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Chemistry of Heterocyclic Compounds

, Volume 4, Issue 4, pp 470–471 | Cite as

Formation of an acyclic disulfide from an 4-acylamino-3-oxothiophan

  • S. D. Mikhno
  • V. M. Berezovskii
Article
  • 30 Downloads

Abstract

It has been established that 4-benzoylamino-3-oxothiophan is cleaved at a S-C bond by methanol in the presence of sodium methoxide with the formation of an acyclic disulfide.

Keywords

Sodium Methanol Organic Chemistry Disulfide Methoxide 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

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    W. Kerp, Ber., 28, 1476, 1895.Google Scholar
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    P. Karer and H. Schmid, Helv. Chim. Acta, 27, 1275, 1944.Google Scholar
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    I. Cimerman and I. Willis, J. Chem. Soc., 1332, 1951.Google Scholar

Copyright information

© Consultants Bureau 1971

Authors and Affiliations

  • S. D. Mikhno
    • 1
  • V. M. Berezovskii
    • 1
  1. 1.All-Union Scientific-Research Vitamin InstituteMoscow

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