153123-09-2Relevant articles and documents
Asymmetric chemical oxidations of aryl and alkyl 2-(trimethylsilyl)ethyl sulfides
Schwan,Pippert
, p. 131 - 138 (1995)
A collection of aryl and alkyl 2-(trimethylsilyl)methyl sulfides have been converted to their respective sulfoxides by four different asymmetric oxidizing agents. The chemical yields range from 44-98% while the enantiomeric excesses range from 0-89%. The
Convenient Preparation of Optically Pure Propargylic Alcohols Using 2-(Trimethylsilyl)vinyl Sulfoxide As A Novel Chiral Synthon
Kusuda, Shinya,Kawamura, Kiyoshi,Ueno, Yoshio,Toru, Takeshi
, p. 6587 - 6590 (2007/10/02)
Both enentiomers of optically pure propargylic alcohols are conveniently prepared by the reaction of α-vinyl anion of 2-(trimethylsilyl)vinyl p-tolyl sulfoxide with aldehydes and subsequent either desilylsulfination or thermal elimination of the sulfinyl group.