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Three-electron transition to nitrophenylsulfenyl chlorides

  • N. T. Ioffe
  • M. I. Kalinkin
  • Z. V. Todres
Brief Communications

Conclusions

Electron transfer to o- and p-nitrophenylsulfenyl chloride results in a two-electron reduction of group S-Cl with a subsequent formation of anion radicals of nitrothiophenolates.

Keywords

Chloride Electron Transfer Anion Radical Subsequent Formation Nitrothiophenolates 
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.

Literature cited

  1. 1.
    D. N. Kursanov, Z. N. Parnes, N. T. Ioffe, M. I. Kalinkin, Z. V. Todres, and V. A. Tsyryapkin, Dokl. Akad. Nauk SSSR,187, 1064 (1969).Google Scholar
  2. 2.
    A. Maki and D. Geske, J. Am. Chem. Soc.,83, 1852 (1961).Google Scholar
  3. 3.
    K. Umemoto, Y. Deguchi, and T. Fujinaga, Bull. Chem. Soc. Japan,36, 1539 (1963).Google Scholar

Copyright information

© Consultants Bureau 1971

Authors and Affiliations

  • N. T. Ioffe
    • 1
  • M. I. Kalinkin
    • 1
  • Z. V. Todres
    • 1
  1. 1.Institute of Heteroorganic CompoundsAcademy of Sciences of the USSRUSSR

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