotechnologische und gentechnologische Methoden oder Kombinationen dieser Methoden erhalten werden können, einschließlich der transgenen Pflanzen und einschließlich der durch Sorten- schutzrechte schützbaren oder nicht schützbaren Pflanzensorten. Unter Pflanzenteilen sollen alle oberirdischen und unterirdischen Teile und Organe der Pflanzen, wie Spross, Blatt, Blüte und Wurzel verstanden werden, wobei beispielhaft Blätter, Nadeln, Stängel, Stämme, Blüten, Fruchtkörper, Früchte und Samen sowie Wurzeln, Knollen und Rhizome aufgeführt werden. Zu den Pflanzenteilen gehört auch Erntegut sowie vegetatives und generatives Vermehrungsmaterial, beispielsweise Stecklinge, Knollen, Rhizome, Ableger und Samen.According to the invention, all plants and parts of plants can be treated. In this context, plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants). Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant variety rights. Plant parts are to be understood as meaning all aboveground and subterranean parts and organs of the plants, such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes. The plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
Die erfindungsgemäße Behandlung der Pflanzen und Pflanzenteile mit den Wirkstoffen erfolgt direkt oder durch Einwirkung auf deren Umgebung, Lebensraum oder Lagerraum nach den üblichen Behandlungsmethoden, z.B. durch Tauchen, Sprühen, Verdampfen, Vernebeln, Streuen, Aufstreichen und bei Vermehrungsmaterial, insbesondere bei Samen, weiterhin durch ein- oder mehrschichtiges Umhüllen.The treatment according to the invention of the plants and plant parts with the active ingredients is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, spreading, spreading and in propagation material, in particular in seeds, further by single or multi-layer wrapping.
Wie bereits oben erwähnt, können erfindungsgemäß alle Pflanzen und deren Teile behandelt werden. In einer bevorzugten Ausföhrungsform werden wild vorkommende oder durch konventionelle biolo- gische Zuchtmethoden, wie Kreuzung oder Protoplastenfusion erhaltenen Pflanzenarten und Pflanzensorten sowie deren Teile behandelt. Ih einer weiteren bevorzugten Ausfuhrungsform werden transgene Pflanzen und Pflanzensorten, die durch gentechnologische Methoden gegebenenfalls in Kombination mit konventionellen Methoden erhalten wurden (Genetically Modified Organisms) und deren Teile behandelt. Der Begriff „Teile" bzw. „Teile von Pflanzen" oder „Pflanzenteile" wurde oben erläutert.As already mentioned above, according to the invention all plants and their parts can be treated. In a preferred embodiment, wild or conventional biologic treated genetic breeding methods, such as hybridization or protoplast fusion obtained plant species and plant varieties and their parts. In a further preferred embodiment, transgenic plants and plant cultivars obtained by genetic engineering, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated. The term "parts" or "parts of plants" or "plant parts" has been explained above.
Besonders bevorzugt werden erfindungsgemäß Pflanzen der jeweils handelsüblichen oder in Gebrauch befindlichen Pflanzensorten behandelt.It is particularly preferred according to the invention to treat plants of the respective commercially available or in use plant cultivars.
Je nach Pflanzenarten bzw. Pflanzensorten, deren Standort und Wachstumsbedingungen (Böden, Klima, Vegetationsperiode, Ernährung) können durch die erfindungsgemäße Behandlung auch überadditive („synergistische") Effekte auftreten. So sind beispielsweise erniedrigte Aufwandmengen und/oder Erweiterungen des Wirkungsspektrums und/oder eine Verstärkung der Wirkung der erfin- dungsgemäß verwendbaren Stoffe und Mittel, besseres Pflanzenwachstum, erhöhte Toleranz gegenüber hohen oder niedrigen Temperaturen, erhöhte Toleranz gegen Trockenheit oder gegen Wasserbzw. Bodensalzgehalt, erhöhte Blühleistung, erleichterte Ernte, Beschleunigung der Reife, höhere Ernteerträge, höhere Qualität und/oder höherer Ernährungswert der Ernteprodukte, höhere Lagerfähigkeit und/oder Bearbeitbarkeit der Ernteprodukte möglich, die über die eigentlich zu erwartenden Effekte hinausgehen.Depending on the plant species or plant cultivars, their location and growth conditions (soils, climate, vegetation period, nutrition), the treatment according to the invention may also give rise to superadditive ("synergistic") effects, for example reduced application rates and / or extensions of the activity spectrum and / or a Enhancement of the effect of the substances and agents usable according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to water or soil salt content, increased flowering efficiency, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or workability of the harvested products possible, which go beyond the actual expected effects.
Zu den bevorzugten erfindungsgemäß zu behandelnden transgenen (gentechnologisch erhaltenen) Pflanzen bzw. Pflanzensorten gehören alle Pflanzen, die durch die gentechnologische Modifikation genetisches Material erhielten, welches diesen Pflanzen besondere vorteilhafte wertvolle Eigen- schatten („Traits") verleiht. Beispiele für solche Eigenschaften sind besseres Pflanzenwachstum, erhöhte Toleranz gegenüber hohen oder niedrigen Temperaturen, erhöhte Toleranz gegen Trockenheit oder gegen Wasser- bzw. Bodensalzgehalt, erhöhte Blühleistung, erleichterte Ernte, Beschleunigung der Reife, höhere Ernteerträge, höhere Qualität und/oder höherer Ernährungswert der Ernteprodukte, höhere Lagerfähigkeit und/oder Bearbeitbarkeit der Ernteprodukte. Weitere und besonders hervorgehobene Beispiele für solche Eigenschaften sind eine erhöhte Abwehr der Pflanzen gegen tierische und mikrobielle Schädlinge, wie gegenüber Insekten, Milben, pflanzenpathogenen Pilzen, Bakterien und/oder Viren sowie eine erhöhte Toleranz der Pflanzen gegen bestimmte herbizide Wirkstoffe. Als Beispiele transgener Pflanzen werden die wichtigen Kulturpflanzen, wie Getreide (Weizen, Reis), Mais, Soja, Kartoffel, Baumwolle, Raps sowie Obstpflanzen (mit den Früchten Äpfel, Birnen, Zitrusfrüchten und Weintrauben) erwähnt, wobei Mais, Soja, Kartoffel, Baumwolle und Raps besonders hervorgehoben werden. Als Eigenschaften („Traits") werden besonders hervor- gehoben die erhöhte Abwehr der Pflanzen gegen Insekten durch in den Pflanzen entstehende Toxine, insbesondere solche, die durch das genetische Material aus Bacillus thuringiensis (z.B. durch die Gene CryΙA(a), CryIA(b), CryIA(c), CryJIA, CrylllA, CrylHB2, Cry9c Cry2Ab, Cry3Bb und CrylF sowie deren Kombinationen) in den Pflanzen erzeugt werden (im folgenden „Bt Pflanzen"). Als Eigenschaften („Traits") werden weiterhin besonders hervorgehoben die erhöhte Toleranz der Pflanzen gegenüber bestimmten herbiziden Wirkstoffen, beispielsweise Imidazolinonen, Sulfonylharnstoffen, Glyphosate oder Phosphinotricin (z.B. ,,PAT"-Gen). Die jeweils die gewünschten Eigenschaften („Traits") verleihenden Gene können auch in Kombinationen miteinander in den transgenen Pflanzen vorkommen. Als Beispiele für „Bt Pflanzen" seien Maissorten, Baumwollsorten, Sojasorten und Kartoffelsorten genannt, die unter den Handelsbezeichnungen YEELD GARD® (z.B. Mais, Baumwolle, Soja), KnockOut® (z.B. Mais), StarLink® (z.B. Mais), Bollgard® (Baumwolle), Nucotn® (Baumwolle) und NewLeaf® (Kartoffel) vertrieben werden. Als Beispiele für Herbizid tolerante Pflanzen seien Maissorten, Baumwollsorten und Sojasorten genannt, die unter den Handelsbezeichnungen Roundup Ready® (Toleranz gegen Glyphosate z.B. Mais, Baumwolle, Soja), Liberty Link® (Toleranz gegen Phosphinotricin, z.B. Raps), IMI® (Toleranz gegen Imidazolmone) und STS® (Toleranz gegen Sulfonylharnstoffe z.B. Mais) vertrieben werden. Als Herbizid resistente (konventionell auf Herbizid-Toleranz gezüchtete) Pflanzen seien auch die unter der Bezeichnung Clearfϊeld® vertriebenen Sorten (z.B. Mais) erwähnt. Selbstverständlich gelten diese Aussagen auch für in der Zukunft entwickelte bzw. zukünftig auf den Markt kommende Pflanzensorten mit diesen oder zukünftig entwickelten genetischen Eigenschaften („Traits").The preferred plants or plant cultivars to be treated according to the invention include all plants which have obtained genetic material by the genetic modification which gives these plants particularly advantageous valuable properties ("traits".) Examples of such properties are better Plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or soil salt content, increased flowering efficiency, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or Further and particularly emphasized examples of such properties are an increased defense of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and / or Vir and increased tolerance of the plants to certain herbicidal active substances. Examples of transgenic plants include the important crops such as cereals (wheat, rice), corn, soy, potato, cotton, rapeseed and fruit plants (with the fruits apples, pears, citrus fruits and grapes), with corn, soy, potato, cotton and rapeseed should be highlighted. Traits are particularly raised the increased defense of the plants against insects by toxins formed in the plants, in particular those by the genetic material from Bacillus thuringiensis (eg by the genes CryΙA (a), CryIA (b), CryIA (c), CryJIA, CrylllA, CrylHB2, Cry9c Cry2Ab, Cry3Bb and CrylF and their combinations) in the plants (hereinafter "Bt plants") .The traits which are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones. Sulfonylureas, glyphosate or phosphinotricin (eg "PAT" gene) The genes which confer the desired properties ("traits") can also be present in combinations with one another in the transgenic plants. Examples of "Bt plants" are maize varieties, cotton varieties, soya bean varieties and potato varieties may be mentioned that under the trade names yeeld GARD ® (for example maize, cotton, soya beans), KnockOut ® (for example maize), StarLink ® (for example maize), Bollgard ® ( cotton), Nucotn® (cotton) and NewLeaf ® (potato). Examples of herbicide-tolerant plants are maize varieties, cotton varieties and soybean varieties may be mentioned that, under the trade names Roundup Ready ® (tolerance to glyphosate, for example maize, cotton, soybeans) Liberty Link® (tolerance to phosphinotricin, eg rapeseed), IMI® (tolerance to imidazolmone) and STS® (tolerance to sulfonylureas eg maize) are also marketed as herbicide-resistant (conventionally grown on herbicide tolerance) plants Clearfϊeld ® mentioned varieties (eg maize) Of course, these statements also apply to future developed or future on the market Pfl cultivars with these or future developed genetic traits.
Die erfindungsgemäßen Wirkstoffkombinationen können in Abhängigkeit von ihren jeweiligen physikalischen und/oder chemischen Eigenschaften in die üblichen Formulierungen überführt werden, wie Lösungen, Emulsionen, Suspensionen, Pulver, Stäubemittel, Schäume, Pasten, lösliche Pulver, Granulate, Aerosole, Suspensions-Emulsions-Konzentrate, Wirkstoff-imprägnierte Natur- und synthetische Stoffe sowie Feinstverkapselungen in polymeren Stoffen und in Hüllmassen für Saatgut, sowie ULV-KaIt- und Warmnebel-Formulierungen.The active compound combinations according to the invention can be converted into the customary formulations depending on their respective physical and / or chemical properties, such as solutions, emulsions, suspensions, powders, dusts, foams, pastes, soluble powders, granules, aerosols, suspension-emulsion concentrates, Active substance-impregnated natural and synthetic substances as well as ultra-fine encapsulations in polymeric substances and in coating compositions for seeds, as well as ULV-KaIt and warm mist formulations.
Diese Formulierungen werden in bekannter Weise hergestellt, z.B. durch Vermischen der Wirkstoffe bzw. der Wirkstoffkombinationen mit Streckmitteln, also flüssigen Lösungsmitteln, unter Druck stehenden verflüssigten Gasen und/oder festen Trägerstoffen, gegebenenfalls unter Verwendung von oberflächenaktiven Mitteln, also Emulgiermitteln und/oder Dispergiermitteln und/oder schaumerzeugenden Mitteln.These formulations are prepared in a known manner, e.g. by mixing the active compounds or the active compound combinations with extenders, ie liquid solvents, liquefied gases under pressure and / or solid carriers, optionally with the use of surface-active agents, ie emulsifiers and / or dispersants and / or foam-forming agents.
Im Falle der Benutzung von Wasser als Streckmittel können z.B. auch organische Lösungsmittel als Hilfslösungsmittel verwendet werden. Als flüssige Lösungsmittel kommen im Wesentlichen infrage: Aromaten, wie Xylol, Toluol oder Alkylnaphthaline, chlorierte Aromaten oder chlorierte aliphatische Kohlenwasserstoffe, wie Chlorbenzole, Chlorethylene oder Methylenchlorid, aliphatische Kohlenwasserstoffe, wie Cyclohexan oder Paraffine, z.B. Erdölfraktionen, mineralische und pflanzliche Öle, Alkohole, wie Butanol oder Glycol sowie deren Ether und Ester, Ketone, wie Aceton, Methyl- ethylketon, Methylisobutylketon oder Cyclohexanon, stark polare Lösungsmittel wie Dimethyl- formamid und Dimethylsulfoxid, sowie Wasser.In the case of using water as extender, for example, organic solvents can also be used as auxiliary solvents. As liquid solvents are essentially in question: Aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols, such as butanol or glycol, and their ethers and esters , Ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
Mit verflüssigten gasförmigen Streckmitteln oder Trägerstoffen sind solche Flüssigkeiten gemeint, welche bei normaler Temperatur und unter Normaldruck gasförmig sind, z.B. Aerosol-Treibgase, wie Butan, Propan, Stickstoff und Kohlendioxid.By liquefied gaseous diluents or carriers are meant those liquids which are gaseous at normal temperature and under normal pressure, e.g. Aerosol propellants, such as butane, propane, nitrogen and carbon dioxide.
Als feste Trägerstoffe kommen infrage: z.B. Ammoniumsalze und natürliche Gesteinsmehle, wie Kaoline, Tonerden, Talkum, Kreide, Quarz, Attapulgit, Montmorillonit oder Diatomeenerde und synthetische Gesteinsmehle, wie hochdisperse Kieselsäure, Aluminiumoxid und Silikate. Als feste Trä- gerstoffe für Granulate kommen infrage: z.B. gebrochene und fraktionierte natürliche Gesteine wie Calcit, Marmor, Bims, Sepiolith, Dolomit sowie synthetische Granulate aus anorganischen und organischen Mehlen sowie Granulate aus organischem Material wie Sägemehl, Kokosnussschalen, Maiskolben und Tabakstängel. Als Emulgier- und/oder schaumerzeugende Mittel kommen infrage: z.B. nichtionogene und anionische Emulgatoren, wie Polyoxyethylen-Fettsäureester, Polyoxyethylen- Fettalkoholether, z.B. Alkylarylpolyglycolether, Alkylsulfonate, Alkylsulfate, Arylsulfonate sowie Eiweißhydrolysate. Als Dispergiermittel kommen infrage: z.B. Lignin-Sulfitablaugen und Methyl- cellulose.Suitable solid carriers are: e.g. Ammonium salts and ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as fumed silica, alumina and silicates. Suitable solid carriers for granules are: e.g. Cracked and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, coconut shells, corn cobs and tobacco stems. Suitable emulsifying and / or foaming agents are: e.g. nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolysates. Suitable dispersants are: e.g. Lignin sulphite waste liquors and methyl cellulose.
