Advertisement

Chemistry of Heterocyclic Compounds

, Volume 15, Issue 5, pp 493–495 | Cite as

Oxidative imination of sulfur-containing heterocycles

  • S. S. Gontar'
  • G. I. Druzhinina
  • M. M. Kremlev
  • N. D. Borodavko
  • A. P. Kabakov
Article
  • 25 Downloads

Abstract

For the first time, the sulfur heteroatom of 4-oxothiazolidines has been iminated with sodium salts of chloroamides of arenesulfonic acids and N-chloroamides of carboxylic acids. The effect of the substituents and the size of the ring on the ability of the ring sulfur atom to undergo oxidative imination was studied.

Keywords

Sodium Sulfur Organic Chemistry Carboxylic Acid Sulfur Atom 
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.
    A. P. Dyban and L. P. Demkiv, Dokl. Akad. Nauk SSSR,99, 877 (1954).Google Scholar
  2. 2.
    F. C. Brown, Chem. Rev.,61, 463 (1961).Google Scholar
  3. 3.
    N. A. Shpakunova, E. A. Pidtoptannaya, N. P. Dolichuk, S. S. Kandabarova, M. M. Kremlev, and G. I. Druzhinina, Summaries of Papers Presented at the All-Union Scientific-Technical Conference on the Principal Pathways for Increasing the Quality of Rubbers on the Basis of the Application of Modern Elastomer Systems [in Russian], (1976), p. 50.Google Scholar
  4. 4.
    R. B. Grenwald, D. H. Evans, and J. R. De Member, Tetrahedron Lett.,45, 885 (1975).Google Scholar
  5. 5.
    A. G. Kostsova, Tr. Voronezhsk. Gos. Univ., No. 8, 92 (1935).Google Scholar
  6. 6.
    J. Shah, Can J. Chem.,53, 2381 (1975).Google Scholar
  7. 7.
    Y. Tamura, Y. Nishikawa, M. Ikeda Sumotok, M. Murase, and M. Kise, J. Org. Chem.,42, 3226 (1977).Google Scholar
  8. 8.
    E. S. Levchenko and I. N. Berzina, Zh. Org. Khim., No. 11, 2273 (1970).Google Scholar
  9. 9.
    E. T. Kaiser, M. Panar, and F. H. Westheimer, J. Am. Chem. Soc.,85, 602 (1963).Google Scholar
  10. 10.
    A. J. Fava, A. Illiceto, and E. Camera, J. Am. Chem. Soc.,79, 833 (1957).Google Scholar
  11. 11.
    J. A. Baltrop, J. Am. Chem. Soc.,76, 4348 (1954).Google Scholar
  12. 12.
    M. Calvin, Fed. Proc.,13, 697 (1954).Google Scholar
  13. 13.
    J. C. Sheehan, H. W. Hill, and E. L. Buhle, J. Am. Chem. Soc.,73, 4373 (1951).Google Scholar
  14. 14.
    J. Goerdeler and H. W. Linden, Tetrahedron Lett., No. 39, 3387 (1975).Google Scholar

Copyright information

© Plenum Publishing Corporation 1979

Authors and Affiliations

  • S. S. Gontar'
    • 1
  • G. I. Druzhinina
    • 1
  • M. M. Kremlev
    • 1
  • N. D. Borodavko
    • 1
  • A. P. Kabakov
    • 1
  1. 1.F. É. Dzerzhinskii Dnepropetrovsk Institute of Chemical TechnologyDnepropetrovsk

Personalised recommendations