Advertisement

α-Organylthiocrotonaldehydes

  • N. A. Keiko
  • L. G. Stepanova
  • I. D. Kalikhman
  • M. G. Voronkov
Brief Communications

Conclusions

A method was developed for the preparation of α-organylthiocrotonaldehydes based on the reaction of α-chlorocrotonaldehyde with aliphatic or aromatic thiols.

Keywords

Thiol Aromatic Thiol 
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.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    H. J. Monteiro and A. L. Gemal, Synth. Commun., 437 (1975).Google Scholar
  2. 2.
    J. H. S. Wheland and J. F. Arens, Recl. Trav. Chim.,75, 1358 (1956); Z. Kosarych and T. Cohen, Tetrahedron Lett.,21, 3959 (1980); L. Duhamel, J. Chauvin, and A. Messier, Tetrahedron Lett.,21, 4171 (1980).Google Scholar
  3. 3.
    N. A. Keiko, T. N. Mamashvili, G. V. Rassolova, T. V. Kashik, I. D. Kalikhman, and M. G. Voronkov, Izv. Akad. Nauk SSSR, Ser. Khim., 608 (1984); M. F. Shostakovskii, N. A. Keiko, and A. Kh. Filippova, Izv. Akad. Nauk SSSR, Ser. Khim., 392 (1967).Google Scholar
  4. 4.
    M. G. Voronkov, N. A. Keiko, L. G. Stepanova, G. I. Kirillova, T. N. Musorina, and I. D. Kalikhman, Izv. Akad. Nauk SSSR, Ser. Khim., 1204 (1975).Google Scholar
  5. 5.
    N. A. Keiko, L. G. Stepanova, N. I. Wainberg, O. B. Bannikova, and M. G. Voronkov, Zh. Irg. Khim.,19, 480 (1983).Google Scholar

Copyright information

© Plenum Publishing Corporation 1987

Authors and Affiliations

  • N. A. Keiko
    • 1
  • L. G. Stepanova
    • 1
  • I. D. Kalikhman
    • 1
  • M. G. Voronkov
    • 1
  1. 1.Irkutsk Institute of Organic ChemistrySiberian Branch of the Academy of Sciences of the USSRUSSR

Personalised recommendations