Formation of allyl sulphide synthons by [1,2] and [1,3] shifts of the phenylthio group

Abstract
Allyl phenyl sulphides, made from 2-hydroxy-alkyl phenyl sulphides by acid-catalysed rearrangement of the phenylthio group, may be isomerised by the [1,3] allylic shift of the same group, and converted into 4-hydroxy carbonyl compounds or allyl alcohols.

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