Es können in den Formulierungen Haftmittel wie Carboxymethylcellulose, natürliche und syntheti- sehe pulverige, körnige oder latexförmige Polymere verwendet werden, wie Gummiarabicum, Polyvinylalkohol, Polyvinylacetat, sowie natürliche Phospholipide, wie Kephaline und Lecithine, und synthetische Phospholipide. Weitere Additive können mineralische und vegetabile Öle sein.It can be used in the formulations adhesives such as carboxymethyl cellulose, natural and synthetic see powdery, granular or latex-like polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins, and synthetic phospholipids. Other additives may be mineral and vegetable oils.
Es können Farbstoffe wie anorganische Pigmente, z.B. Eisenoxid, Titanoxid, Ferrocyanblau und organische Farbstoffe, wie Alizarin-, Azo- und Metallphthalocyaninfarbstoffe und Spurennährstoffe, wie Salze von Eisen, Mangan, Bor, Kupfer, Kobalt, Molybdän und Zink verwendet werden. Der Wirkstoffgehalt der aus den handelsüblichen Formulierungen bereiteten Anwendungsformen kann in weiten Bereichen variieren. Die Wirkstoffkonzentration der Anwendungsformen zum Bekämpfen tierischer Schädlingen wie Insekten und Akariden kann von 0,0000001 bis zu 95 Gew.-% Wirkstoff, vorzugsweise zwischen 0,0001 und 1 Gew.-% liegen. Die Anwendung geschieht in einer den Anwendungsformen angepassten üblichen Weise. Die Formulierungen zur Bekämpfung unerwünschter phytopathogener Pilze enthalten im Allgemeinen zwischen 0,1 und 95 Gew.-% Wirkstoffe, vorzugsweise zwischen 0,5 und 90 %.Dyes such as inorganic pigments such as iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used. The active substance content of the application forms prepared from the commercial formulations can vary within wide ranges. The active ingredient concentration of the use forms for controlling animal pests such as insects and acarids may be from 0.0000001 to 95% by weight of active compound, preferably between 0.0001 and 1% by weight. The application is done in a custom forms adapted to the application forms. The formulations for controlling undesired phytopathogenic fungi generally contain between 0.1 and 95% by weight of active ingredients, preferably between 0.5 and 90%.
Die erfϊndungsgemäßen Wirkstoffkombinationen können als solche, in Form ihrer Formulierungen oder den daraus bereiteten Anwendungsformen, wie gebrauchsfertige Lösungen, emulgierbare Konzentrate, Emulsionen, Suspensionen, Spritzpulver, lösliche Pulver, Stäubemittel und Granulate, angewendet werden. Die Anwendung geschieht in üblicher Weise, z.B. durch Gießen (drenchen), Tröpfchenbewässerung, Verspritzen, Versprühen, Verstreuen, Verstäuben, Verschäumen, Bestreiche, Verstreichen, Trockenbeizen, Feuchtbeizen, Nassbeizen, Schlämmbeizen, Inkrustieren usw.The active compound combinations according to the invention can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, emulsifiable concentrates, emulsions, suspensions, wettable powders, soluble powders, dusts and granules. The application is done in the usual way, e.g. by pouring (drenchen), drip irrigation, spraying, spraying, scattering, dusting, foaming, brushing, spreading, dry pickling, wet pickling, wet pickling, slurry pickling, encrusting, etc.
Die erfindungsgemäßen Wirkstoffkombinationen können in handelsüblichen Formulierungen sowie in den aus diesen Formulierungen bereiteten Anwendungsformen in Mischung mit anderen Wirkstoffen, wie Insektiziden, Lockstoffen, Sterilantien, Bakteriziden, Akariziden, Nematiziden, Fungiziden, wachstumsregulierenden Stoffen oder Herbiziden vorliegen.The active compound combinations according to the invention can be present in commercially available formulations as well as in the formulations prepared from these formulations in admixture with other active ingredients, such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances or herbicides.
Beim Einsatz der erfϊndungsgemäßen Wirkstoffkombinationen können die Aufwandmengen je nach Applikationsart innerhalb eines größeren Bereichs variiert werden. Bei der Behandlung von Pflanzenteilen liegen die Aufwandmengen an Wirkstoffkombination im allgemeinen zwischen 0,1 und 10000 g/ha, vorzugsweise zwischen 10 und 1 000 g/ha. Bei der Saatgutbehandlung liegen die Aufwandmengen an Wirkstoffkombination im allgemeinen zwischen 0,001 und 50 g pro Kilogramm Saatgut, vorzugsweise zwischen 0,01 und 10 g pro Kilogramm Saatgut. Bei der Behandlung des Bodens liegen die Aufwandmengen an Wirkstoffkombination im allgemeinen zwischen 0,1 und 10 000 g/ha, vorzugsweise zwischen 1 und 5 000 g/ha.When using the active compound combinations according to the invention, the application rates can be varied within a substantial range, depending on the mode of administration. In the treatment of parts of plants, the application rates of active compound combination are generally between 0.1 and 10,000 g / ha, preferably between 10 and 1,000 g / ha. In the seed treatment, the application rates of active ingredient combination are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 10 g per kilogram of seed. In the treatment of the soil, the application rates of active ingredient combination are generally between 0.1 and 10,000 g / ha, preferably between 1 and 5,000 g / ha.
Die Wirkstoffkombinationen können als solche, in Form von Konzentraten oder allgemein üblichen Formulierungen wie Pulver, Granulate, Lösungen, Suspensionen, Emulsionen oder Pasten angewendet werden.The active compound combinations can be used as such, in the form of concentrates or generally customary formulations such as powders, granules, solutions, suspensions, emulsions or pastes.
Die genannten Formulierungen können in an sich bekannter Weise hergestellt werden, z.B. durch Vermischen der Wirkstoffe mit mindestens einem Lösungs- bzw. Verdünnungsmittel, Emulgator, Dispergier- und/oder Binde- oder Fixiermittels, Wasser-Repellent, gegebenenfalls Sikkative und UV- Stabilisatoren und gegebenenfalls Farbstoffen und Pigmenten sowie weiteren Verarbeitungshilfsmitteln. Die gute fungizide Wirkung der erfϊndungsgemäßen Wirkstofϊkombinationen geht aus den nachfolgenden Beispielen hervor. Während die einzelnen Wirkstoffe in der fungiziden Wirkung Schwächen aufweisen, zeigen die Kombinationen eine Wirkung, die über eine einfache Wirkungssurnmierung hinausgeht.The formulations mentioned can be prepared in a manner known per se, for example by mixing the active compounds with at least one solvent or diluent, emulsifier, dispersing and / or binding or fixing agent, water repellent, optionally siccatives and UV stabilizers and optionally Dyes and pigments and other processing aids. The good fungicidal action of the active compound combinations according to the invention is evident from the examples below. While the individual active ingredients have weaknesses in the fungicidal action, the combinations show an effect that goes beyond a simple effect of turning.
Ein synergistischer Effekt liegt bei Fungiziden immer dann vor, wenn die fungizide Wirkung der Wirkstofϊkombinationen größer ist als die Summe der Wirkungen der einzeln applizierten Wirkstoffe.A synergistic effect is always present in fungicides when the fungicidal action of the drug combinations is greater than the sum of the effects of the individually applied active ingredients.
Die zu erwartende fungizide Wirkung für eine gegebene Kombination zweier Wirkstoffe kann nach S.R. Colby („Calculating Synergistic and Antagonistic Responses of Herbicide Combinations", Weeds IMZ, 15.20-22) wie folgt berechnet werden:The expected fungicidal effect for a given combination of two drugs can be found in S.R. Colby ("Calculating Synergistic and Antagonistic Responses of Herbicidal Combinations", Weeds IMZ, 15.20-22) are calculated as follows:
WennIf
X den Wirkungsgrad beim Einsatz des Wirkstoffes A in einer Aufwandmenge von m ppm bedeutet,X means the efficiency when using the active ingredient A in an application rate of m ppm,
Y den Wirkungsgrad beim Einsatz des Wirkstoffes B in einer Aufwandmenge von n ppm bedeutet undY means the efficiency when using the active ingredient B in an application rate of n ppm and
E den Wirkungsgrad beim Einsatz der Wirkstoffe A und B in Aufwandmengen von m und n ppm bedeutet,E means the efficiency when using the active compounds A and B in application rates of m and n ppm,
XxY dann ist E = X+ Y-XxY then E = X + Y-
100100
Dabei wird der Wirkungsgrad in % ermittelt. Es bedeutet 0 % ein Wirkungsgrad, der demjenigen der Kontrolle entspricht, während ein Wirkungsgrad von 100 % bedeutet, dass kein Befall beobachtet wird.The efficiency is determined in%. It means 0% an efficiency that corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
Ist die tatsächliche fungizide Wirkung größer als berechnet, so ist die Kombination in ihrer Wirkung überadditiv, d.h. es liegt ein synergistischer Effekt vor. In diesem Fall muss der tatsächlich beobachtete Wirkungsgrad größer sein als der aus der oben angeführten Formel errechnete Wert für den erwarteten Wirkungsgrad (E). - -If the actual fungicidal effect is greater than calculated, the combination is over-additive in its effect, ie there is a synergistic effect. In this case, the actual observed efficiency must be greater than the expected efficiency value (E) calculated from the above formula. - -
Anwendungsbeispieleapplications
Beispiel AExample A
Puccinia-Test (Weizen) / protektivPuccinia test (wheat) / protective
Lösungsmittel: 50 Gewichtsteile N,N-DimethylacetamidSolvent: 50 parts by weight of N, N-dimethylacetamide
Emulgator: 1 Gewichtseile AlkylarylpolyglykoletherEmulsifier: 1 weight of alkylaryl polyglycol ether
Zur Herstellung einer zweckmäßigen Wirkstoffzubereitung vermischt man 1 Gewichtsteil Wirkstoff mit den angegebenen Mengen Lösungsmittel und Emulgator oder eine handelsübliche Formulierung von Wirkstoff und verdünnt das Konzentrat mit Wasser auf die gewünschte KonzentrationTo prepare a suitable preparation of active compound, 1 part by weight of active compound with the stated amounts of solvent and emulsifier or a commercial formulation of active ingredient and the concentrate is diluted with water to the desired concentration
Zur Prüfung auf protektive Wirksamkeit werden junge Pflanzen mit der Wirkstoffzubereitung in der angegebenen Aufwandmenge besprüht. Nach Antrocknen des Spritzbelages werden die Pflanzen mit einer Konidiensuspension von Puccinia recondita besprüht. Die Pflanzen verbleiben 48 Stunden beiTo test for protective activity, young plants are sprayed with the preparation of active compound in the stated application rate. After the spray coating has dried on, the plants are sprayed with a conidia suspension of Puccinia recondita. The plants remain for 48 hours
200C und 100 % relativer Luftfeuchtigkeit in einer Inkubationskabine.20 0 C and 100% relative humidity in an incubation cabin.
Die Pflanzen werden dann in einem Gewächshaus bei einer Temperatur von ca. 200C und einer relativen Luftfeuchtigkeit von 80 % aufgestellt, um die Entwicklung von Rostpusteln zu begünstigen.The plants are then placed in a greenhouse at a temperature of about 20 0 C and a relative humidity of 80% to promote the development of rust pustules.
10 Tage nach der Inokulation erfolgt die Auswertung. Dabei bedeutet 0 % ein Wirkungsgrad, der demjenigen der Kontrolle entspricht, während ein Wirkungsgrad von 100 % bedeutet, daß kein Befall beobachtet wird.10 days after the inoculation the evaluation takes place. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
Tabelle A: Puccinia-Test (Weizen) protektivTable A: Puccinia test (wheat) protective
gef. = gefundene Wirkung gef. = found effect
** ber. = nach der Colby-Formel berechnete Wirkung - -** calc. = calculated according to the Colby formula - -
Beispiel BExample B
Erysiphe-Test (Weizen) / protektivErysiphe test (wheat) / protective
Lösungsmittel: 50 Gew.-TeileN,N-DimethylacetamidSolvent: 50 parts by weight of N, N-dimethylacetamide
Emulgator: 1 Gew.-Teile AlkylarylpolyglykoletherEmulsifier: 1 part by weight of alkylaryl polyglycol ether
Zur Herstellung einer zweckmäßigen Wirkstoffzubereitung vermischt man 1 Gewichtsteil Wirkstoff mit den angegebenen Mengen Lösungsmittel und Emulgator oder eine handelsübliche Formulierung von Wirkstoff und verdünnt das Konzentrat mit Wasser auf die gewünschte KonzentrationTo prepare a suitable preparation of active compound, 1 part by weight of active compound with the stated amounts of solvent and emulsifier or a commercial formulation of active ingredient and the concentrate is diluted with water to the desired concentration
Zur Prüfung auf protektive Wirksamkeit besprüht man junge Pflanzen mit der Wirkstoffzubereitung in der angegebenen Aufwandmenge.To test for protective activity, young plants are sprayed with the preparation of active compound in the stated application rate.
Nach Antrocknen des Spritzbelages werden die Pflanzen mit Sporen von Erysiphe graminis f.sp. tritici bestäubt.After the spray coating has dried, the plants are spotted with spores of Erysiphe graminis f.sp. tritici pollinated.
Die Pflanzen werden in einem Gewächshaus bei einer Temperatur von ca. 200C und einer relativenThe plants are grown in a greenhouse at a temperature of about 20 0 C and a relative
Luftfeuchtigkeit von ca. 80 % aufgestellt, um die Entwicklung von Mehltaupusteln zu begünstigen.Humidity of about 80% set up to favor the development of powdery mildew pustules.
7 Tage nach der Inokulation erfolgt die Auswertung. Dabei bedeutet 0 % ein Wirkungsgrad, der demjenigen der Kontrolle entspricht, während ein Wirkungsgrad von 100 % bedeutet, daß kein Befall beobachtet wird.7 days after the inoculation the evaluation takes place. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
Tabelle B: Erysiphe-Test (Weizen) protektivTable B: Erysiphe test (wheat) protective
gef. = gefundene Wirkung gef. = found effect
** ber. = nach der Colby-Formel berechnete Wirkung ** calc. = calculated according to the Colby formula

