Issue 7, 1971

C–C bond cleavage reactions of episulphones. A convenient new synthesis of thiepin 1,1-dioxide

Abstract

The reaction of vinyldiazomethane and its derivatives with sulphur dioxide and sulphenes yields dihydrothiepin 1,1-dioxide which are useful precursors to thiepin 1,1-dioxides; the probable intermediacy of divinyl episulphones in these reaction is discussed.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 313-314

C–C bond cleavage reactions of episulphones. A convenient new synthesis of thiepin 1,1-dioxide

L. A. Paquette and S. Maiorana, J. Chem. Soc. D, 1971, 313 DOI: 10.1039/C29710000313

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