Chemistry of Natural Compounds

, Volume 15, Issue 5, pp 587–591 | Cite as

Triterpene glycosides ofScabiosa soongorica

IV. Partial synthesis of songoroside A and of bisglycosides of oleanolic acid
  • A. A. Akimaliev
  • N. Sh. Pal'yants
  • P. K. Alimbaeva
  • N. K. Abubakirov
Article
  • 24 Downloads

Abstract

Partial syntheses of glycosides of oleanolic acid — the 3-0-β-D-xylopyranoside (songoroside A), the 3,28-bis-0-β-D-xylopyranoside, and the 28-0-β-gentiobioside-3-0-β-D-xylopyranoside — and also the formation of 3-0-β-D-xylopyranosyloleanolic acid 13,28-lactone are described.

Keywords

Oleanolic Acid Sodium Methanolate Mercuric Oxide Silver Carbonate Anhydrous Calcium Sulfate 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    A. Akimaliev, P. K. Alimbaeva, L. G. Mzhel'skaya, and N. K. Abubakirov, Khim. Prir. Soedin., 472, 476 (1976).Google Scholar
  2. 2.
    V. G. Bukharov and V. V. Karlin, Khim. Prir. Soedin., 84 (1969).Google Scholar
  3. 3.
    S. J. Stolzenberg, R. M. Parkhurst, and E. J. Reist, Contraception,14, 39 (1976).CrossRefGoogle Scholar
  4. 4.
    A. M. Yuodvirshis and A. T. Troshchenko, Izv. Sib. Otd. Akad. Nauk SSSR, Ser. Khim. Nauk, No. 2, 129 (1969).Google Scholar
  5. 5.
    K. Takamura, Chem. Pharm. Bull.,4, 470 (1956).CrossRefGoogle Scholar
  6. 6.
    A. F. Bochkov and L. G. Kretsu, Izv. Akad. Nauk SSSR, Ser. Khim., 2803 (1971).Google Scholar
  7. 7.
    E. Hardegger and F. Robinet, Helv. Chem. Acta,33, 1871 (1950);35, 824 (1952).CrossRefGoogle Scholar
  8. 8.
    A. Ya. Khorlin, Yu. S. Ovodov, and N. K. Kochetkov, Zh. Obshch. Khim.,32, 782 (1962).Google Scholar
  9. 9.
    R. U. Lemieux and J. D. Stevens, Can. J. Chem.,44, 249 (1966).CrossRefGoogle Scholar
  10. 10.
    H. P. Albrecht, Ann. Chem., 1429 (1977).Google Scholar
  11. 11.
    A. F. Sviridov, L. P. Vecherko, V. I. Kadentsev, O. S. Chizhov, and N. K. Kochetkov, Izv. Akad. Nauk SSSR, Ser. Khim., 2713 (1973).Google Scholar
  12. 12.
    V. T. Chernobai, Zh. Obshch. Khim.,34, 1018 (1964).Google Scholar
  13. 13.
    B. Helferich and M. Gindy, Chem. Ber.,87, 1489 (1954).Google Scholar
  14. 14.
    K. Takiura, S. Honda, T. Endo, and K. Kakehi, Chem. Pharm. Bull.,20, 438 (1972).CrossRefGoogle Scholar
  15. 15.
    J. Becker, Biochim. Biophys. Acta,100, 574 (1965).CrossRefGoogle Scholar
  16. 16.
    Yu. V. Karyakin, Pure Chemical Reagents [in Russian], Moscow-Leningrad (1947), p. 454.Google Scholar

Copyright information

© Plenum Publishing Corporation 1980

Authors and Affiliations

  • A. A. Akimaliev
  • N. Sh. Pal'yants
  • P. K. Alimbaeva
  • N. K. Abubakirov

There are no affiliations available

Personalised recommendations