Claims

Patentansprüche claims
1. Fungizide Wirkstoffkombinationen enthaltend das Carboxamid (1-1) N-[2-(l,3-Dimethyl- butyl)-3-thienyl]-l-methyl-3-(trifluoπnethyl)-lH-pyrazol-4-carboxamid und mindestens einen Wirkstoff, der aus der folgenden Liste ausgewählt ist:1. Fungicidal active ingredient combinations containing the carboxamide (1-1) N- [2- (l, 3-dimethyl-butyl) -3-thienyl] -1-methyl-3- (trifluoromethyl) -1H-pyrazole-4-carboxamide and at least one active substance selected from the following list:
(2-1) Fluoxastrobin, (2-2) (2^-2<2-{[6-(3-CMor-2-me%lphenoxy)-5-fluor4-pyrirnidinyl]- oxy}phenyl)-2-(methoxyimino)-N-methylethanarnid, (2-3) Trifloxystrobin, (2-4) (2£)-2-(Meth- oxyimino)-N-methyl-2-(2- {[( [(IE)-I -[3-(trifluormetbyl)phenyl]ethyliden} amino)oxy]methyl}- phenyl)ethanamid, (2-5) (2^-2-(Methoxyimino)-N-methyl-2-{2-[(^-({l-[3-(trifluoime%l)- phenyl]etiioxy}irnino)rnethyl]phenyl}ethanarnid, (2-6) Orysastrobin, (2-7) 5-Methoxy-2-me-(2-1) fluoxastrobin, (2-2) (2 ^ -2 <2 - {[6- (3-CMor-2-me% lphenoxy) -5-fluoro-4-pyrirnidinyl] oxy} phenyl) -2- (methoxyimino) -N-methylethanamide, (2-3) trifloxystrobin, (2-4) (2E) -2- (methoxyimino) -N-methyl-2- (2- {[([(IE) - I - [3- (trifluoromethyl) phenyl] ethylidene} amino) oxy] methyl} phenyl) ethanamide, (2-5) (2 ^ -2- (methoxyimino) -N-methyl-2- {2 - [(^ - ({1- [3- (trifluoro-1% -phenyl] -etiioxy} -nino) -ethyl] -phenyl} -ethanarnide, (2-6) orysastrobin, (2-7) 5-methoxy-2-methyl-
%l-4-(2-{[({(l^-l-[3<trifluoπneÜiyl)phenyl]e%liden}arnino)oxy]methyl}phenyl)-2,4-dihy- dro-3H-l,2,4-triazol-3-on, (2-8) Dimoxystrobin, (2-9) Picoxystrobin, (2-10) Pyraclostrobin, (3-1) Azaconazole, (3-2) Etaconazole, (3-3) Propiconazole, (3-4) Difenoconazole, (3-5) Bromu- conazole, (3-6) Cyproconazole, (3-7) Ηexaconazole, (3-8) Penconazole, (3-9) Myclobutanil, (3-10) Tetraconazole, (3-11) Flutriafol, (3-12) Epoxiconazole, (3-13) Flusilazole, (3-14) Sime- conazole, (3-15) Protbioconazole, (3-16) Fenbuconazole, (3-17) Tebuconazole, (3-18) Ipcon- azole, (3-19) Metconazole, (3-20) Triticonazole, (3-21) Bitertanol, (3-22) Triadimenol, (3-23) Triadimefon, (3-24) Fluquinconazole, (3-25) Quinconazole, (4-1) Dichlofluanid, (4-2) Tolylflu- anid, (5-1) Iprovalicarb, (5-2) Benthiavalicarb, (6-1) 2-Chloro-Ν-(l,l,3-trimethyl-indan-4-yl)- nicotinamid, (6-2) Boscalid, (6-3) Furametpyr, (6-4) Ethaboxam, (6-5) Fenhexamid, (6-6) Car- propamid, (6-7) 2-CUor-4-(2-fluor-2-methyl-propionylarnino)-N,N-dimetlτyl-benzamid, (6-8) Picobenzamid, (6-9) Zoxamide, (6-10) S^-Dichlor-N^-cyanopheny^isothiazol-S-carboxamid, (6-11) Carboxin, (6-12) Tiadinil, (6-13) Silthiofam, (7-1) Mancozeb, (7-2) Maneb, (7-3) Meti- ram, (7-4) Propineb, (7-5) Tbiram, (7-6) Zineb, (7-7) Ziram, (8-1) Benalaxyl, (8-2) Furalaxyl, (8-3) Benalaxyl-M, (9-1) Cyprodinil, (9-2) Pyrimethanil, (10-1) 6-Chlor-5-[(3,5-dimethylisoxa- zol-4-yl)sulfonyl]-2,2-difluor-5Η-[l,3]dioxolo[4,5-fJbenzimidazol, (10-2) Benomyl, (10-3) Car- bendazim, (10-4) Chlorfenazole, (10-5) Fύberidazole, (10-6) Thiabendazole, (11-1) Propamo- carb, (11-2) Propamocarb-hydrochloride, (11-3) Propamocarb-Fosetyl, (12-1) Captafol, (12-2) Folpet, (12-3) Iprodione, (12-4) Procymidone, (12-5) Vinclozolin, (13-1) Dodine, (13-2) Guazatine, (13-3) Iminoctadine triacetate, (14-1) Cyazofamid, (14-2) Prochloraz, (14-3)% I-4- (2 - {[({(1-yl-3-trifluorophenyl) -yl] -phenyl] e-halo} -arynino) oxy] -methyl} -phenyl) -2,4-dihydro-3H-1, 2,4-triazol-3-one, (2-8) dimoxystrobin, (2-9) picoxystrobin, (2-10) pyraclostrobin, (3-1) azaconazole, (3-2) etaconazole, (3-3) Propiconazole, (3-4) difenoconazole, (3-5) bromo-conazole, (3-6) cyproconazole, (3-7) exaconazole, (3-8) penconazole, (3-9) myclobutanil, (3-10 ) Tetraconazole, (3-11) flutriafol, (3-12) epoxiconazole, (3-13) flusilazole, (3-14) simeconazole, (3-15) protbioconazole, (3-16) fenbuconazole, (3- 17) tebuconazole, (3-18) ipconazole, (3-19) metconazole, (3-20) triticonazole, (3-21) bitertanol, (3-22) triadimenol, (3-23) triadimefon, (3 -24) Fluquinconazole, (3-25) Quinconazole, (4-1) Dichlofluanid, (4-2) Tolylfluidide, (5-1) Iprovalicarb, (5-2) Benthiavalicarb, (6-1) 2-Chloro -Ν- (l, l, 3-trimethyl-indan-4-yl) nicotinamide, (6-2) boscalid, (6-3) furametpyr, (6-4) ethaboxam, (6-5) fenhexamide, ( 6-6) carboxamide, (6-7) 2-Cuor-4- (2-fluoro-2-methyl-propionyl-amino) -N, N-dim ethyl-benzamide, (6-8) picobenzamide, (6-9) zoxamides, (6-10) S, -dichloro-N, -cyanophenyl, isothiazole-S-carboxamide, (6-11) carboxin, (6-12 ) Tiadinil, (6-13) Silthiofam, (7-1) Mancozeb, (7-2) Maneb, (7-3) Metiram, (7-4) Propineb, (7-5) Tbiram, (7 6) zineb, (7-7) ziram, (8-1) benalaxyl, (8-2) furalaxyl, (8-3) benalaxyl-M, (9-1) cyprodinil, (9-2) pyrimethanil, (10 -1) 6-chloro-5 - [(3,5-dimethylisoxazol-4-yl) sulfonyl] -2,2-difluoro-5Η- [1,3] dioxolo [4,5-f-benzimidazole, (10 2) benomyl, (10-3) carbendazim, (10-4) chlorfenazoles, (10-5) fύberidazoles, (10-6) thiabendazoles, (11-1) propamocarb, (11-2) propamocarb hydrochloride, (11-3) propamocarb-fosetyl, (12-1) captafol, (12-2) folpet, (12-3) iprodione, (12-4) procymidone, (12-5) vinclozolin, (13-1 ) Dodine, (13-2) guazatine, (13-3) iminoctadine triacetate, (14-1) cyazofamide, (14-2) prochloraz, (14-3)
Triazoxide, (14-4) Peforazoate, (15-1) Aldimorph, (15-2) Tridemoφh, (15-3) Dodemorph, (15-4) Fenpropimorph, (16-1) Fenpiclonil, (16-2) Pyrrolnitrine, (17-1) Phosphonic acid, (18-1) 2-(2,3-Dihydro-lH-mden-5-yl)-N-[2-(34-dimethoxyph^ (18-2) N-[2-(3,4-Dimethoxyphenyl)ethyl]-2-(methoxyirnino)-2-(5,6,7,8-tetrahydronaphthalen-2- yl)acetamid, (18-3) 2-(4-(^oφhenyl)-N-[2-(3,4-dime1hoxyphenyl)e%l]-2-(methoxyirnino)- acetamid, (18-4) 2-(4-Bromphenyl)-N-[2-(3,4-dime1hoxyphenyl)ethyl]-2-(methoxyirnino)acet- amid, (18-5) 2-(4-Methylphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(methoxyinτino)acet- amid, (18-6) 2-(4-Ethylphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(methoxyimino)acetaπüd, (19-1) Acibenzolar-S-methyl, (19-2) Edifenphos, (19-3) Famoxadone, (19-4) Oxadixyl, (19-5) Spiroxamine, (19-6) Dithianon, (19-7) Metrafenone, (19-8) Fenamidone, (19-9) 2,3-Dibutyl-6- chlor-thieno[2,3-d]pyrimidin-4(3H)on, (19-10) Probenazole, (19-11) boprothiolane, (19-12)Triazoxide, (14-4) peforazoate, (15-1) aldimorph, (15-2) tridemoφh, (15-3) dodemorph, (15-4) fenpropimorph, (16-1) fenpiclonil, (16-2) pyrrole-nitrine , (17-1) phosphonic acid, (18-1) 2- (2,3-dihydro-1H-mden-5-yl) -N- [2- (34-dimethoxyph- (18-2) N- [ 2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxy-4-amino) -2- (5,6,7,8-tetrahydronaphthalen-2-yl) -acetamide, (18-3) 2- (4 - (o-phenyl) ) -N- [2- (3,4-dime1hoxyphenyl) e] -] - (methoxy-4-amino) -acetamide, (18-4) 2- (4-bromophenyl) -N- [2- (3,4-) dime1hoxyphenyl) ethyl] -2- (methoxyirnino) acetaldehyde amide, (18-5) 2- (4-methylphenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxyquinoo) acetamide, (18-6) 2- (4-ethylphenyl ) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxyimino) acetapyridine, (19-1) acibenzolar-S-methyl, (19-2) edifenphos, (19-3) famoxadone, ( 19-4) oxadixyl, (19-5) spiroxamine, (19-6) dithianone, (19-7) metrafenone, (19-8) fenamidone, (19-9) 2,3-dibutyl-6-chlorothieno [2,3-d] pyrimidin-4 (3H) on, (19-10) Probenazoles, (19-11) boprothiolanes, (19-12)
Kasugamycin, (19-13) Phthalide, (19-14) N-({4-[(Cyclopropylamino)carbonyl]pheriyl}sul- fonyl)-2-methoxybenzanτid, (19-15) 2-(4-Chloφhenyl)-N-{2-[3-methoxy-4-(prop-2-in-l-yloxy)- phenyl]ethyl}-2-(prop-2-in-l-yloxy)acetamid, (19-16) Quinoxyfen, (19-17) Proquinazid, (20-1) Pencycuron, (20-2) Tbiophanate-e%l, (21-1) Fenoxanil, (21-2) Diclocymet, (22-1) 5-Chlor-N- [(7Ä>2,2,2-ttfluor-l-methyle%l]-6-(2,4,6-1rifluoφhenyl)[l,2,4]1τiazolo[l,5-a]pyrirni amin, (22-2) 5-Chlor-N-[(7i?;-l ,2-dimethylpropyl]-6-(2,4,6-trifluorphenyl)[l,2,4]triazolo[l,5-a]- pyrimidin-7-amin, (22-3) 5-Chlόr-6-(2-chlor-6-fluorphenyl)-7-(4-methylpiperidin-l-yl)[l,2,4]tri- azolo[l,5-a]pyritnidin, (22-4) 5-Chlor-6-(2,4,6-trifluoφhenyl)-7-(4-methylpiperidin-l-yl)- [l,2,4]triazolo[l,5-a]pyrimidin, (22-5) 5-Chlor-6-(2,4,6-trifluoφhenyl)-N-[(i5)-l,2,2-triniethyl- propyl][l,2,4]triazolo[l,5-a]pyrimidin-7-amin, (23-1) 2-Butoxy-6-iod-3-propyl-benzopyran-4- on, (23-2) 2-Ethoxy-6-iod-3-propyl-benzopyran-4-on, (23-3) 6-Iod-2-propoxy-3-propyl-benzo- pyran-4-on, (23-4) 2-But-2-inyloxy-6-iod-3-propyl-benzopyran-4-on, (23-5) 6-Iod-2-(l-methyl- butoxy)-3-propyl-benzopyran-4-on, (23-6) 2-But-3-enyloxy-6-iod-benzopyran-4-on, (23-7) 3- Butyl-6-iod-2-isopropoxy-benzopyran-4-on.Kasugamycin, (19-13) phthalides, (19-14) N - ({4 - [(cyclopropylamino) carbonyl] pheriyl} sulfonyl) -2-methoxybenzanovid, (19-15) 2- (4-chlorophenyl) - N- {2- [3-methoxy-4- (prop-2-yn-1-yloxy) -phenyl] ethyl} -2- (prop-2-yn-1-yloxy) acetamide, (19-16) quinoxyfen , (19-17) proquinazide, (20-1) pencycuron, (20-2) biophanate-e% l, (21-1) fenoxanil, (21-2) diclocymet, (22-1) 5-chloro-N - [(7A> 2,2,2-t-fluoro-1-methyl-1-yl] -6- (2,4,6-trifluoro-phenyl) [l, 2,4] 1-tiazolo [l, 5-a] pyrimidinium, ( 22-2) 5-Chloro-N - [(7-α, -l, 2-dimethyl-propyl] -6- (2,4,6-trifluorophenyl) [l, 2,4] triazolo [l, 5-a] - pyrimidin-7-amine, (22-3) 5-chloro-6- (2-chloro-6-fluorophenyl) -7- (4-methylpiperidin-1-yl) [l, 2,4] triazolo [l , 5-a] pyritnidine, (22-4) 5-chloro-6- (2,4,6-trifluorophenyl) -7- (4-methylpiperidin-1-yl) - [l, 2,4] triazolo [l , 5-a] pyrimidine, (22-5) 5-chloro-6- (2,4,6-trifluorophenyl) -N - [(i5) -l, 2,2-triethyl-propyl] [l, 2, 4] triazolo [l, 5-a] pyrimidin-7-amine, (23-1) 2-butoxy-6-iodo-3-propyl-benzopyran-4-one, (23-2) 2-ethoxy-6- iodo-3-propyl-benzopyran-4-one, (23-3) 6-iodo-2-p ropoxy-3-propyl-benzopyran-4-one, (23-4) 2-but-2-ynyloxy-6-iodo-3-propyl-benzopyran-4-one, (23-5) 6-iodo 2- (1-methylbutoxy) -3-propylbenzopyran-4-one, (23-6) 2-but-3-enyloxy-6-iodobenzopyran-4-one, (23-7) 3- butyl-6-iodo-2-isopropoxy-benzopyran-4-one.
