Wu et al., 2008 - Google Patents
Immobilization of copper (II) in organic-inorganic hybrid materials: A highly efficient and reusable catalyst for the classic Ullmann reactionWu et al., 2008
- Document ID
- 6307878348464475045
- Author
- Wu Q
- Wang L
- Publication year
- Publication venue
- Synthesis
External Links
Snippet
The immobilization of copper (II) in organic-inorganic (silica gel) hybrid materials as catalysis for the homocoupling of aryl halides (classic Ullmann reaction) has been described. The homocoupling of aryl iodides, bromides and chlorides underwent smoothly …
- JPVYNHNXODAKFH-UHFFFAOYSA-N cu2+ data:image/svg+xml;base64,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 data:image/svg+xml;base64,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 [Cu+2] 0 title abstract description 46
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with heteroatoms or with carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B61/00—Other general methods
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Gao et al. | An enantioselective oxidative C–H/C–H cross-coupling reaction: highly efficient method to prepare planar chiral ferrocenes | |
Oi et al. | Nitrogen-directed ortho-arylation and-heteroarylation of aromatic rings catalyzed by ruthenium complexes | |
Kikelj | Recent progress in diaryl ether synthesis | |
Li et al. | A highly efficient three-component coupling of aldehyde, terminal alkyne, and amine via C–H activation catalyzed by reusable immobilized copper in organic–inorganic hybrid materials under solvent-free reaction conditions | |
Li et al. | An Amine‐, Copper‐and Phosphine‐Free Sonogashira Coupling Reaction Catalyzed by Immobilization of Palladium in Organic–Inorganic Hybrid Materials | |
Tu et al. | A robust hydrophilic pyridine-bridged bis-benzimidazolylidene palladium pincer complex: Synthesis and its catalytic application towards Suzuki–Miyaura couplings in aqueous solvents | |
Jiang et al. | Ligand relay catalysis enables asymmetric migratory reductive acylation of olefins or alkyl halides | |
Jadhav et al. | A Merrifield resin supported Pd–NHC complex with a spacer (Pd–NHC@ SP–PS) for the Sonogashira coupling reaction under copper-and solvent-free conditions | |
Yeom et al. | Silver (I)-catalyzed direct route to isoquinoline-N-oxides | |
Wang et al. | Palladium-catalyzed reaction of arylboronic acids with aliphatic nitriles: Synthesis of alkyl aryl ketones and 2-arylbenzofurans | |
Rao et al. | C (sp2)− C (sp2) Coupling in Water: Palladium (II) Complexes of N‐Pincer Tetradentate Porphyrins as Effective Catalysts | |
Shi et al. | Cu-catalyzed decarboxylative coupling of propiolic acids with boronic acids | |
Manikandan et al. | Synthesis, spectral characterization and crystal structure of Ni (II) pyridoxal thiosemicarbazone complexes and their recyclable catalytic application in the nitroaldol (Henry) reaction in ionic liquid media | |
Wu et al. | Immobilization of copper (II) in organic-inorganic hybrid materials: A highly efficient and reusable catalyst for the classic Ullmann reaction | |
Liu et al. | Reusable and efficient Pd (OAc) 2/TBAB/PEG-400 system for Suzuki-Miyaura cross-coupling reaction under ligand-free conditions | |
Xu et al. | A atom-efficient cross-coupling reaction of aryl iodides with triarylbismuths catalyzed by immobilization of palladium (II)-Schiff base complex in MCM-41 | |
Huang et al. | Copper-Catalyzed Si–H Bond Insertion Reaction of N-Propargyl Ynamides with Hydrosilanes | |
Zhu et al. | Bis (cyclohexanone) oxalyldihydrazone/copper (II) oxide-a novel and efficient catalytic system for Ullmann-type CN coupling in pure water | |
Liu et al. | Chloramine Salt Mediated Oxidative Halogenation of Terminal Alkynes with KI or NaBr: Practical Synthesis of 1-Bromoalkynes and 1-Iodoalkynes | |
Zheng et al. | Copper-Catalyzed General and Selective α-C (sp3)–H Silylation of Amides via 1, 5-Hydrogen Atom Transfer | |
Qin et al. | Suzuki-Miyaura cross-coupling of arenediazonium salts with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium catalyst | |
Chrétien et al. | Evaluation of polymer-supported vinyltin reagents in the Stille cross-coupling reaction | |
Chen et al. | Self-supported thiourea-palladium complexes: highly air-stable and recyclable catalysts for the Suzuki reaction in neat water | |
EP3227018B1 (en) | Chelation directed c-h activation reactions catalyzed by solid-supported palladium(ii) catalysts | |
Peng et al. | Ligand-free copper-catalyzed arylation of olefins by the Mizoroki-Heck reaction |