130655-07-1Relevant articles and documents
Preparation and rearrangement of 2-allyloxyethyl aryl sulfoxides; a mercury-free claisen sequence
Mandai, Tadakatsu,Ueda, Masaki,Hasegawa, Shun-Ichi,Kawada, Mikio,Tsuji, Jiro,Saito, Seiki
, p. 4041 - 4044 (2007/10/02)
Alkali metal hydride promoted addition of allylic alcohols to aryl vinyl sulfoxides at room temperature gives 2-allyloxyethyl aryl sulfoxides, which, on heating, are converted into γ,δ-unsaturated aldehydes via allylic vinyl ethers.