2. Fungizide Wirkstoffkombinationen enthaltend ein Carboxamid der allgemeinen Formel (I) (Gruppe 1)2. Fungicidal active substance combinations containing a carboxamide of the general formula (I) (group 1)
(I), in welcher(I), in which
R für Wasserstoff oder Methyl steht, G für Wasserstoff, Fluor oder Methyl steht,R is hydrogen or methyl, G is hydrogen, fluorine or methyl,
R1 für Wasserstoff, Halogen, Ci-C3-Alkyl oder CrC3-Halogenalkyl mit 1 bis 7 Fluor-,R 1 represents hydrogen, halogen, Ci-C 3 alkyl or C r C 3 -haloalkyl having 1 to 7 fluorine,
Chlor- und/oder Bromatomen steht, A für einen der folgenden Reste Al oder A2 steht:Chlorine and / or bromine atoms, A is one of the following radicals Al or A2:
X für CH oder N steht, R2 für Methyl, Difluorme%l oder Trifluormethyl steht, X is CH or N, R 2 is methyl, difluoromethylene or trifluoromethyl,
R3 für Wasserstoff oder Fluor steht,R 3 is hydrogen or fluorine,
R4 für Difluormethyl oder Trifluormethyl steht,R 4 is difluoromethyl or trifluoromethyl,
und mindestens einen Wirkstoff, der aus den folgenden Gruppen (2) bis (23) ausgewählt ist:and at least one active ingredient selected from the following groups (2) to (23):
Gruppe (2) StrobilurineGroup (2) strobilurins
(2-1) Fluoxastrobin, (2-2) (2J&)-2-(2-{[6-(3-Chlor-2-methylphenoxy)-5-fluor-4-pyrimidinyl]- oxy}phenyl)-2-(methoxyimino)-N-memylethanamid, (2-3) Trifloxystrobin, (2-4) (2£)-2-(Meth- oxyimino)-N-methyl-2-(2-{[({(1^4-[3-(1xifluomiemyl)phenyl]e%liden}amino)oxy3me%l}- phenyl)ethanamid, (2-5) (2^-2-(Memoxyimino)-N-methyl-2-{2-[(-7)-({l-[3-(trifluorme%l)- phenyl]emoxy}imino)methyl]phenyl}ethanamid, (2-6) Orysastrobin, (2-7) 5-Methoxy-2-me- thyM-(2-{[({(l^-l-[3-(trifluoraiethyl)phenyl]e%liden}arnino)oxy]methyl}phenyl)-2,4-dihy- dro-3H-l,2,4-triazol-3-on, (2-8) Dimoxystrobin, (2-9) Picoxystrobin, (2-10) Pyraclostrobin, Gruppe (3) Triazole(2-1) fluoxastrobin, (2-2) ( 2J &) - 2- (2 - {[6- (3-chloro-2-methylphenoxy) -5-fluoro-4-pyrimidinyl] oxy} phenyl) -2- (methoxyimino) -N-memylethaneamide, (2-3) trifloxystrobin, (2-4) (2E) -2- (methoxyimino) -N-methyl-2- (2 - {[({( 1 ^ 4- [3- (1-fluoromethyl) -phenyl] e-1-halo} amino) oxy-3-yl-1-1-phenyl) -ethaneamide, (2-5) (2 ^ -2- (memoxyimino) -N-methyl-2- {2 - [(- 7) - ({1- [3- (trifluoromethyl) -1-phenyl] -emoxy} -imino) methyl] -phenyl} -ethaneamide, (2-6) orysastrobin, (2-7) 5-methoxy-2- methyl- (2 - {[({(1-yl-3- (trifluoro-ethyl) -phenyl] e-halo} -arynino) oxy] -methyl} -phenyl) -2,4-dihydro-3H-1, 2,4-triazol-3-one, (2-8) dimoxystrobin, (2-9) picoxystrobin, (2-10) pyraclostrobin, group (3) triazoles
(3-1) Azaconazole, (3-2) Etaconazole, (3-3) Propiconazole, (3-4) Difenoconazole, (3-5) Bromu- conazole, (3-6) Cyproconazole, (3-7) Ηexaconazole, (3-8) Penconazole, (3-9) Myclobutanil, (3- 10) Tetraconazole, (3-11) Flutriafol, (3-12) Epoxiconazole, (3-13) Flusilazole, (3-14) Simeconazole, (3-15) Prothioconazole, (3-16) Fenbuconazole, (3-17) Tebuconazole, (3-18) Ipconazole, (3-19) Metconazole, (3-20) Triticonazole, (3-21) Bitertanol, (3-22) Triadimenol, (3-(3-1) azaconazole, (3-2) etaconazole, (3-3) propiconazole, (3-4) difenoconazole, (3-5) bromo-conazole, (3-6) cyproconazole, (3-7) exaconazole , (3-8) penconazoles, (3-9) myclobutanil, (3-10) tetraconazoles, (3-11) flutriafol, (3-12) epoxiconazoles, (3-13) flusilazoles, (3-14) simeconazoles, (3-15) prothioconazole, (3-16) fenbuconazole, (3-17) tebuconazole, (3-18) ipconazole, (3-19) metconazole, (3-20) triticonazole, (3-21) bitertanol, ( 3-22) Triadimenol, (3
23) Triadimefon, (3-24) Fluquinconazole, (3-25) Quinconazole, Gruppe (4) Sulfenamide (4-1) Dichlofluanid, (4-2) Tolylfluanid, Gruppe (5) Valinamide (5-1) Iprovalicarb, (5-2) Benthiavalicarb,23) triadimefon, (3-24) fluquinconazole, (3-25) quinconazole, group (4) sulfenamide (4-1) dichlofluanid, (4-2) tolylfluanid, group (5) valinamide (5-1) iprovalicarb, ( 5-2) benthiavalicarb,
Gruppe (6) CarboxamideGroup (6) carboxamides
(6-1) 2-GMoro-N-(l,l,3-trime%l-indan-4-yl)-nicotinamid, (6-2) Boscalid, (6-3) Furametpyr, (6-4) Ethaboxam, (6-5) Fenhexamid, (6-6) Carpropamid, (6-7) 2-Chlor-4-(2-fluor-2-methyl- propionylamino)-Ν,Ν-dimethyl-benzamid, (6-8) Picobenzamid, (6-9) Zoxamide, (6-10) 3,4- Dichlor-N-(2-cyanophenyl)isothiazol-5-carboxamid, (6-11) Carboxin, (6-12) Tiadinil, (6-13)(6-1) 2-GMoro-N- (1,1,3-trimethylene-1-indan-4-yl) -nicotinamide, (6-2) boscalid, (6-3) furametpyr, (6-4) Ethaboxam, (6-5) fenhexamide, (6-6) carpropamide, (6-7) 2-chloro-4- (2-fluoro-2-methylpropionylamino) -Ν, Ν-dimethylbenzamide, (6- 8) Picobenzamide, (6-9) Zoxamides, (6-10) 3,4-Dichloro-N- (2-cyanophenyl) isothiazole-5-carboxamide, (6-11) Carboxine, (6-12) Tiadinil, ( 6-13)
Silthiofam,silthiofam,
Gruppe (7) DithiocarbamateGroup (7) dithiocarbamates
(7-1) Mancozeb, (7-2) Maneb, (7-3) Metiram, (7-4) Propineb, (7-5) Thiram, (7-6) Zineb, (7-7) Ziram, Gruppe (8) Acylalanine(7-1) mancozeb, (7-2) maneb, (7-3) metiram, (7-4) propineb, (7-5) thiram, (7-6) zineb, (7-7) ziram, group (8) acylalanines
(8-1) Benalaxyl, (8-2) Furalaxyl, (8-3) Benalaxyl-M, Gruppe (9): Anilino-pyrimidine(8-1) benalaxyl, (8-2) furalaxyl, (8-3) benalaxyl-M, Group (9): anilino-pyrimidines
(9-1) Cyprodinil, (9-2) Pyrimethanil,(9-1) cyprodinil, (9-2) pyrimethanil,
Gruppe (IQ"): BenzimidazoleGroup (IQ " ): benzimidazoles
(10-1) 6-Chlor-5-[(3,5-dimethylisoxazol-4-yl)sulfonyl]-2,2-difluor-5H-[l,3]dioxolo[4,5-f|benz- imidazol, (10-2) Benomyl, (10-3) Carbendazim, (10-4) Chlorfenazole, (10-5) Fuberidazole,(10-1) 6-Chloro-5 - [(3,5-dimethylisoxazol-4-yl) sulfonyl] -2,2-difluoro-5H- [1,3] dioxolo [4,5-f-benzimidazole , (10-2) benomyl, (10-3) carbendazim, (10-4) chlorfenazoles, (10-5) fuberidazoles,
(10-6) Thiabendazole,(10-6) Thiabendazole,
Gruppe dl): CarbamateGroup dl): carbamates
(11-1) Propamocarb, (11-2) Propamocarb-hydrochloride, (11-3) Propamocarb-Fosetyl,(11-1) propamocarb, (11-2) propamocarb-hydrochloride, (11-3) propamocarb-fosetyl,
Gruppe (12): Dicarboximide (12-1) Captafol, (12-2) Folpet, (12-3) Iprodione, (12-4) Procymidone, (12-5) Vinclozolin,Group (12): dicarboximide (12-1) captafol, (12-2) folpet, (12-3) iprodione, (12-4) procymidone, (12-5) vinclozolin,
Gruppe (13): GuanidineGroup (13): guanidines
(13-1) Dodine, (13-2) Guazatine, (13-3) Iminoctadine triacetate,(13-1) dodine, (13-2) guazatine, (13-3) iminoctadine triacetate,
Gruppe (14): ImidazoleGroup (14): imidazoles
(14-1) Cyazofamid, (14-2) Prochloraz, (14-3) Triazoxide, (14-4) Pefurazoate, Gruppe (15): Morpholine(14-1) cyazofamide, (14-2) prochloraz, (14-3) triazoxide, (14-4) pefurazoate, group (15): morpholine
(15-1) Aldimorph, (15-2) Tridemorph, (15-3) Dodemoφh, (15-4) Fenpropimorph,(15-1) aldimorph, (15-2) tridemorph, (15-3) dodemoφh, (15-4) fenpropimorph,
Gruppe (16): PyrroleGroup (16): Pyrroles
(16-1) Fenpiclonil, (16-2) Pyrrolnitrine,(16-1) fenpiclonil, (16-2) pyrrole-nitrine,
Gruppe ("17): Phosphonate (17-1) Phosphonic acid,Group ( " 17): phosphonates (17-1) phosphonic acid,
Gruppe (18): PhenylethanamideGroup (18): phenylethanamides
(18-1) 2-(2,3-Dihydro-lH-inden-5-yl)-N-[2-(3,4-dimethoxyphenyl)e%l]-2-(rnethoxyimino)- acetamid, (18-2) N-[2-(3,4-Dimethoxyphenyl)e%l]-2-(methoxyirnino)-2-(5,6,7,8-tetrahydro- naphthalen-2-yl)acetamid, (18-3) 2-(4-Chlorphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2- (methoxyimino)acetamid, (18-4) 2-(4-Bromphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(18-1) 2- (2,3-dihydro-1H-inden-5-yl) -N- [2- (3,4-dimethoxyphenyl) e] -1- (2-methoxyimino) acetamide, (18 -2) N- [2- (3,4-dimethoxyphenyl) e] -1- (2-methoxyimino) -2- (5,6,7,8-tetrahydronaphthalen-2-yl) acetamide, (18- 3) 2- (4-chlorophenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2- (methoxyimino) acetamide, (18-4) 2- (4-bromophenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2-
(methoxyimino)acetamid, (18-5) 2-(4-Methylphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(methoxyimino) acetamide, (18-5) 2- (4-methylphenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2-
