Suzuki-Miyaura cross-coupling reactions in aqueous media: green and sustainable syntheses of biaryls.
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Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides.Click with a boronic acid handle: a neighboring group-assisted click reaction that allows ready secondary functionalization.Cross-coupling in flow.Palladium-catalyzed modification of unprotected nucleosides, nucleotides, and oligonucleotides.Recent Progress in Application of Graphene Supported Metal Nanoparticles in C-C and C-X Coupling Reactions."Designer"-Surfactant-Enabled Cross-Couplings in Water at Room TemperatureOrganosulphur and related ligands in Suzuki-Miyaura C-C coupling.Expanded ring diaminocarbene palladium complexes: synthesis, structure, and Suzuki-Miyaura cross-coupling of heteroaryl chlorides in water.A general method of Suzuki-Miyaura cross-coupling of 4- and 5-halo-1,2,3-triazoles in water.Single and Twofold Metal- and Reagent-Free Anodic C-C Cross-Coupling of Phenols with Thiophenes.Pd(OAc)2 in WERSA: a novel green catalytic system for Suzuki-Miyaura cross-coupling reactions at room temperature.Pd-tetrahydrosalan-type complexes as catalysts for sonogashira couplings in water: efficient greening of the procedure.Fibrous nano-silica (KCC-1)-supported palladium catalyst: Suzuki coupling reactions under sustainable conditions.Suzuki-Miyaura cross-coupling coupling reactions with low catalyst loading: a green and sustainable protocol in pure water.Sonochemical synthesis of pyrido[2,3-d:6,5-d']-dipyrimidines catalyzed by [HNMP]+[HSO4]- and their antimicrobial activity studies.Water compatible multicomponent cascade Suzuki/Heck-aldol, Suzuki-aldol-Suzuki, and aldol-Suzuki-aldol reactions: an ecofriendly paradigm for multiple carbon-carbon bond formation in one pot.An enantioselective artificial Suzukiase based on the biotin-streptavidin technology.Highly Dispersed Palladium Nanoparticle-Loaded Magnetic Catalyst (FeS@EP–AG–Pd) for Suzuki Reaction in WaterSynthesis of novel allyl palladium complexes bearing purine based NHC and a water soluble phosphine and their catalytic activity in the Suzuki-Miyaura coupling in waterPalladium catalytic systems with hybrid pyrazole ligands in C–C coupling reactions. Nanoparticles versus molecular complexesWell-controlled synthesis of boronic-acid functionalised poly(lactide)s: a versatile platform for biocompatible polymer conjugates and sensorsHydrophilic Pd0Complexes Based on Sugars for Efficient Suzuki-Miyaura Coupling in Aqueous SystemsCross-Coupling Reactions in Aqueous MediaMetal-Catalyzed Cross-Couplings of Aryl Halides to Form C-C Bonds in Aqueous MediaCyclometalated iridium complexes for transfer hydrogenation of carbonyl groups in waterEfficient Suzuki⁻Miyaura C-C Cross-Couplings Induced by Novel Heterodinuclear Pd-bpydc-Ln ScaffoldsAdvances in carbon nanotubes as efficacious supports for palladium-catalysed carbon–carbon cross-coupling reactions
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Suzuki-Miyaura cross-coupling reactions in aqueous media: green and sustainable syntheses of biaryls.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Suzuki-Miyaura cross-coupling ...... tainable syntheses of biaryls.
@en
Suzuki-Miyaura cross-coupling ...... tainable syntheses of biaryls.
@nl
type
label
Suzuki-Miyaura cross-coupling ...... tainable syntheses of biaryls.
@en
Suzuki-Miyaura cross-coupling ...... tainable syntheses of biaryls.
@nl
prefLabel
Suzuki-Miyaura cross-coupling ...... tainable syntheses of biaryls.
@en
Suzuki-Miyaura cross-coupling ...... tainable syntheses of biaryls.
@nl
P356
P1433
P1476
Suzuki-Miyaura cross-coupling ...... tainable syntheses of biaryls.
@en
P2093
Audrey Decottignies
Aziz Fihri
P304
P356
10.1002/CSSC.200900221
P577
2010-05-01T00:00:00Z