Issue 6, 1990

A novel route to 1,2-benzothiazin-4-ones involving s-dealkylation of an arylalkyl sulphide

Abstract

A novel preparation of the sulphenylimine, 1,2-benzothiazine-4-one involving sequential nucleophilic displacement of a toluene-p-sulphonate group from an oxime tosylate and dealkylation of an arylalkyl sulphide is reported; a possible mechanism is presented.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 497-498

A novel route to 1,2-benzothiazin-4-ones involving s-dealkylation of an arylalkyl sulphide

S. Jones, P. D. Kennewell, R. Westwood and P. G. Sammes, J. Chem. Soc., Chem. Commun., 1990, 497 DOI: 10.1039/C39900000497

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