articleEuropean Journal of Organic ChemistryOct 25, 2005Closed access

Cu I ‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective

University of Amsterdam

Indexed incrossref

Abstract

Abstract Cu I ‐catalyzed alkyne–azide cycloaddition provides 1,4‐disubstituted 1,2,3‐triazoles with such efficiency and scope that the transformation has been described as “click” chemistry. An overview of the mechanism of this remarkable reaction is presented as a means to explain the myriad of experimental results, particularly the various methods of catalyst generation, solvent and substrate effects, and choice of base or ligand. Both solution‐phase and solid‐phase results are comprehensively examined. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)

Citation impact

1,425
total citations
FWCI
59.41
Percentile
100%
References
108
Citations per year

Authors

3

Topics & keywords

Keywords
  • Cycloaddition
  • Chemistry
  • Alkyne
  • Azide
  • Click chemistry
  • Catalysis
  • Combinatorial chemistry
  • Ligand (biochemistry)
No related works found for this paper.