Issue 15, 1980

Nitrile sulphide formation from the thermal fragmentation of 1,3,4-oxathiazoles: a retro-1,3-dipolar cycloaddition

Abstract

1,3,4-Oxathiazoles, on thermolysis, undergo retro-1,3-dipolar cycloaddition to afford carbonyl compounds and nitrile sulphides, which may be trapped by cycloaddition with alkynes and nitriles.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 714-715

Nitrile sulphide formation from the thermal fragmentation of 1,3,4-oxathiazoles: a retro-1,3-dipolar cycloaddition

R. M. Paton, F. M. Robertson, J. F. Ross and J. Crosby, J. Chem. Soc., Chem. Commun., 1980, 714 DOI: 10.1039/C39800000714

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