Advertisement

Chemistry of Natural Compounds

, Volume 4, Issue 3, pp 132–135 | Cite as

Triterpene glycosides ofLeontice eversmannii

IV. Structure of leontoside D
  • L. G. Mzhel'skaya
  • N. K. Abubakirov
Article
  • 29 Downloads

Conclusions

The structure of leontoside D-a hederagenin pentaoside-has been established. The O-glycosidic moiety of leontoside D is O-β-D-glucopyranosido-(1 → 4)-O-α-L-arabopyranose, and the O-acyl moiety is O-α-L-rhamnopyranosido-(1 → 4)-O-β-D-glucopyranosido-(1 → 6)-O-β-D-glucopyranose.

Keywords

Glycoside TRITERPENE Glycoside Mixed Melting Point Lithium Aluminum Hydride Hederagenin 

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.
    L. G. Mzhel'skaya and N. K. Abubakirov, KhPS [Chemistry of Natural Compounds],3, 101, 1967.CrossRefGoogle Scholar
  3. 3.
    L. G. Mzhel'skaya and N. K. Abubakirov, KhPS [Chemistry of Natural Compounds],3, 218, 1967.CrossRefGoogle Scholar
  4. 4.
    V. G. Bukharov, V. V. Karlin, and V. A. Talan, KhPS [Chemistry of Natural Compounds],3, 17, 1967.Google Scholar
  5. 5.
    R. Kuhn, H. Trischmann, and I. Low, Angew. Chem.,67, 32, 1955.CrossRefGoogle Scholar
  6. 6.
    J. Polonsky, E. Sach, and E. Lederer, Bull. Soc. Chim. France,880, 1959.Google Scholar
  7. 7.
    A. Ya. Khorlin, A. G. Ven'yaminova, and N. K. Kochetkov, DAN SSSR,155, 619, 1964; Izv. AN SSSR, ser. khim.,1447, 1964;1588, 1966.Google Scholar
  8. 8.
    J. J. Scheidegger and E. Cherbuliez, Helv. Chim. Acta,38, 547, 1955.CrossRefGoogle Scholar
  9. 9.
    R. Tschesche, W. Schmidt, and G. Wulff, Z. Naturforsch.,208, 708, 1965.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