Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes
about
Pd- and Ni-catalyzed cross-coupling reactions in the synthesis of organic electronic materialsPreparation and Applications of Functionalized Organozinc Compounds35 years of palladium-catalyzed cross-coupling with Grignard reagents: how far have we come?Direct Carboxylation of Aryl Tosylates by CO2 Catalyzed by In situ-Generated Ni(0).Rational exploration of N-heterocyclic carbene (NHC) palladacycle diversity: a highly active and versatile precatalyst for Suzuki-Miyaura coupling reactions of deactivated aryl and alkyl substrates.Total synthesis of the protein phosphatase 2A inhibitor lactodehydrothyrsiferol.Advances in the synthesis of glycosidic macrolides: clavosolides A-D and cyanolide A.Advances in the field of π-conjugated 2,2':6',2"-terpyridines.Pd-catalyzed cross-coupling reactions of alkyl halides.Cross-coupling in flow.Synthesis of binaphthyl based phosphine and phosphite ligands.Polymers for electronics and spintronics.Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV.Metal-catalyzed activation of ethers via C-O bond cleavage: a new strategy for molecular diversity.Ni-Catalyzed C-C Couplings Using Alkyl Electrophiles.Oxidative addition of the C-I bond on aluminum nanoclusters.Palladium Catalyst Supported on Zeolite for Cross-coupling Reactions: An Overview of Recent Advances.Recent Progress in Application of Graphene Supported Metal Nanoparticles in C-C and C-X Coupling Reactions.A triazine-based Ni(II) PNP pincer complex as catalyst for Kumada-Corriu and Negishi cross-coupling reactions.On the radical nature of iron-catalyzed cross-coupling reactions.Direct heteroarylation polymerization: guidelines for defect-free conjugated polymers.Palladium- (and nickel-) catalyzed vinylation of aryl halides.Polythiophenes Comprising Conjugated Pendants for Polymer Solar Cells: A Review.Transition-metal-free one-pot synthesis of biaryls from Grignard reagents and substituted cyclohexanones.The AZARYPHOS family of ligands for ambifunctional catalysis: syntheses and use in ruthenium-catalyzed anti-Markovnikov hydration of terminal alkynes.Pd-catalyzed one-pot sequential unsymmetrical cross-coupling reactions of aryl/heteroaryl 1,2-dihalides.Association and Dissociation of Grignard Reagents RMgCl and Their Turbo Variant RMgCl⋅LiCl.Regioselective carbon-carbon bond formation in proteins with palladium catalysis; new protein chemistry by organometallic chemistry.Chemistry in Confinement: Copper and Palladium Catalyzed Ecofriendly Organic Transformations within Porous Frameworks.NI(ii) phosphine and phosphide complexes supported by a PNP-pyrrole pincer ligand.Fast, Efficient and Low E-Factor One-Pot Palladium-Catalyzed Cross-Coupling of (Hetero)Arenes.Pd-mediated cross-coupling of C-17 lithiated androst-16-en-3-ol - access to functionalized arylated steroid derivatives.The 2010 Chemistry Nobel Prize to R.F. Heck, E. Negishi, and A. Suzuki for palladium-catalyzed cross-coupling reactions.Palladium-catalyzed intramolecular reductive cross-coupling of Csp2-Csp3 bond formation.Nickel complexes incorporating an amido phosphine chelate with a pendant amine arm: synthesis, structure, and catalytic Kumada coupling.Nickel-catalyzed sp2 C-H bonds arylation of N-aromatic heterocycles with Grignard reagents at room temperature.Oxidant-free dehydrogenative coupling reactions via hydrogen evolution.Iridium(iii)-catalyzed regioselective direct arylation of sp(2) C-H bonds with diaryliodonium salts.Palladium-catalyzed cross-coupling of unactivated alkenes with acrylates: application to the synthesis of the C13-C21 fragment of palmerolide A.Kumada-Corriu reactions in a pressure-driven microflow reactor.
