107006-49-5Relevant academic research and scientific papers
The synthesis of α-acetoxy sulfides and their Lewis acid-mediated reactions
Kraus, George A.
, p. 2599 - 2602 (2007/10/02)
α-Acetoxy sulfides can be conveniently prepared by the reaction of dithioacetals with mercuric acetate at ambient temperature. They react with allyltrimethylsilane, enol silyl ethers, and cyanotrimethylsilane in the presence of SnCl4 to afford
An Effective Activation of O-Trimethylsilyl Monothioacetal under Extremely Mild Conditions Using a Novel Catalyst System, Trimethylsilyl Chloride and Indium(III) Chloride
Mukaiyama, Teruaki,Ohno, Takashi,Nishimura, Takashi,Han, Jeong Sik,Kobayashi, Shu
, p. 2239 - 2242 (2007/10/02)
A novel catalyst system, trimethylsilyl chloride and indium(III) chloride, effectively catalyzes the reaction of O-trimethylsilyl monothioacetals with triethylsilane and silylated carbon nucleophiles, respectively, to afford the corresponding sulfide derivatives in good to high yields.
A CONVENIENT METHOD FOR THE PREPARATION OF γ-KETOSULFIDES FROM THIOACETALS
Ohshima, Masahiro,Murakami, Masahiro,Mukaiyama, Teruaki
, p. 1871 - 1874 (2007/10/02)
In the presence of trityl tetrafluoroborate, silyl enol ethers react with thioacetals to give the corresponding γ-ketosulfides in good yields with high stereoselectivity.In a similar manner, γ-ketosulfides are obtained in good yields by the one pot reacti
