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Reaction for nucleophilic opening of thiirane ring by thiols

  • A. V. Fokin
  • A. F. Kolomiets
  • L. S. Rudnitskaya
  • V. I. Shevchenko
Brief Communications

Conclusions

The nucleophilic opening of the thiirane ring by thiols proceeds with greater difficulty than that of the oxirane ring. Aliphatic and aromatic thiols in nonpolar solvents, using homogeneous catalysis by bases, can be unambiguously mercaptoethylated by selecting the necessary ratios of thiol compound and ethylene sulfide.

Keywords

Ethylene Sulfide Catalysis Thiol Great Difficulty 
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.

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Copyright information

© Plenum Publishing Corporation 1975

Authors and Affiliations

  • A. V. Fokin
  • A. F. Kolomiets
  • L. S. Rudnitskaya
  • V. I. Shevchenko

There are no affiliations available

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