Enantiopure enynyl sulfoxides via palladium-catalyzed coupling reactions

DOI: 10.1016/S0040-4039(00)79195-7

Source and publish data:

Tetrahedron Letters p. 3663 - 3666 (1993)

Update date:2022-08-05

Topics:

Authors:

Paley Paley

Lafontaine

Paz Ventura

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Article abstract of DOI:10.1016/S0040-4039(00)79195-7

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.

Full text of DOI:10.1016/S0040-4039(00)79195-7

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