Issue 19, 1976

Formation of allyl sulphides by phenylthio migration: effects of alkyl substitution and control by silicon

Abstract

The acid-catalysed rearrangement of β-hydroxyalkyl phenyl sulphides leads to phenylthio migration from a tertiary or secondary centre to a primary centre, and, when assisted by silicon, between two secondary centres or even from a secondary to a tertiary centre.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 751-752

Formation of allyl sulphides by phenylthio migration: effects of alkyl substitution and control by silicon

P. Brownbridge, I. Fleming, A. Pearce and S. Warren, J. Chem. Soc., Chem. Commun., 1976, 751 DOI: 10.1039/C39760000751

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