Cheung et al., 2011 - Google Patents
Base-Promoted Selective Aryl C–Br and C–I Bond Cleavage by Iridium (III) Porphyrin: Reduction of IrIII–OH to IrII for Metalloradical Ipso Substitution of Aryl–Halogen …Cheung et al., 2011
- Document ID
- 8995262723574223216
- Author
- Cheung C
- Chan K
- Publication year
- Publication venue
- Organometallics
External Links
Snippet
Base-promoted selective aryl carbon–bromine and carbon–iodine bond (Ar–X, X= Br, I) cleavage by iridium (III) porphyrin carbonyl chloride (IrIII (ttp)(CO) Cl) was achieved in the presence of base (K2CO3, NaOH) to give iridium (III) porphyrin aryls (IrIII (ttp) Ar) …
- 238000006467 substitution reaction 0 title abstract description 34
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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/30—Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
-
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- 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
- 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
- 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
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Cheung et al. | Base-Promoted Selective Aryl C–Br and C–I Bond Cleavage by Iridium (III) Porphyrin: Reduction of IrIII–OH to IrII for Metalloradical Ipso Substitution of Aryl–Halogen Bonds | |
Lim et al. | C–N cross-coupling via photoexcitation of nickel–amine complexes | |
Meng et al. | Ligand-controlled regioselective hydrocarboxylation of styrenes with CO2 by combining visible light and nickel catalysis | |
Bernskoetter et al. | Kinetics and mechanism of iridium-catalyzed dehydrogenation of primary amines to nitriles | |
Pan et al. | Enones from acid fluorides and vinyl triflates by reductive nickel catalysis | |
Paul et al. | Photoredox-assisted reductive cross-coupling: mechanistic insight into catalytic aryl–alkyl cross-couplings | |
González-Sebastián et al. | Nickel-catalyzed hydrosilylation of CO2 in the presence of Et3B for the synthesis of formic acid and related formates | |
Neeve et al. | Diboron (4) compounds: from structural curiosity to synthetic workhorse | |
Zhang et al. | Comparison of arylboron-based nucleophiles in Ni-catalyzed Suzuki–Miyaura cross-coupling with aryl mesylates and sulfamates | |
Lee et al. | Reactivity of Iridium PCP Pincer Complexes toward CO and CO2. Crystal Structures of IrH (κ2-O2COH){C6H3-2, 6-(CH2PBu t 2) 2} and IrH (C (O) OH){C6H3-2, 6-(CH2PBu t 2) 2}⊙ H2O | |
Kinzhalov et al. | ADC-based palladium catalysts for aqueous Suzuki–Miyaura cross-coupling exhibit greater activity than the most advantageous catalytic systems | |
Ren et al. | A structure–activity study of Ni-catalyzed alkyl–alkyl Kumada coupling. Improved catalysts for coupling of secondary alkyl halides | |
Cole et al. | Bis (μ-oxo) dicopper (III) complexes of a homologous series of simple peralkylated 1, 2-diamines: Steric modulation of structure, stability, and reactivity | |
Mo et al. | Dinuclear iron complex-catalyzed cross-coupling of primary alkyl fluorides with aryl Grignard reagents | |
Leowanawat et al. | Trans-chloro (1-naphthyl) bis (triphenylphosphine) nickel (II)/PCy3 catalyzed cross-coupling of aryl and heteroaryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates at room temperature | |
de Boer et al. | Ruthenium PNN (O) Complexes: Cooperative Reactivity and Application as Catalysts for Acceptorless Dehydrogenative Coupling Reactions | |
Patra et al. | Hydrogen production from formic acid and formaldehyde over ruthenium catalysts in water | |
Johnson et al. | A combined experimental and computational study of unexpected C− F bond activation intermediates and selectivity in the reaction of pentafluorobenzene with a (PEt3) 2Ni synthon | |
Jayarathne et al. | Small molecule activation chemistry of Cu–Fe heterobimetallic complexes toward CS2 and N2O | |
Gary et al. | Participation of carbonyl oxygen in carbon–carboxylate bond-forming reductive elimination from palladium | |
Green et al. | Group 9 and 11 metal (I) gallyl complexes stabilized by N-heterocyclic carbene coordination: first structural characterization of Ga− M (M= Cu or Ag) bonds | |
Wu et al. | Synthesis, properties, and reactivity with carbon dioxide of (allyl) 2Ni (L) complexes | |
Anaby et al. | Study of precatalyst degradation leading to the discovery of a new Ru0 precatalyst for hydrogenation and dehydrogenation | |
Penafiel et al. | Preparation, hydrogen bonds, and catalytic activity in metal-promoted addition of arylboronic acids to enones of a rhodium complex containing an NHC ligand with an alcohol function | |
Pandey et al. | Sterically demanding phosphines with 2, 6-dibenzhydryl-4-methylphenyl core: Synthesis of RuII, PdII, and PtII Complexes, and structural and catalytic studies |