Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases

10.1021/acscatal.6b00504

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Main Authors: Sung, S, Sale, D, Braddock, D.C, Armstrong, A, Brennan, C, Davies, R.P
Other Authors: DEPT OF CHEMISTRY
Format: Article
Published: American Chemical Society 2020
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/183870
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spelling sg-nus-scholar.10635-1838702020-12-04T10:00:27Z Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases Sung, S Sale, D Braddock, D.C Armstrong, A Brennan, C Davies, R.P DEPT OF CHEMISTRY Amination Amines Catalysis Catalyst deactivation Catalysts Chemical reactions Copper Kinetic theory Kinetics Ligands Mass transfer Metal halides Reaction rates Activation mechanisms Bond coupling Concentration ranges First order kinetics Mass transfer effects Organic basis RPKA Ullmann reaction Reaction kinetics 10.1021/acscatal.6b00504 ACS Catalysis 6 6 3965-3974 2020-11-23T08:52:58Z 2020-11-23T08:52:58Z 2016 Article Sung, S, Sale, D, Braddock, D.C, Armstrong, A, Brennan, C, Davies, R.P (2016). Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases. ACS Catalysis 6 (6) : 3965-3974. ScholarBank@NUS Repository. https://doi.org/10.1021/acscatal.6b00504 2155-5435 https://scholarbank.nus.edu.sg/handle/10635/183870 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ American Chemical Society Unpaywall 20201031
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic Amination
Amines
Catalysis
Catalyst deactivation
Catalysts
Chemical reactions
Copper
Kinetic theory
Kinetics
Ligands
Mass transfer
Metal halides
Reaction rates
Activation mechanisms
Bond coupling
Concentration ranges
First order kinetics
Mass transfer effects
Organic basis
RPKA
Ullmann reaction
Reaction kinetics
spellingShingle Amination
Amines
Catalysis
Catalyst deactivation
Catalysts
Chemical reactions
Copper
Kinetic theory
Kinetics
Ligands
Mass transfer
Metal halides
Reaction rates
Activation mechanisms
Bond coupling
Concentration ranges
First order kinetics
Mass transfer effects
Organic basis
RPKA
Ullmann reaction
Reaction kinetics
Sung, S
Sale, D
Braddock, D.C
Armstrong, A
Brennan, C
Davies, R.P
Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases
description 10.1021/acscatal.6b00504
author2 DEPT OF CHEMISTRY
author_facet DEPT OF CHEMISTRY
Sung, S
Sale, D
Braddock, D.C
Armstrong, A
Brennan, C
Davies, R.P
format Article
author Sung, S
Sale, D
Braddock, D.C
Armstrong, A
Brennan, C
Davies, R.P
author_sort Sung, S
title Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases
title_short Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases
title_full Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases
title_fullStr Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases
title_full_unstemmed Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases
title_sort mechanistic studies on the copper-catalyzed n-arylation of alkylamines promoted by organic soluble ionic bases
publisher American Chemical Society
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/183870
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