A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
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Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation.Rh(I)-catalyzed direct arylation of azines.Palladium-catalyzed 1,1-difunctionalization of ethylene.Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts.Rh(I)-catalyzed direct arylation of pyridines and quinolines.Scope of the Suzuki-Miyaura cross-coupling reactions of potassium heteroaryltrifluoroborates.A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates.Synthesis of solid 2-pyridylzinc reagents and their application in Negishi reactionsRegio- and chemoselective metalation of arenes and heteroarenes using hindered metal amide bases.Transmetalation in the Suzuki-Miyaura coupling: the fork in the trail.Selection of boron reagents for Suzuki-Miyaura coupling.Catalytic C-H bond functionalisation of purine and pyrimidine nucleosides: a synthetic and mechanistic perspective.Pyridine sulfinates as general nucleophilic coupling partners in palladium-catalyzed cross-coupling reactions with aryl halides.Selective and Serial Suzuki-Miyaura Reactions of Polychlorinated Aromatics with Alkyl Pinacol Boronic Esters.Development of a palladium-catalyzed decarboxylative cross-coupling of (2-azaaryl)carboxylates with aryl halides.A general method for Suzuki-Miyaura coupling reactions using lithium triisopropyl borates.General method for synthesis of 2-heterocyclic N-methyliminodiacetic acid boronates.A general solution for the 2-pyridyl problem.Gold catalysis: in situ EXAFS study of homogeneous oxidative esterification.Four-component synthesis of fully substituted 1,2,4-triazoles.Arylation of 2-substituted pyridines via Pd-catalyzed decarboxylative cross-coupling reactions of 2-picolinic acid.A cyclopalladated complex of corannulene with a pyridine pendant and its columnar self-assembly.Self-liganded Suzuki-Miyaura coupling for site-selective protein PEGylation.Suzuki-Miyaura Cross-Coupling Reactions of Highly Fluorinated Arylboronic Esters: Catalytic Studies and Stoichiometric Model Reactions on the Transmetallation Step.Design, Synthesis, and Application of Polymer-Supported Silicon-Transfer Agents for Cross-Coupling Reactions with Organolithium Reagents.Efficient Ni-catalyzed conversion of phenols protected with 2,4,6-trichloro-1,3,5-triazine (TCT) to olefins.Pd(OAc)2 in WERSA: a novel green catalytic system for Suzuki-Miyaura cross-coupling reactions at room temperature.Direct arylation of N-heteroarenes with aryldiazonium salts by photoredox catalysis in water.Palladium-catalyzed direct C-H arylation of pyridine N-oxides with potassium aryl- and heteroaryltrifluoroborates.Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol esters.Copper-catalyzed direct C-H arylation of pyridine N-oxides with arylboronic esters: one-pot synthesis of 2-arylpyridines.
P2860
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P2860
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
@en
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles.
@nl
type
label
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
@en
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles.
@nl
prefLabel
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
@en
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles.
@nl
P2860
P356
P1476
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
@en
P2093
Kelvin L Billingsley
Stephen L Buchwald
P2860
P304
P356
10.1002/ANIE.200801465
P407
P577
2008-01-01T00:00:00Z