(metb.oxyimino)acetamid, (18-6) 2-(4-Ethylphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(metb.oxyimino) acetamide, (18-6) 2- (4-ethylphenyl) -N- [2- (3,4-dimethoxyphenyl) ethyl] -2-
(methoxyimino)acetamid,(Methoxyimino) acetamide,
Gruppe (19): Fungizide (19-1) Acibenzolar-S-methyl, (19-2) Edifenphos, (19-3) Famoxadone, (19-4) Oxadixyl, (19-5)Group (19): fungicides (19-1) acibenzolar-S-methyl, (19-2) edifenphos, (19-3) famoxadone, (19-4) oxadixyl, (19-5)
Spiroxamine, (19-6) Dithianon, (19-7) Metrafenone, (19-8) Fenamidone, (19-9) 2,3-Dibutyl-6- chlor-tbieno[2,3-d]pyrimidin-4(3H)on, (19-10) Probenazole, (19-11) Isoprotbiolane, (19-12)Spiroxamine, (19-6) dithianone, (19-7) metrafenone, (19-8) fenamidone, (19-9) 2,3-dibutyl-6-chloro-tbieno [2,3-d] pyrimidine-4 ( 3H) on, (19-10) sample azoles, (19-11) isoprotbiolanes, (19-12)
Kasugamycin, (19-13) Phthalide, (19-14) N-({4-[(Cyclopropylamino)carbonyl]phenyl}sulfo- nyl)-2-methoxybenzamid, (19-15) 2-(4-Chlorphenyl)-N-{2-[3-methoxy-4-(prop-2-in-l-yloxy)- phenyl]ethyl}-2-(prop-2-in-l-yloxy)acetamid, (19-16) Quinoxyfen, (19-17) Proquinazid,Kasugamycin, (19-13) phthalides, (19-14) N - ({4 - [(cyclopropylamino) carbonyl] phenyl} sulfonyl) -2-methoxybenzamide, (19-15) 2- (4-chlorophenyl) - N- {2- [3-methoxy-4- (prop-2-yn-1-yloxy) -phenyl] ethyl} -2- (prop-2-yn-1-yloxy) acetamide, (19-16) quinoxyfen , (19-17) Proquinazide,
Gruppe (20): (Thio^Hamstoff-Derivate (20-1) Pencycuron, (20-2) Thiophanate-ethyl, Gruppe (21V. Amide (21-1) Fenoxanil, (21-2) Diclocymet Gruppe (22 V. Triazolopyrimidine (22-1) 5-Cωor-N-[(7S>2,2;2-trifluor-l-me%lethyl]-6-(2,4,6-trifluoφhenyl)[l,2,4]triazolo-Group (20): (thio) urea derivatives (20-1) pencycuron, (20-2) thiophanate-ethyl, group (21V, amide (21-1) fenoxanil, (21-2) diclocymet group (22V. Triazolopyrimidines (22-1) 5-Cω or -N - [(7S> 2,2, 2-trifluoro-l-me% lethyl] -6- (2,4,6-trifluoφhenyl) [l, 2,4] triazolo-
[l,5-a]pyrimidin-7-amin, (22-2) 5-Chlor-N-[fH?)-l,2-dimeihylpropyl]-6-(2,4,6-trifluoφhenyl)- [l,2,4]triazolo[l,5-a]pyrimidin-7-amin, (22-3) 5-Chlor-6-(2-chlor-6-iluoφhenyl)-7-(4-methylpi- peridin-l-yl)[l,2,4]triazolo[l,5-a]pyrimidin, (22-4) 5-Chlor-6-(2,4,6-trifluorphenyl)-7-(4-me- mylpiperidin-l-yl)[l,2,4]triazolo[l,5-a]pyrirnidin, (22-5) 5-CrJor-6-(2,4,6-trifluoφhenyl)-N- [(i5)-l,2,2-trimethylpropyl][l,2,4]triazolo[l,5-a]pyrinτddin-7-amin,[l, 5-a] pyrimidin-7-amine, (22-2) 5-chloro-N- [fH?] - l, 2-dimethylhexylpropyl] -6- (2,4,6-trifluorophenyl) - [l , 2,4] triazolo [l, 5-a] pyrimidin-7-amine, (22-3) 5-chloro-6- (2-chloro-6-iluoφhenyl) -7- (4-methylpiperidine-1 -yl) [l, 2,4] triazolo [l, 5-a] pyrimidine, (22-4) 5-chloro-6- (2,4,6-trifluorophenyl) -7- (4-methylpiperidine) l-yl) [l, 2,4] triazolo [l, 5-a] pyrimidine, (22-5) 5-CrJor-6- (2,4,6-trifluorophenyl) -N- [(i5) -l , 2,2-trimethylpropyl] [l, 2,4] triazolo [l, 5-a] pyrinτddin-7-amine,
Gruppe ("23V. IodochromoneGroup ( " 23V Iodochromone
(23-1) 2-Butoxy-6-iod-3-propyl-benzopyran-4-on, (23-2) 2-Ethoxy-6-iod-3-propyl-benzoρyran- 4-on, (23-3) 6-Iod-2-propoxy-3-propyl-benzopyran-4-on, (23-4) 2-But-2-inyloxy-6-iod-3-propyl- benzopyran-4-on, (23-5) 6-Iod-2-(l-methyl-butoxy)-3-propyl-benzopyran-4-on, (23-6) 2-But-3- enyloxy-6-iod-benzopyran-4-on, (23-7) 3-Butyl-6-iod-2-isopropoxy-benzopyran-4-on.(23-1) 2-Butoxy-6-iodo-3-propyl-benzopyran-4-one, (23-2) 2-ethoxy-6-iodo-3-propyl-benzo-pyran-4-one, (23-3 ) 6-iodo-2-propoxy-3-propylbenzopyran-4-one, (23-4) 2-but-2-ynyloxy-6-iodo-3-propylbenzopyran-4-one, (23-5 ) 6-iodo-2- (1-methyl-butoxy) -3-propyl-benzopyran-4-one, (23-6) 2-but-3-enyloxy-6-iodo-benzopyran-4-one, (23 -7) 3-Butyl-6-iodo-2-isopropoxy-benzopyran-4-one.
3. Wirkstoffkombinationen gemäß Anspruch 2 enthaltend ein Carboxamid der allgemeinen Formel (I) gemäß Anspruch 2 (Gruppe 1), in welcher R für Wasserstoff oder Methyl steht, G für Wasserstoff oder Methyl steht,3. active substance combinations according to claim 2 comprising a carboxamide of the general formula (I) according to claim 2 (group 1), in which R is hydrogen or methyl, G is hydrogen or methyl,
R1 für Wasserstoff, Fluor, Chlor, Methyl, Ethyl, n-, iso-Propyl, Monofluormethyl, Difluormethyl, Trifluormethyl, Monochlormethyl, Dichlormethyl oder Trichlorme- thyl steht, A für einen der folgenden Reste Al oder A2 steht:R 1 is hydrogen, fluorine, chlorine, methyl, ethyl, n-, iso-propyl, monofluoromethyl, difluoromethyl, trifluoromethyl, monochloromethyl, dichloromethyl or trichloromethyl, A is one of the following radicals Al or A2:
X für CH oder N steht,X is CH or N,
R2 für Methyl, Difluormethyl oder Trifluormethyl steht, R3 für Wasserstoff oder Fluor steht, R4 für Difluormethyl oder Trifluormethyl steht.R 2 is methyl, difluoromethyl or trifluoromethyl, R 3 is hydrogen or fluorine, R 4 is difluoromethyl or trifluoromethyl.
4. Wirkstoffkombinationen gemäß Anspruch 2 enthaltend das Carboxamid (1-9) N-[2-(l,3- Dimethylbutyl)-3-thienyl]-5-fluor-l,3-dimethyl-lH-pyrazol-4-carboxamid (Gruppe 1) und mindestens einen Wirkstoff, der aus den folgenden Gruppen (2) bis (23) gemäß Anspruch 2 ausgewählt ist.4. active substance combinations according to claim 2 containing the carboxamide (1-9) N- [2- (l, 3-dimethylbutyl) -3-thienyl] -5-fluoro-l, 3-dimethyl-lH-pyrazole-4-carboxamide ( Group 1) and at least one active ingredient selected from the following groups (2) to (23) according to claim 2.
5. Wirkstoffkombinationen gemäß Anspruch 2 enthaltend das Carboxamid (1-13) N-[2-(l,3- Dimethylbutyl)-3-thienyl]-l-methyl-4-(1rifluoπnethyl)-lH-pyrrol-3-carboxamid (Gruppe 1) und mindestens einen Wirkstoff, der aus den folgenden Gruppen (2) bis (23) gemäß Anspruch 2 ausgewählt ist.5. active substance combinations according to claim 2 comprising the carboxamide (1-13) N- [2- (l, 3-dimethylbutyl) -3-thienyl] -1-methyl-4- (1rifluoπnethyl) -1H-pyrrole-3-carboxamide ( Group 1) and at least one active ingredient selected from the following groups (2) to (23) according to claim 2.
6. Wirkstoffkombinationen gemäß Anspruch 2 enthaltend das Carboxamid (1-25) N-[2-(l,3- Dime1hylbu1yl)-3-iMenyl3-2-methyM-(trifluormemyl)-l,3-thiazol-5-carboxarnid (Gruppe 1) und mindestens einen Wirkstoff, der aus den folgenden Gruppen (2) bis (23) gemäß Anspruch 2 ausgewählt ist.6. active substance combinations according to claim 2 containing the carboxamide (1-25) N- [2- (l, 3-Dime1hylbu1yl) -3-iMenyl3-2-methyl- (trifluoromethyl) -1,3-thiazole-5-carboxamide (group 1) and at least one drug selected from the following groups (2) to (23) according to claim 2.
7. Verwendung von Wirkstoffkombinationen gemäß Anspruch 1 oder 2 zum Bekämpfung von unerwünschten phytopathogenen Pilzen.7. Use of active compound combinations according to claim 1 or 2 for controlling unwanted phytopathogenic fungi.
8. Verwendung von Wirkstoffkombinationen gemäß Anspruch 1 oder 2 zur Behandlung von Saatgut.8. Use of active compound combinations according to claim 1 or 2 for the treatment of seed.
9. Verwendung von Wirkstoffkombinationen gemäß Anspruch 1 oder 2 zur Behandlung von transgenen Pflanzen.9. Use of active compound combinations according to claim 1 or 2 for the treatment of transgenic plants.
10. Verwendung von Wirkstoffkombinationen gemäß Anspruch 1 oder 2 zur Behandlung von Saatgut transgener Pflanzen.10. Use of active compound combinations according to claim 1 or 2 for the treatment of seed transgenic plants.
11. Saatgut, welches mit einer Wirkstoffkombination gemäß Anspruch 1 oder 2 behandelt wurde.11. Seed which has been treated with an active ingredient combination according to claim 1 or 2.
12. Verfahren zum Bekämpfen von unerwünschten phytopathogenen Pilzen, dadurch gekennzeichnet, dass man Wirkstoffkombinationen gemäß Anspruch 1 oder 2 auf die uner- wünschten phytopathogenen Pilze und/oder deren Lebensraum und/oder Saatgut ausbringt.12. A method for controlling unwanted phytopathogenic fungi, characterized in that one applies active compound combinations according to claim 1 or 2 to the unwanted phytopathogenic fungi and / or their habitat and / or seed.
13. Verfahren zum Herstellen von fungiziden Mitteln, dadurch gekennzeichnet, dass man Wirkstoffkombinationen gemäß Anspruch 1 oder 2 mit Streckmitteln und/oder oberflächenaktiven Stoffen vermischt. 13. A process for the production of fungicidal agents, characterized in that mixed active compound combinations according to claim 1 or 2 with extenders and / or surface-active substances.
EP06723755A 2005-04-06 2006-03-27 Synergistic fungicidal active substance combinations Withdrawn EP1871167A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005015677A DE102005015677A1 (en) 2005-04-06 2005-04-06 Synergistic fungicidal drug combinations
PCT/EP2006/002778 WO2006105888A2 (en) 2005-04-06 2006-03-27 Synergistic fungicidal active substance combinations

