Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases
10.1021/acscatal.6b00504
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2020
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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 |
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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 |
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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 |
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10.1021/acscatal.6b00504 |
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DEPT OF CHEMISTRY |
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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 |
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American Chemical Society |
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2020 |
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https://scholarbank.nus.edu.sg/handle/10635/183870 |
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1686109310733516800 |