A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides
about
Exhibition of the Brønsted acid-base character of a Schiff base in palladium(II) complex formation: lithium complexation, fluxional properties and catalysis of Suzuki reactions in water.'Click' generated 1,2,3-triazole based organosulfur/selenium ligands and their Pd(ii) and Ru(ii) complexes: their synthesis, structure and catalytic applications.Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.Regio- and Stereospecific 1,3-Allyl Group Transfer Triggered by a Copper-Catalyzed Borylation/ortho-Cyanation Cascade.Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts.Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: synthesis of (-)-flustramine B.Regio- and chemoselective metalation of arenes and heteroarenes using hindered metal amide bases.Keggin type mono Ni(II)-substituted phosphomolybdate: a sustainable, homogeneous and reusable catalyst for Suzuki-Miyaura cross-coupling.Phosphorus-nitrogen-phosphorus ligands: cooperative effects between nitrogen and phosphorus substituents on catalytic activity.A simple and highly efficient P,O-type ligand for Suzuki-Miyaura cross-coupling of aryl halides.Organosulphur and related ligands in Suzuki-Miyaura C-C coupling.1-phosphabarrelene complexes of palladium and their use in Suzuki-Miyaura coupling reactions.When are tricoordinated PdII species accessible? Stability trends and mechanistic consequences.Phosphane-functionalized cycloheptatrienyl-cyclopentadienyl titanium sandwich complexes: phosphorus ligands with an integrated reducing agent for palladium(0) catalyst generation.Bis(2-diphenylphosphinoxynaphthalen-1-yl)methane: transition metal chemistry, Suzuki cross-coupling reactions and homogeneous hydrogenation of olefins.A Sterically Constrained Tricyclic PC3 Phosphine: Coordination Behavior and Insertion of Chalcogen Atoms into P-C Bonds.A highly efficient Friedel-Crafts reaction of 3-hydroxyoxindoles and aromatic compounds to 3,3-diaryl and 3-alkyl-3-aryloxindoles catalyzed by Hg(ClO4)2·3H2O.Copper(i) chloride promoted Csp(2)-N cross-coupling of 1,2-di(pyrimidin-2-yl) disulfides with amines: an efficient approach to obtain C2-amino functionalized pyrimidines.Catalytic Double Carbon-Boron Bond Formation for the Synthesis of Cyclic Diarylborinic Acids as Versatile Building Blocks for π-Extended Heteroarenes.Rapid Synthesis of D-A'-π-A Dyes through a One-Pot Three-Component Suzuki-Miyaura Coupling and an Evaluation of their Photovoltaic Properties for Use in Dye-Sensitized Solar Cells.A General Palladium-Catalyzed Hiyama Cross-Coupling Reaction of Aryl and Heteroaryl Chlorides.C-Cl bond activation and catalytic hydrodechlorination of hexachlorobenzene by cobalt and nickel complexes with sodium formate as a reducing agent.
P2860
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P2860
A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides
description
1999 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artikull shkencor
@sq
artículu científicu espublizáu en 1999
@ast
scientific article (publication date: 16 August 1999)
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 1999
@uk
مقالة علمية (نشرت في 16-8-1999)
@ar
name
A Highly Active Catalyst for t ...... uki Coupling of Aryl Chlorides
@ast
A Highly Active Catalyst for t ...... uki Coupling of Aryl Chlorides
@en
type
label
A Highly Active Catalyst for t ...... uki Coupling of Aryl Chlorides
@ast
A Highly Active Catalyst for t ...... uki Coupling of Aryl Chlorides
@en
prefLabel
A Highly Active Catalyst for t ...... uki Coupling of Aryl Chlorides
@ast
A Highly Active Catalyst for t ...... uki Coupling of Aryl Chlorides
@en
P1476
A Highly Active Catalyst for t ...... uki Coupling of Aryl Chlorides
@en
P2093
Buchwald SL
P304
P356
10.1002/(SICI)1521-3773(19990816)38:16<2413::AID-ANIE2413>3.0.CO;2-H
P577
1999-08-01T00:00:00Z