Publications (1)

Publication Number Publication Date
EP1871167A2 true EP1871167A2 (en) 2008-01-02

Family

ID=36691886

Family Applications (1)

Application Number Title Priority Date Filing Date
EP06723755A Withdrawn EP1871167A2 (en) 2005-04-06 2006-03-27 Synergistic fungicidal active substance combinations

Country Status (12)

Country Link
US (7) US8575064B2 (en)
EP (1) EP1871167A2 (en)
JP (1) JP5101491B2 (en)
KR (1) KR101333550B1 (en)
CN (2) CN102907432A (en)
BR (1) BRPI0607018A2 (en)
CA (3) CA2603223A1 (en)
DE (1) DE102005015677A1 (en)
EA (1) EA014663B1 (en)
MX (1) MX2007012289A (en)
UA (1) UA91854C2 (en)
WO (1) WO2006105888A2 (en)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR036872A1 (en) 2001-08-13 2004-10-13 Du Pont ANTRANILAMIDE COMPOSITE, COMPOSITION THAT INCLUDES IT AND METHOD FOR CONTROLLING AN INVERTEBRATE PEST
DE10228103A1 (en) * 2002-06-24 2004-01-15 Bayer Cropscience Ag Fungicidal active ingredient combinations
US7247647B2 (en) 2003-01-28 2007-07-24 E. I. Du Pont De Nemours And Company Cyano anthranilamide insecticides
DE102004049761A1 (en) * 2004-10-12 2006-04-13 Bayer Cropscience Ag Fungicidal drug combinations
WO2007010036A2 (en) * 2005-07-21 2007-01-25 Basf Aktiengesellschaft Fungicidally active agent
WO2007039214A1 (en) * 2005-09-29 2007-04-12 Syngenta Participations Ag Fungicidal compositions
WO2008006541A2 (en) * 2006-07-12 2008-01-17 Syngenta Participations Ag Method of controlling or preventing pathogenic damage in a plant propagation material
CL2007003329A1 (en) * 2006-11-21 2008-03-24 Mitsui Chemicals Inc COMPOSITION FOR THE CONTROL OF DANE PRODUCED BY INSECTS AND DISEASES IN PLANTS THAT INCLUDES A PENTIOPIRAD COMPOUND AND AT LEAST A FUNGICIDE COMPOSITE DIFFERENT FROM PENTIOPIRAD; METHOD OF PLANT DISEASE CONTROL THAT INCLUDES TO APPLY
WO2008119439A2 (en) * 2007-03-29 2008-10-09 Syngenta Participations Ag Fungicidal compositions comprising a carboxamide derivative, cyprodinil and an unsaturated fatty acid
JP2011511033A (en) * 2008-02-05 2011-04-07 ビーエーエスエフ ソシエタス・ヨーロピア Plant health composition
JP2011511032A (en) * 2008-02-05 2011-04-07 ビーエーエスエフ ソシエタス・ヨーロピア Plant health composition
CN101617668B (en) * 2009-07-07 2012-11-07 陕西汤普森生物科技有限公司 Sterilization composition containing bromothalonil and difenoconazole
CN101653140B (en) * 2009-07-31 2012-12-12 深圳诺普信农化股份有限公司 Compound bactericidal composition containing boscalid
CN101700032B (en) * 2009-11-30 2013-06-26 青岛星牌作物科学有限公司 Bactericidal composition containing thiabendazole and application thereof
EA025427B1 (en) 2009-12-08 2016-12-30 Басф Се Pesticidal mixtures
CN101708003B (en) * 2009-12-23 2013-02-27 深圳诺普信农化股份有限公司 Sterilizing composition containing active ester
CN103190410B (en) * 2010-11-30 2014-11-12 陕西美邦农药有限公司 Synergistic fungicidal composition containing cyprodinil
CN103828825B (en) * 2011-03-19 2015-02-18 陕西汤普森生物科技有限公司 Pesticide composition containing pyraclostrobin and triazoles
JP5940369B2 (en) * 2011-05-27 2016-06-29 石原産業株式会社 How to control plant diseases
CN103155924A (en) * 2011-12-18 2013-06-19 深圳诺普信农化股份有限公司 Sterilization composition containing penthiopyrad
CN103250717A (en) * 2012-02-17 2013-08-21 陕西美邦农药有限公司 Bactericidal composition containing procymidone
PE20190346A1 (en) * 2012-02-27 2019-03-07 Bayer Ip Gmbh ACTIVE COMPOUND COMBINATIONS
CN103314982B (en) * 2012-03-20 2016-06-08 陕西韦尔奇作物保护有限公司 A kind of pesticide composition containing fenhexamid
CN103651389A (en) * 2012-09-07 2014-03-26 陕西美邦农药有限公司 High-efficiency bactericidal composition containing penthiopyrad and triazole
CN103651539B (en) * 2012-09-11 2015-09-09 陕西美邦农药有限公司 A kind of composition pesticide containing pyrrole metsulfovax
CN103651485A (en) * 2012-09-11 2014-03-26 陕西美邦农药有限公司 Efficient bactericidal composition containing penthiopyrad
CN103651451A (en) * 2012-09-19 2014-03-26 陕西美邦农药有限公司 Pesticide composition containing penthiopyrad
CN102870795A (en) * 2012-10-25 2013-01-16 联保作物科技有限公司 Sterilization composition and preparation thereof
CN103891743B (en) * 2012-12-31 2015-06-17 江苏丰登作物保护股份有限公司 Bactericidal composition containing isopyrazam and pyraclostrobin and application thereof
CN103798240B (en) * 2013-03-20 2016-03-02 海南正业中农高科股份有限公司 Composition containing pyrrole metsulfovax and methoxy acrylic sterilization component
CN103988840A (en) * 2013-03-20 2014-08-20 海南正业中农高科股份有限公司 Fungicidal composition containing penthiopyrad and prochloraz
CN103271044B (en) * 2013-06-24 2015-02-11 杭州宇龙化工有限公司 Sterilization composite containing tiadinil and thifluzamide
CN103548840B (en) * 2013-10-29 2014-09-10 江苏七洲绿色化工股份有限公司 Sterilization compound containing benzothiostrobin and difenoconazole and application thereof
CN103975936B (en) * 2014-05-15 2016-07-06 南京南农农药科技发展有限公司 A kind of synergy fungicide composite and its preparation method and application
CN104365609B (en) * 2014-11-21 2015-10-28 北京燕化永乐生物科技股份有限公司 A kind of composite bactericide
CN105248424A (en) * 2015-01-12 2016-01-20 四川利尔作物科学有限公司 Sterilization composition and application thereof
CN105475343A (en) * 2015-12-28 2016-04-13 南京华洲药业有限公司 Bactericidal composition containing silthiopham and penthiopyrad and application thereof
CN105638725A (en) * 2016-01-25 2016-06-08 北京市农林科学院 Pesticide mixture used for preventing and treating plant virus diseases and transmission media
CN105794797A (en) * 2016-05-19 2016-07-27 东莞市瑞德丰生物科技有限公司 Sterilization composition containing flumorph, prothioconazole and penthiopyrad
CN105875630A (en) * 2016-05-26 2016-08-24 南京华洲药业有限公司 Sterilization composition containing hydrofluoroether myco-amide and simeconazole and application of sterilization composition
CN107006500A (en) * 2017-04-28 2017-08-04 广东广康生化科技股份有限公司 Composition pesticide comprising folpet and pyrrole metsulfovax
CN107980786A (en) * 2018-01-18 2018-05-04 兴农药业（中国）有限公司 A kind of composition pesticide containing pyrrole metsulfovax and its application
CN109042677A (en) * 2018-08-24 2018-12-21 广东顾地丰生物科技有限公司 A kind of bactericidal composition, fungicide and its application of the metsulfovax containing pyrrole
AU2019418147A1 (en) * 2018-12-31 2021-08-12 Adama Makhteshim Ltd. Fungicidal mixture
CN109892332A (en) * 2019-03-22 2019-06-18 天津市农药研究所 A kind of pyrrole metsulfovax-cyazofamid suspending agent and preparation method thereof

