Copper(I)-catalyzed cycloaddition of bismuth(III) acetylides with organic azides: synthesis of stable triazole anion equivalents

Angew Chem Int Ed Engl. 2013 Dec 2;52(49):13037-41. doi: 10.1002/anie.201306192. Epub 2013 Oct 15.

Abstract

Fully loaded: Readily accessible and shelf-stable 1-bismuth(III) acetylides react rapidly and regiospecifically with organic azides in the presence of a copper(I) catalyst. The reaction tolerates many functional groups and gives excellent yields of the previously unreported 5-bismuth triazolides. This uniquely reactive intermediate is functionalized under mild reaction conditions to give fully substituted 1,2,3-triazoles.

Keywords: bismuth; click chemistry; copper; cycloaddition; heterocycles.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Azides / chemistry*
  • Bismuth / chemistry*
  • Catalysis
  • Cations, Monovalent / chemistry
  • Copper / chemistry*
  • Cycloaddition Reaction
  • Organometallic Compounds / chemistry*
  • Triazoles / chemical synthesis*
  • Triazoles / chemistry

Substances

  • Azides
  • Cations, Monovalent
  • Organometallic Compounds
  • Triazoles
  • Copper
  • Bismuth