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Reaction of benzimidazole-2-thione with cyanoacetylene alcohols

  • G. G. Skvortsova
  • L. V. Andriyankova
  • N. D. Abramova
  • Yu. M. Skvortsov
  • A. G. Mal'kina
Brief Communications

Conclusions

2-Iminobenzimidazo-1,3-thiazines containing a hydroxyl group were obtained by the reaction of benzimid-azole-2-thione with tertiary cyanoacetylene alcohols. It was observed that they have enhanced stability toward alkalis.

Keywords

Alcohol Hydroxyl Thiazine Cyanoacetylene Cyanoacetylene Alcohol 
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

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    G. G. Skvortsova, N. D. Abramova, A. G. Mal'kina, Yu. M. Skvortsov, B. V. Trzhtsinskaya, and A. M. Albanov, Khim. Geterotsikl. Soedin., 963 (1982).Google Scholar
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Copyright information

© Plenum Publishing Corporation 1985

Authors and Affiliations

  • G. G. Skvortsova
    • 1
  • L. V. Andriyankova
    • 1
  • N. D. Abramova
    • 1
  • Yu. M. Skvortsov
    • 1
  • A. G. Mal'kina
    • 1
  1. 1.Irkutsk Institute of Organic Chemistry, Siberian BranchAcademy of Sciences of the USSRUSSR

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