Reaction mechanisms of transition-metal-catalyzed azide–alkyne cycloaddition “click” reactions: A DFT investigation-Reference-Cited by-同舟云学术

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Reaction mechanisms of transition-metal-catalyzed azide–alkyne cycloaddition “click” reactions: A DFT investigation

Published:2015-12 Issue: Volume:1073 Page:131-138
ISSN:2210-271X
Container-title:Computational and Theoretical Chemistry
language:en
Short-container-title:Computational and Theoretical Chemistry

Author:

Ikhlef Djamila,Wang Changlong,Kahlal Samia,Maouche Boubekeur,Astruc Didier,Saillard Jean-Yves

Funder

Ministère de l’Enseignement Supérieur et de la Recherche Scientifique of Algeria

University of Bouira

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference50 articles.

1. Click chemistry: diverse chemical function from a few good reactions;Kolb;Angew. Chem. Int. Ed.,2001

2. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective “ligation” of azides and terminal alkynes;Rostovtsev;Angew. Chem. Int. Ed.,2002

3. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides;Tornøe;J. Org. Chem.,2002

4. 1,3-Dipolar cycloadditions;Huisgen;Angew. Chem. Int. Ed. Engl.,1963

5. Cu-catalyzed azide–alkyne cycloaddition;Meldal;Chem. Rev.,2008

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