Family Cites Families (135)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1972961A (en) 1931-05-26 1934-09-11 Du Pont Disinfectant
US2588428A (en) 1945-04-02 1952-03-11 Goodrich Co B F Complex amine products with dialkyl zinc dithiocarbamates as pesticides
US2504404A (en) 1946-06-12 1950-04-18 Du Pont Manganous ethylene bis-dithiocarbamate and fungicidal compositions containing same
AT214705B (en) 1948-05-18 Exxon Research Engineering Co Methods of combating pests
DE1076434B (en) 1957-08-17 1960-02-25 Badische Anilin- S. Soda-Fabrik Aktiengesellschaft, Ludwigshafen/Rhein Fungicides
US3010968A (en) 1959-11-25 1961-11-28 Du Pont Process for manufacture of certain alkyl esters of benzimidazole carbamic acids
DE1151404B (en) 1960-10-13 1963-07-11 Karl Maerkl Fish sorter for sorting out fish according to size or thickness
NL277492A (en) 1960-11-03
NL272405A (en) 1960-12-28
BE614214A (en) 1961-02-22
BE617407A (en) 1961-05-09
US3206468A (en) 1963-11-15 1965-09-14 Merck & Co Inc Methods of preparing benzimidazoles
US3178447A (en) 1964-05-05 1965-04-13 California Research Corp N-polyhaloalkylthio compounds
DE1209799B (en) 1964-05-14 1966-01-27 Bayer Ag Seed dressing against fusariosis
GB1094567A (en) 1964-06-23 1967-12-13 Zh Biseibutsu Kagaku Kenkyukai Plant disease protective and curative compositions
US3279610A (en) * 1964-07-27 1966-10-18 Gen Filter Co Water-treating apparatus
GB1114155A (en) 1964-08-24 1968-05-15 Evans Medical Ltd Guanidino derivatives
US3249499A (en) 1965-04-26 1966-05-03 Us Rubber Co Control of plant diseases
CH485776A (en) 1965-08-26 1970-02-15 Bayer Ag Process for the preparation of dithiolphosphoric acid triesters
GB1103989A (en) 1967-02-10 1968-02-21 Union Carbide Corp Fungicidal concentrates
NL157191C (en) 1966-12-17 Schering Ag PROCEDURE FOR PREPARING A PREPARATION WITH FUNGICIDE AND FUNGISTATIC ACTION.
US3629428A (en) 1967-09-07 1971-12-21 Meiji Seika Kaisha Pesticide for controlling bacterial and fungal diseases of rice plant
US3745187A (en) 1967-10-30 1973-07-10 Nippon Soda Co Bis-thioureido-benzenes and preparation thereof
US3745170A (en) 1969-03-19 1973-07-10 Sumitomo Chemical Co Novel n-(3,5-dihalophenyl)-imide compounds
US3631176A (en) 1970-07-20 1971-12-28 Du Pont Carbamoyl substituted 2-aminobenzimidazoles
FR2148868A6 (en) 1970-10-06 1973-03-23 Rhone Poulenc Sa
JPS5117536B2 (en) 1971-02-02 1976-06-03
US3912752A (en) 1972-01-11 1975-10-14 Bayer Ag 1-Substituted-1,2,4-triazoles
DE2207576C2 (en) 1972-02-18 1985-07-25 Basf Ag, 6700 Ludwigshafen Oxazolidine derivatives
DE2324010C3 (en) 1973-05-12 1981-10-08 Bayer Ag, 5090 Leverkusen 1-Substituted 2-triazolyl-2-phenoxyethanol compounds, process for their preparation and their use for combating fungi
GB1469772A (en) 1973-06-21 1977-04-06 Boots Co Ltd Fungicidal imidazole derivatives
US4046911A (en) 1974-04-02 1977-09-06 Ciba-Geigy Corporation N-(substituted phenyl)-n-furanoyl-alanine methyl esters and their use in fungicidal composition and methods
US4079062A (en) 1974-11-18 1978-03-14 Janssen Pharmaceutica N.V. Triazole derivatives
DE2543279A1 (en) 1975-09-27 1977-04-07 Basf Ag PROCESS FOR THE PREPARATION OF N-SUBSTITUTED TETRAHYDRO-1.4-OXAZINES
JPS5312844A (en) 1976-07-20 1978-02-04 Nippon Tokushu Noyaku Seizo Kk Nn44halogenobenzyllnnmethyl*or nonsubstitutedd*cycloalkylln**phenylurea or thiourea compounds* their preparation and fungicides containing the same as active constituents
JPS5329934A (en) * 1976-08-31 1978-03-20 Ihara Chem Ind Co Ltd Fungicides for agricultural and horticultural use
DE2656747C2 (en) 1976-12-15 1984-07-05 Basf Ag, 6700 Ludwigshafen Morpholine derivatives
US4598085A (en) 1977-04-27 1986-07-01 Janssen Pharmaceutica N.V. Fungicidal 1-(2-aryl-2-R-ethyl)-1H-1,2,4-triazoles
DE2802488A1 (en) 1978-01-20 1979-07-26 Bayer Ag 3-AZOLYL-BENZOTRIAZINE AND -BENZOTRIAZINE-1-OXIDES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING PLANT DISEASES
BG28977A3 (en) 1978-02-02 1980-08-15 Montedison Spa Fungicide means and method for fungus fighting
US4551469A (en) 1979-03-07 1985-11-05 Imperial Chemical Industries Plc Antifungal triazole ethanol derivatives
US4272417A (en) 1979-05-22 1981-06-09 Cargill, Incorporated Stable protective seed coating
US4245432A (en) 1979-07-25 1981-01-20 Eastman Kodak Company Seed coatings
AU542623B2 (en) * 1980-05-16 1985-02-28 Bayer Aktiengesellschaft 1-hydroxyethyl-azole derivatives
US4432989A (en) 1980-07-18 1984-02-21 Sandoz, Inc. αAryl-1H-imidazole-1-ethanols
DE3030026A1 (en) 1980-08-08 1981-03-26 Sandoz-Patent-GmbH, 79539 Lörrach Fungicidal 3-acylamino-oxazolidinone derivs. - prepd. by cyclisation of 2-haloethyl 2-acyl-2-phenyl-hydrazine carboxylate cpds.
US5266585A (en) 1981-05-12 1993-11-30 Ciba-Geigy Corporation Arylphenyl ether derivatives, compositions containing these compounds and use thereof
US4496551A (en) 1981-06-24 1985-01-29 E. I. Du Pont De Nemours And Company Fungicidal imidazole derivatives
CH658654A5 (en) 1983-03-04 1986-11-28 Sandoz Ag AZOLE DERIVATIVES, METHOD FOR THEIR PRODUCTION AND MEANS THAT CONTAIN THESE COMPOUNDS.
US4920139A (en) 1983-11-10 1990-04-24 Rohm And Haas Company Alpha-alkyl-alpha-(4-halophenyl)-1H-1,2,4-triazole-1-propanenitrile
JPS60178801A (en) 1984-02-24 1985-09-12 Dainippon Ink & Chem Inc Guanidine fungicide for agriculture and horticulture
WO1987003591A1 (en) 1985-12-12 1987-06-18 Ube Industries, Ltd. Novel imidazole derivatives, bactericides containing them, and process for their preparation
GB8429739D0 (en) 1984-11-24 1985-01-03 Fbc Ltd Fungicides
DE3511411A1 (en) 1985-03-29 1986-10-02 Basf Ag, 6700 Ludwigshafen USE OF AZOLYLMETHYLOXIRANES TO COMBAT VIRAL DISEASES
IT1204773B (en) 1986-01-23 1989-03-10 Montedison Spa FUNGICIDAL AZOLYL DERIVATIVES
EP0236272B1 (en) 1986-03-04 1991-06-12 Ciba-Geigy Ag Fungicidal use of a cyanopyrrole derivative
US5087635A (en) 1986-07-02 1992-02-11 Rohm And Haas Company Alpha-aryl-alpha-phenylethyl-1H-1,2,4-triazole-1-propanenitriles
DE256503T1 (en) 1986-08-12 1990-02-08 Mitsubishi Kasei Corp., Tokio/Tokyo PYRIDINE CARBOXAMIDE DERIVATIVES AND THEIR USE AS A FUNGICIDAL AGENT.
FR2603039B1 (en) 1986-08-22 1990-01-05 Rhone Poulenc Agrochimie 2,5-DIHYDROFURAN DERIVATIVES HAVING TRIAZOLE OR IMIDAZOLE GROUP, PROCESS FOR PREPARATION, USE AS FUNGICIDE
DE3783415D1 (en) 1986-08-29 1993-02-18 Shell Int Research ARYLOXYCARBONIC ACID DERIVATIVES, THEIR PRODUCTION AND USE.
EP0278595B2 (en) 1987-02-09 2000-01-12 Zeneca Limited Fungicides
US4808430A (en) 1987-02-27 1989-02-28 Yazaki Corporation Method of applying gel coating to plant seeds
DE3735555A1 (en) 1987-03-07 1988-09-15 Bayer Ag AMINOMETHYLHETEROCYCLEN
CA1339133C (en) 1987-03-13 1997-07-29 Rikuo Nasu Imidazole compounds and biocidal composition comprising the same for controlling harmful organisms
DE19775050I2 (en) 1987-08-21 2010-12-16 Syngenta Participations Ag Benzothiadiazoles and their use in processes and agents for plant diseases.
US5153200A (en) * 1987-09-28 1992-10-06 Ciba-Geigy Corporation Pesticides
ES2054867T3 (en) 1987-09-28 1994-08-16 Ciba Geigy Ag PESTICIDES AND PESTICIDES.
US4877441A (en) 1987-11-06 1989-10-31 Sumitomo Chemical Company Ltd. Fungicidal substituted carboxylic acid derivatives
IL89029A (en) 1988-01-29 1993-01-31 Lilly Co Eli Fungicidal quinoline and cinnoline derivatives, compositions containing them, and fungicidal methods of using them
JPH0762001B2 (en) 1988-02-16 1995-07-05 呉羽化学工業株式会社 Process for producing azolylmethylcycloalkanol derivative
DE3814505A1 (en) 1988-04-29 1989-11-09 Bayer Ag SUBSTITUTED CYCLOALKYL OR HETEROCYCLYL-CARBONIC ACID ANILIDE
DE3815728A1 (en) 1988-05-07 1989-11-16 Bayer Ag STEREOISOMERS OF N- (R) - (1-ARYL-ETHYL) -1-ALKYL-2,2-DICHLORO-CYCLOPROPANCARBONIC ACID AMIDES
US5256683A (en) 1988-12-29 1993-10-26 Rhone-Poulenc Agrochimie Fungicidal compositions containing (benzylidene)-azolylmethylcycloalkane
US5145856A (en) 1989-02-10 1992-09-08 Imperial Chemical Industries Plc Fungicides
UA35548C2 (en) 1989-04-21 2001-04-16 Е.І. Дюпон Де Немур Енд Компані oxazolidinone Derivatives, a process for the preparation thereof and FUNGICIDal COMPOSITION
DK0398692T3 (en) 1989-05-17 1996-09-16 Shionogi & Co Alkoxyiminoacetamide derivatives and their use as fungicides
PH11991042549B1 (en) 1990-06-05 2000-12-04
US5453531A (en) 1990-08-25 1995-09-26 Bayer Aktiengesellschaft Substituted valinamide derivatives
ES2088572T5 (en) 1991-01-30 2001-01-01 Zeneca Ltd FUNGICIDES
DE4117371A1 (en) 1991-05-28 1992-12-03 Basf Ag ANTIMYCOTIC AGENTS CONTAINING PHENYL ACIDSEED DERIVATIVES
US5306712A (en) 1991-10-09 1994-04-26 Sanyo Company, Limited Fungicidal silicon-containing compounds and their agrochemical and medicinal uses
US6002016A (en) 1991-12-20 1999-12-14 Rhone-Poulenc Agrochimie Fungicidal 2-imidazolin-5-ones and 2-imidazoline-5-thiones
US5593996A (en) 1991-12-30 1997-01-14 American Cyanamid Company Triazolopyrimidine derivatives
JPH0682723A (en) * 1992-09-01 1994-03-25 Hitachi Ltd Projection type television device
JP2783130B2 (en) 1992-10-02 1998-08-06 三菱化学株式会社 Methoxyiminoacetic acid derivatives and agricultural and horticultural fungicides containing the same as active ingredients
US5304572A (en) 1992-12-01 1994-04-19 Rohm And Haas Company N-acetonylbenzamides and their use as fungicides
US5254584A (en) 1992-12-18 1993-10-19 Rohm And Haas Company N-acetonylbenzamides and their use as fungicides
CN1050355C (en) 1993-05-12 2000-03-15 纳幕尔杜邦公司 Fungicidal fused bicyclic pyrimidinones
ZW8594A1 (en) 1993-08-11 1994-10-12 Bayer Ag Substituted azadioxacycbalkenes
US5514643A (en) 1993-08-16 1996-05-07 Lucky Ltd. 2-aminothiazolecarboxamide derivatives, processes for preparing the same and use thereof for controlling phytopathogenic organisms
DE4423612A1 (en) 1994-07-06 1996-01-11 Basf Ag 2 - [(Dihydro) pyrazolyl-3'-oxymethylene] anilides, process for their preparation and their use
DE4426753A1 (en) 1994-07-28 1996-02-01 Bayer Ag Means for controlling plant pests
RO118074B1 (en) 1994-08-03 2003-01-30 Kumiai Chemical Industry Co Amino acid amide derivatives, processes for preparing the same, fungicidal composition for agricultural or horticultural use and method for controlling fungi
DE19528046A1 (en) 1994-11-21 1996-05-23 Bayer Ag New sulphur substd tri:azole derivs
US5486621A (en) 1994-12-15 1996-01-23 Monsanto Company Fungicides for the control of take-all disease of plants
US5578725A (en) 1995-01-30 1996-11-26 Regents Of The University Of Minnesota Delta opioid receptor antagonists
JP3164762B2 (en) * 1995-04-11 2001-05-08 三井化学株式会社 Substituted thiophene derivatives and fungicides for agricultural and horticultural use containing the same as active ingredients
DE69618370T2 (en) * 1995-04-11 2002-09-26 Mitsui Chemicals, Inc. Substituted thiophene derivatives and fungicides containing them as an active ingredient for agriculture and horticulture
MY115814A (en) 1995-06-16 2003-09-30 Bayer Ip Gmbh Crop protection compositions
HUP9802822A3 (en) * 1995-08-10 1999-04-28 Bayer Ag Halobenzimidazol derivatives, intermediates, preparation thereof and microbocide compositions containing these compounds as active ingredients
DE19539324A1 (en) 1995-10-23 1997-04-24 Basf Ag Phenylacetic acid derivatives, processes and intermediates for their preparation and compositions containing them
DE19602095A1 (en) 1996-01-22 1997-07-24 Bayer Ag Halopyrimidines
US5876739A (en) 1996-06-13 1999-03-02 Novartis Ag Insecticidal seed coating
DE19646407A1 (en) 1996-11-11 1998-05-14 Bayer Ag Halopyrimidines
DE19716257A1 (en) 1997-04-18 1998-10-22 Bayer Ag Fungicidal active ingredient combination
US5945567A (en) 1997-08-20 1999-08-31 American Cyanamid Company Fungicidal 2-methoxybenzophenones
GB9719411D0 (en) 1997-09-12 1997-11-12 Ciba Geigy Ag New Pesticides
DE19750012A1 (en) 1997-11-12 1999-05-20 Bayer Ag Isothiazole carboxamides
JP3818771B2 (en) * 1998-02-12 2006-09-06 三井化学株式会社 Plant disease control composition
TW575562B (en) 1998-02-19 2004-02-11 Agrevo Uk Ltd Fungicides
JP3856561B2 (en) * 1998-04-15 2006-12-13 三井化学株式会社 Plant disease control composition
JP3824421B2 (en) * 1998-04-24 2006-09-20 三井化学株式会社 Plant disease control composition
JP3963569B2 (en) * 1998-04-24 2007-08-22 三井化学株式会社 Plant disease control composition
JP3963570B2 (en) * 1998-04-24 2007-08-22 三井化学株式会社 Plant disease control composition
JP3824420B2 (en) * 1998-04-24 2006-09-20 三井化学株式会社 Plant disease control composition
US5986135A (en) 1998-09-25 1999-11-16 American Cyanamid Company Fungicidal trifluoromethylalkylamino-triazolopyrimidines
US6503904B2 (en) 1998-11-16 2003-01-07 Syngenta Crop Protection, Inc. Pesticidal composition for seed treatment
JP4090639B2 (en) * 1999-09-03 2008-05-28 三井化学株式会社 Plant disease control composition
JP4112756B2 (en) * 1999-09-03 2008-07-02 三井化学株式会社 Plant disease control composition
JP4090638B2 (en) * 1999-09-03 2008-05-28 三井化学株式会社 Plant disease control composition
GB0011944D0 (en) 2000-05-17 2000-07-05 Novartis Ag Organic compounds
US6838473B2 (en) 2000-10-06 2005-01-04 Monsanto Technology Llc Seed treatment with combinations of pyrethrins/pyrethroids and clothiandin
JP2004513170A (en) 2000-11-13 2004-04-30 ビーエーエスエフ　アクチェンゲゼルシャフト 7- (R) -aminotriazolopyrimidines, their production and their use for controlling phytopathogenic fungi
US20020134012A1 (en) 2001-03-21 2002-09-26 Monsanto Technology, L.L.C. Method of controlling the release of agricultural active ingredients from treated plant seeds
DE10124208A1 (en) 2001-05-18 2002-11-21 Bayer Ag Use of triazolopyrimidine derivatives for protecting technical materials, particularly wood, paints and plastics, against microbes, particularly fungi
US6616054B1 (en) 2001-07-02 2003-09-09 Bellsouth Intellectual Property Corporation External power supply system, apparatus and method for smart card
FR2828196A1 (en) 2001-08-03 2003-02-07 Aventis Cropscience Sa New iodochromone derivatives, useful for the prevention or cure of plant fungal disorders, especially in cereals, vines, fruits, legumes or ornamental plants
JP4477358B2 (en) 2002-03-01 2010-06-09 ビーエーエスエフ ソシエタス・ヨーロピア Fungicidal mixtures based on prothioconazole and strobilurin derivatives
DE10228102A1 (en) 2002-06-24 2004-01-15 Bayer Cropscience Ag Fungicidal active ingredient combinations
DE102004029972A1 (en) * 2004-06-21 2006-01-05 Bayer Cropscience Ag Mordant for combating phytopathogenic fungi
PT1796465E (en) * 2004-09-27 2008-10-22 Du Pont Fungicidal mixtures of thiophene derivative
DE102004049761A1 (en) 2004-10-12 2006-04-13 Bayer Cropscience Ag Fungicidal drug combinations
NZ560376A (en) 2005-02-04 2010-03-26 Mitsui Chemicals Inc Plant pathogen control composition and method
DE102005035300A1 (en) 2005-07-28 2007-02-01 Bayer Cropscience Ag Synergistic fungicidal composition containing a carboxamide, azole and optionally strobilurin, for control of e.g. Puccinia or Erysiphe by treatment of plants, seeds or soil
WO2010139410A2 (en) 2009-06-02 2010-12-09 Bayer Cropscience Ag Use of succinate dehydrogenase inhibitors for controlling sclerotinia ssp.