P2860
Q28822356-CD48BA6A-5326-47FB-8568-CA81253F303DQ29542165-8521F52D-231F-4D27-9854-34036F4FF1CEQ29999174-E0E078E7-53F2-4874-B3A1-D5F5EDFD4844Q33466432-5D48AFD8-AB2C-4F0D-891F-ECB0F8E94A63Q33533417-16F577DC-8DEC-4C32-9E0A-0DD51F2CF6A3Q35119931-83C7BB65-1B2E-4312-88A4-EE53466D923BQ36156057-B5630371-6CF6-4D28-B586-277A4B2AECCEQ37820904-D694D928-595E-495E-9BA8-250EBC318127Q37904753-C05137CB-BD28-4ED8-8CFF-9955EB059DD9Q37914019-61F8E202-CFDE-4903-A866-BED1DE92483FQ38115696-275A802C-4E82-4D7A-8418-64055FD1B64FQ38137004-B955F91B-E0C9-4BC5-A43D-BE1199C18F5FQ38206709-3CFB7B3C-30BF-46F3-911D-29D78C93B488Q38243353-FD7395FE-C4C9-4D0E-AEE6-9DAB03A4330EQ38942612-ACC2D4BA-7A3F-436D-A617-C28AE14A28AAQ38990051-F2ED29B7-43A3-4F9A-95D0-1C0F2DE5935BQ39032569-A58CDA7A-E672-4D7D-8A5A-218A9AAFC070Q39459154-0AA58020-44E6-4CDC-AE8A-F3B420AFC12EQ41186470-E8B11FB7-A5D4-49D9-A9C4-889A2001A1E2Q41374605-1D62BED3-44CA-41F7-BE1B-73C2BFF8A85FQ41664505-6FA71091-3BF1-4D98-AA2E-BE17CBE56B81Q41890738-4E8263F7-825E-4C1B-8602-FDCD448CC6AEQ42064533-4A8AD762-B739-4AAB-B02B-FB52ABAC09E5Q45015241-4669DB30-8362-499F-BE45-5B18A6C362E9Q45959258-3117C918-94F0-43D5-BD15-C641BFF5990EQ46109368-E10582BE-8729-4C6C-B93C-7154E8E0294DQ46552862-83B20567-179C-4CEE-8B42-1ED8F421F7DEQ46819695-36738DD6-46F6-49F0-80AE-74B38735CFD4Q47820099-5F636A7D-5BDB-4D6F-8111-A37C0333A83BQ48133969-FC7B8D59-7F11-4664-8B19-69457D85BD4BQ48167854-C73CBA7C-3E88-4549-BA31-9310711C93E0Q48194746-68BAC7EE-0730-4331-AE65-753C542E8830Q48303245-39C7FB03-3087-4012-B088-24F90DA23038Q50455391-E6F6E18F-805C-4DC5-A22D-15F5B58952B5Q50506964-CFA274A7-C901-4468-BB75-9D151A077409Q50512914-0BB5EF5F-2447-4FA8-9C92-A9CA2F946BD9Q51062141-68AF7D4C-DC57-48BE-816B-74FDEC3915A8Q51265861-0DA18292-EAFF-495D-9F17-711551105CB4Q51323542-3554E494-2EB1-4C8A-ADCC-FB3AF9591A12Q51597001-C7406FA3-610B-4D77-8AEA-AF0B3FC3EC85
P2860
Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes
description
article
@en
im Juni 1972 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 1972
@uk
ലേഖനം
@ml
name
Selective carbon-carbon bond f ...... by nickel-phosphine complexes
@en
Selective carbon-carbon bond f ...... by nickel-phosphine complexes
@nl
type
label
Selective carbon-carbon bond f ...... by nickel-phosphine complexes
@en
Selective carbon-carbon bond f ...... by nickel-phosphine complexes
@nl
prefLabel
Selective carbon-carbon bond f ...... by nickel-phosphine complexes
@en
Selective carbon-carbon bond f ...... by nickel-phosphine complexes
@nl
P2093
P356
P1476
Selective carbon-carbon bond f ...... by nickel-phosphine complexes
@en
P2093
Kohei Tamao
Koji Sumitani
Makoto Kumada
P304
P356
10.1021/JA00767A075
P407
P577
1972-06-01T00:00:00Z