150764-17-3Relevant academic research and scientific papers
Enantiopure enynyl sulfoxides via palladium-catalyzed coupling reactions
Paley,Lafontaine,Paz Ventura
, p. 3663 - 3666 (1993)
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.
Synthesis and diastereoselective complexation of enantiopure sulfinyl dienes: The preparation of sulfinyl iron(0) dienes
Paley, Robert S.,De Dios, Alfonso,Estroff, Lara A.,Lafontaine, Jennifer A.,Montero, Carlos,McCulley, David J.,Rubio, M. Belen,Ventura, Maria Paz,Weers, Heather L.,De la Pradilla, Roberto Fernandez,Castro, Sonia,Dorado, Rocio,Morente, Miguel
, p. 6326 - 6343 (2007/10/03)
The preparation of a diverse array of enantiomerically pure 1- and 2- sulfinyl dienes has been achieved via Stille coupling of halovinyl sulfoxides and vinyl stannanes, hydrogenation of 1-sulfinyl-1-en-3-ynes, or vinylcupration of 1-sulfinyl alkynes. Form