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2006105888A2 *

Also Published As

Publication number Publication date
JP2008537945A (en) 2008-10-02
MX2007012289A (en) 2007-10-16
KR101333550B1 (en) 2013-11-28
KR20070118178A (en) 2007-12-13
JP5101491B2 (en) 2012-12-19
CA2843173A1 (en) 2006-10-12
UA91854C2 (en) 2010-09-10
CN101184391A (en) 2008-05-21
CN101184391B (en) 2013-07-24
CA2843176A1 (en) 2006-10-12
DE102005015677A1 (en) 2006-10-12
US20130281500A1 (en) 2013-10-24
US8575064B2 (en) 2013-11-05
US20130274099A1 (en) 2013-10-17
BRPI0607018A2 (en) 2009-08-04
US20100273648A1 (en) 2010-10-28
WO2006105888A3 (en) 2007-03-15
US20130281496A1 (en) 2013-10-24
WO2006105888A2 (en) 2006-10-12
EA200702174A1 (en) 2008-04-28
EA014663B1 (en) 2010-12-30
US20130274100A1 (en) 2013-10-17
CN102907432A (en) 2013-02-06
CA2603223A1 (en) 2006-10-12
US20130274101A1 (en) 2013-10-17
US20130281292A1 (en) 2013-10-24

Similar Documents

Publication Publication Date Title
EP2255649B1 (en) Agent combinations
EP1871167A2 (en) Synergistic fungicidal active substance combinations
EP2255658A1 (en) Agent combinations
EP2001299A2 (en) Fungicidal active substance combinations
WO2007104437A1 (en) Fungicidal active ingredient combinations
DE102006014723A1 (en) Fungicide combinations useful for plant and material protection comprise a pyrazole carboxamide and at least one fungicide selected from 24 groups of compounds
DE102006013784A1 (en) Fungicidal active combination used to combat phytopathogenic fungus, comprises carboxamide compound and e.g. strobilurin- or triazole- compound

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20071106

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20100607

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: BAYER INTELLECTUAL PROPERTY GMBH

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN

18W Application withdrawn

Effective date: 20150128