Carbon–carbon bond forming desulphurisation of a tetrathiane

doi:10.1039/P19890001699

Paper

Carbon–carbon bond forming desulphurisation of a tetrathiane

Published 1989 · R. Bannister, C. Rees

Journal of The Chemical Society-perkin Transactions 1

UNKNOWN SJR score

2

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0

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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.

Study Snapshot

This study proposes a mild carbon-carbon bond forming desulphurisation reaction for 1,2,4,5-tetrathiane (3), which undergoes immediate reaction with potassium hydroxide in ethanol at room temperature to form sulphur and maleimide salt (6).

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Carbon–carbon bond forming desulphurisation of a tetrathiane

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