72653-51-1Relevant articles and documents
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
α-Alkylation and α-alkylidenation of carbonyl compounds: Lewis acid-promoted phenylthioalkylation of o-silylated enolates
Paterson, Ian,Fleming, Ian
, p. 2179 - 2182 (2007/10/11)
The O-silylated enolates of ketones, aldehydes, esters, and lactones can be phenylthioalkylated in the presence of Lewis acids; reductive or oxidative sulphur-removal gives the regiospecifically α-alkylated or alkylidenated carbonyl compounds.