87910-10-9Relevant academic research and scientific papers
A Novel Method of Crossed-Aldol Condensation: Alkylation of Trimethylsilyl Enol Ethers by Alkyl 1-Chloro-2-arylthioalkyl Ethers
Ibragimov, M. A.,Lazareva, M. I.,Smit, W. A.
, p. 880 - 884 (2007/10/02)
Trimethylsilyl enol ethers 5, derived from aldehydes or ketones, react with alkyl 1-chloro-2-arylthioalkyl ethers 3 (β-arylthio-α-chloroethers, prepared in situ from vinyl ethers 1 and arenesulfenyl chlorides 2) to give 2-alkoxy-3-arylthioalkyl ketone derivatives 6 in the presence of a Lewis acid.
REACTION OF SILYL ENOL ETHERS WITH β-HALOGENOALKYL ARYL SULFIDES - A METHOD OF β-ARYLTHIOALKYLATION OF CARBONYL COMPOUNDS
Ibragimov, M.A.,Smit, W.A.
, p. 961 - 964 (2007/10/02)
Reaction of β-halogenoalkyl aryl sulfides with silyl enol ethers in the presence of Lewis acids produced α-(β'-arylthioalkyl) substituted carbonyl compounds.
