80401-23-6Relevant articles and documents
Radical, one-step approach to o-chlorophenyl thioethers from xanthates. A rapid access to vinylsilanes
Corbet, Matthieu,Ferjancic, Zorana,Quiclet-Sire, Beatrice,Zard, Samir Z.
supporting information; experimental part, p. 3579 - 3582 (2009/05/07)
(Chemical Equation Presented) Xanthates have been readily converted into o-chlorophenyl thioethers using a one-step procedure conducted under radical conditions. In some selected cases, these aryl thioethers were successfully oxidized to the corresponding sulfoxides and sulfenic acid elimination afforded the corresponding vinylsilanes.
SYNTHESIS OF VINYLSILANES BY PALLADIUM-CATALYZED REACTION OF TRIMETHYLSILYLALLYL ACETATES WITH NUCLEOPHILES
Hirao, Toshikazu,Enda, Jun,Ohshiro, Yoshiki,Agawa, Toshio
, p. 3079 - 3080 (2007/10/02)
Treatment of 1-trimethylsilylallyl and 3-trimethylsilylallyl acetates with nucleophiles (active methylene compounds and enamines) in the presence of a catalytic amount of Pd(PPh3)4 affords vinylsilane derivatives selectively.