Enantiopure Enynyl Sulfoxides Via Palladium-Catalyzed Coupling Reactions

Authors

Robert S. Paley, Swarthmore CollegeFollow
J. A. LafontaineFollow
M. P. Ventura

Document Type

Article

Publication Date

6-4-1993

Published In

Tetrahedron Letters

Abstract

Enantiomerically pure 1-sulfinyl-1-en-3-ynes are prepared from 2-halovinylsulfoxides via Sonogashira or Stille coupling procedures. The trans-enynyl sulfoxides may be hydrogenated to provide (1E, 3Z)-dienylsulfoxides.

Recommended Citation

Robert S. Paley, J. A. Lafontaine, and M. P. Ventura. (1993). "Enantiopure Enynyl Sulfoxides Via Palladium-Catalyzed Coupling Reactions". Tetrahedron Letters. Volume 34, Issue 23. 3663-3666. DOI: 10.1016/S0040-4039(00)79195-7
https://works.swarthmore.edu/fac-chemistry/61