Advertisement

Chemistry of Natural Compounds

, Volume 9, Issue 4, pp 472–474 | Cite as

Structure of veralosidinine

  • R. Shakirov
  • S. Yu. Yunusov
Article

Summary

On the basis of the IR, UV, NMR, and mass spectra of veralosidinine and its conversion products its most probable structure and configuration have been established as 16α-acetyl-22,26-nitrilocholesta-5,22(N)-diene-3β, 15β-diol.

Keywords

Acetic Anhydride Olefinic Proton Epigeal Part PtO2 Amino Alcohol 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    R. Shakirov and S. Yu. Yunusov, Khim. Prirodn. Soedin., 852 (1971).Google Scholar
  2. 2.
    A. M. Khashimov, R. Shakirov, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 779 (1971).Google Scholar
  3. 3.
    Q. Adam, K. Schreiber, J. Tomko, and A. Vassova, Tetrahedron,23, 167 (1967).CrossRefGoogle Scholar
  4. 4.
    A. M. Khashimov, R. Shakirov, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 339 (1970).Google Scholar
  5. 5.
    E. Bianchi, C. Djerassi, H. Budzikiewicz, and Y. Sato, J. Org. Chem.,30, 754 (1965).CrossRefGoogle Scholar
  6. 6.
    R. N. Nuriddinov, B. Babaev, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 604 (1969).Google Scholar
  7. 7.
    Y. Sato, Y. Sato, H. Kaneko, E. Bianchi, and H. Kataoka, J. Org. Chem.,34, 1577 (1969).CrossRefGoogle Scholar
  8. 8.
    T. Masamune, Y. Mori, M. Takasugi, A. Mural, S. Ohuchit, N. Sato, and N. Katsui, Bull. Chem. Soc., Japan,38, 1374 (1965).CrossRefGoogle Scholar
  9. 9.
    J. Tomko, Z. Voticky, H. Budzikiewicz, and F. J. Darkan, Coll.,10, 3320 (1965).Google Scholar
  10. 10.
    R. F. Zürcher, Helv. Chim. Acta,46, 2054 (1963).CrossRefGoogle Scholar
  11. 11.
    W. M. Stokes and W. Bergmann, J. Org. Chem.,17, 1194 (1952).CrossRefGoogle Scholar

Copyright information

© Plenum Publishing Corporation 1975

Authors and Affiliations

  • R. Shakirov
  • S. Yu. Yunusov

There are no affiliations available

Personalised recommendations