Chemistry of Natural Compounds

, Volume 4, Issue 4, pp 186–189 | Cite as

Triterpene glycosides ofLeontice eversmannii

V. The structure of leontoside E
  • L. G. Mzhel'skaya
  • N. K. Abubakirov
Article

Conclusions

The structure of leontoside E has been established as a hexaoside of hederagenin. Its O-glycosidic moiety is branched and consists of O-β-D-glucopyranosido(1 » 4)-O-β-D-glucopyranosido(1 » 3)-O-α-L-arabopyranose and its O-acyl glycosidic moiety is O-α-L-rhamnopyranosido(1 » 4)-O-β-D-glucopyranosido(1 » 6)-O-β-D-glucopyranose.

Keywords

Glycoside Carboxy Group Carbohydrate Chain Silver Oxide Methyl Ethyl Ketone 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    L. G. Mzhel'skaya, V. K. Yatsyn, and N. K. Abubakirov, KhPS [Chemistry of Natural Compounds],2, 421, 1966.Google Scholar
  2. 2.
    V. G. Bukharov, V. V. Karlin, and V. A. Talan, KhPS [Chemistry of Natural Compounds],3, 17, 1967.Google Scholar
  3. 3.
    L. G. Mzhel'skaya and N. K. Abubakirov, KhPS [Chemistry of Natural Compounds],3, 101, 218, 1967;4, no. 3, 1968.Google Scholar
  4. 4.
    J. Polonsky, E. Sach, and E. Lederer, Bull. Soc. Chim. France, 880, 1959.Google Scholar
  5. 5.
    A. Ya. Khorlin, A. G. Ven'yaminova, and N. K. Kochetkov, Izv. AN SSSR, ser. khim., 1588, 1966.Google Scholar
  6. 6.
    R. Tschesche, W. Schmidt, and G. Wulff, Z. Naturf.,20b, 708, 1965.Google Scholar
  7. 7.
    N. K. Kochetkov and A. Ya. Khorlin, DAN SSSR,150, 1289, 1963, N. K. Kochetkov and A. J. Khorlin, Arzneim.-Forsch.,16, 101, 1966.Google Scholar
  8. 8.
    L. Hough, S. K. N. Jones, and W. H. Wadman, J. Chem. Soc., 1702, 1950.Google Scholar
  9. 9.
    T. G. Bonner, Chem. Ind., 345, 1960.Google Scholar

Copyright information

© The Faraday Press, Inc. 1971

Authors and Affiliations

  • L. G. Mzhel'skaya
    • 1
  • N. K. Abubakirov
    • 1
  1. 1.Institute of the Chemistry of Plant Substances AS UzSSRUSSR

Personalised recommendations