A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides.
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Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluoridesCatalysis for fluorination and trifluoromethylationPhotoredox Catalysis in Organic ChemistryPd-catalyzed N-arylation of secondary acyclic amides: catalyst development, scope, and computational studyPd-catalyzed cross-coupling reactions of amides and aryl mesylates.Gold-catalyzed cyclizations of cis-enediynes: insights into the nature of gold-aryne interactions.An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.Synthesis of heterocycles via Pd-ligand controlled cyclization of 2-chloro-N-(2-vinyl)aniline: preparation of carbazoles, indoles, dibenzazepines, and acridines.Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THFDialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chloridesA multiligand based Pd catalyst for C-N cross-coupling reactions.Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflatesNickel-catalyzed cross-couplings involving carbon-oxygen bondsSuzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.Palladium-catalyzed C,N-cross coupling reactions of 3-halo-2-aminopyridines.Pd-catalyzed conversion of aryl chlorides, triflates, and nonaflates to nitroaromaticsOrthogonal Cu- and Pd-based catalyst systems for the O- and N-arylation of aminophenols.Palladium-catalyzed amination of unprotected halo-7-azaindolesSimple, Efficient Protocols for the Pd-Catalyzed Cross-Coupling Reaction of Aryl Chlorides and Dimethylamine.Efficient Pd-catalyzed amination reactions for heterocycle functionalizationConcise palladium-catalyzed synthesis of dibenzodiazepines and structural analoguesRational ligand design for the arylation of hindered primary amines guided by reaction progress kinetic analysis.Aryloxyethyl Thiocyanates Are Potent Growth Inhibitors of Trypanosoma cruzi and Toxoplasma gondii.Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinibExperimental and computational evidence for gold vinylidenes: generation from terminal alkynes via a bifurcation pathway and facile C-H insertionsPalladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most CasesEvidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides.Nickel-catalyzed amination of aryl sulfamates.A bulky biaryl phosphine ligand allows for palladium-catalyzed amidation of five-membered heterocycles as electrophilesNickel-catalyzed amination of aryl sulfamates and carbamates using an air-stable precatalystA single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols.Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes.An Improved Synthesis of BrettPhos and RockPhos-Type Biarylphosphine Ligands.STILLE CROSS-COUPLING REACTIONS OF ARYL MESYLATES AND TOSYLATES USING A BIARYLPHOSPHINE BASED CATALYST SYSTEM.Aryl amination using ligand-free Ni(II) salts and photoredox catalysis.Design, synthesis and biological evaluation of WC-9 analogs as antiparasitic agentsSelective monoarylation of acetate esters and aryl methyl ketones using aryl chlorides.An efficient process for pd-catalyzed C-N cross-coupling reactions of aryl iodides: insight into controlling factors.A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates.
P2860
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P2860
A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 18 September 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
A highly active catalyst for P ...... y amines using aryl chlorides.
@en
A highly active catalyst for P ...... y amines using aryl chlorides.
@nl
type
label
A highly active catalyst for P ...... y amines using aryl chlorides.
@en
A highly active catalyst for P ...... y amines using aryl chlorides.
@nl
prefLabel
A highly active catalyst for P ...... y amines using aryl chlorides.
@en
A highly active catalyst for P ...... y amines using aryl chlorides.
@nl
P2093
P2860
P356
P1476
A highly active catalyst for P ...... y amines using aryl chlorides.
@en
P2093
Brett P Fors
Donald A Watson
Mark R Biscoe
Stephen L Buchwald
P2860
P304
13552-13554
P356
10.1021/JA8055358
P407
P577
2008-09-18T00:00:00Z