Issue 9, 1989

Carbon–carbon bond forming desulphurisation of a tetrathiane

Abstract

The 1,2,4,5-tetrathiane (3), readily formed from amido ester (2) and disulphur dichloride, undergoes immediate reaction with potassium hydroxide in ethanol at room temperature to form sulphur and the maleimide salt (6) which is characterised as its S-benzyl and S-methyl (4) derivatives; a mechanism is proposed for this mild carbon–carbon bond forming desulphurisation reaction.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 1699-1700

Carbon–carbon bond forming desulphurisation of a tetrathiane

R. M. Bannister and C. W. Rees, J. Chem. Soc., Perkin Trans. 1, 1989, 1699 DOI: 10.1039/P19890001699

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