Suzuki-Miyaura cross-coupling of unprotected, nitrogen-rich heterocycles: substrate scope and mechanistic investigation.
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Mild Pd-catalyzed aminocarbonylation of (hetero)aryl bromides with a palladacycle precatalystRegioselective synthesis of benzimidazolones via cascade C-N coupling of monosubstituted ureas.Non-Directed Allylic C-H Acetoxylation in the Presence of Lewis Basic Heterocycles.Highly functionalized biaryls via Suzuki-Miyaura cross-coupling catalyzed by Pd@MOF under batch and continuous flow regimes.In-Depth Assessment of the Palladium-Catalyzed Fluorination of Five-Membered Heteroaryl Bromides.Suzuki-Miyaura cross-coupling optimization enabled by automated feedback.Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV.Ortho group activation of a bromopyrrole ester in Suzuki-Miyaura cross-coupling reactions: Application to the synthesis of new microtubule depolymerizing agents with potent cytotoxic activities.Living GenoChemetics by hyphenating synthetic biology and synthetic chemistry in vivoSynthesis of Indole-2-carboxylate Derivatives via Palladium-Catalyzed Aerobic Amination of Aryl C-H Bonds.Late-Stage Diversification of Biologically Active Molecules via Chemoenzymatic C-H Functionalization.Chemistry informer libraries: a chemoinformatics enabled approach to evaluate and advance synthetic methods.HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature.Metal-free nitroxyl radical-mediated β-C(sp3)-H amination of saturated ketones with heteroaryl halides: multiple roles of TEMPO.Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.Synthesis of 4-substituted pyrazole-3,5-diamines via Suzuki-Miyaura coupling and iron-catalyzed reduction.CO2-promoted oxidative cross-coupling reaction for C-S bond formation via masked strategy in an odourless way.Alkali metal mediated C-C bond coupling reaction.Suzuki-Type Cross-Coupling Reaction of Unprotected 3-Iodoindazoles with Pinacol Vinyl Boronate: An Expeditive C-3 Vinylation of Indazoles under Microwave Irradiation
P2860
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P2860
Suzuki-Miyaura cross-coupling of unprotected, nitrogen-rich heterocycles: substrate scope and mechanistic investigation.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 16 August 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Suzuki-Miyaura cross-coupling ...... and mechanistic investigation.
@en
Suzuki-Miyaura cross-coupling ...... and mechanistic investigation.
@nl
type
label
Suzuki-Miyaura cross-coupling ...... and mechanistic investigation.
@en
Suzuki-Miyaura cross-coupling ...... and mechanistic investigation.
@nl
prefLabel
Suzuki-Miyaura cross-coupling ...... and mechanistic investigation.
@en
Suzuki-Miyaura cross-coupling ...... and mechanistic investigation.
@nl
P2093
P2860
P356
P1476
Suzuki-Miyaura cross-coupling ...... and mechanistic investigation.
@en
P2093
Kelvin L Billingsley
M Alexander Düfert
Stephen L Buchwald
P2860
P304
12877-12885
P356
10.1021/JA4064469
P407
P577
2013-08-16T00:00:00Z