Protonation of some cyclic β-Aminovinylthiones and β-aminovinylketones

  • L. I. Lavlinskaya
  • V. A. Pestunovich
  • Ya. S. Tsetlin
  • V. A. Usov
  • M. G. Voronkov
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Conclusions

The NMR method was used to study the protonation of 3-N,N-dimethylammo-5,5-dimethyl-3-cyclohexene-1-thione, 3-N,N-dimethylamino-2-phenylidene-1-thione, and their oxygen analogs. The protonation center for these compounds is different, and is, respectively, N and O, and S and 2-C.

Keywords

Oxygen Oxygen Analog 
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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Literature cited

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    L. I. Lavlinskaya, E. O. Tsetlina, V. A. Pestunovich, V. A. Usov, Ya. S. Tsetlin, and M. G. Voronkov, Izv. Akad. Nauk SSSR, Ser. Khim., 2108 (1975).Google Scholar

Copyright information

© Plenum Publishing Corporation 1977

Authors and Affiliations

  • L. I. Lavlinskaya
    • 1
  • V. A. Pestunovich
    • 1
  • Ya. S. Tsetlin
    • 1
  • V. A. Usov
    • 1
  • M. G. Voronkov
    • 1
  1. 1.Irkutsk Institute of Organic ChemistrySiberian Branch of the Academy of Sciences of the USSRUSSR

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