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Copper(I)-Catalyzed Cycloaddition of Bismuth(III) Acetylides with Organic Azides: Synthesis of Stable Triazole Anion Equivalents

Authors


  • This work was supported by the National Institute of General Medical Sciences, National Institutes of Health (GM-087620). Prof. Jason Hein (U.C. Merced), Dr. David Sarlah, and Will Gutekunst are gratefully acknowledged for helpful scientific discussions.

Abstract

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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 (see scheme). 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.

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