Chemistry of Natural Compounds

, Volume 8, Issue 3, pp 278–281 | Cite as

Flavonoids of asperula oppositifolia

  • M. I. Borisov
  • A. G. Serbin
  • N. F. Komissarenko
Article

Summary

A flavonoid glycoside which has been called oppositifolin has been isolated from the herbAsperula oppositifolia Rgl. et Schmalh. It has been assigned the most probable structure of chrysoeriol 7-O-β-D-mannopyranosyl-(1 → 2)-β-D-(6-acetylglucopyranoside). Desacetyloppositifolin [chrysoeriol 7-O-β-D-mannopyranosyl-(1 → 2)-β-D-glucopyranoside] and the corresponding monoside (chrysoeriol 7-O-β-D-glucopyranoside) have been obtained and isolated by chromatography on Kapron.

Keywords

Glycoside Luteolin Vanillic Acid Phloroglucinol Sulfanilic Acid 

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Literature cited

  1. 1.
    L. Bellamy, Infra-Red Spectra of Complex Molecules, 2nd ed., Methuen (1958).Google Scholar
  2. 2.
    L. I. Borodin, V. I. Litvinenko, and N. V. Kurinna, Farm. Zh.,1970, No. 2, 62.Google Scholar
  3. 3.
    M. I. Borisov and Yu. G. Borisyuk, Farm. Zh.,1963, No. 4, 75.Google Scholar
  4. 4.
    Houben-Weyl, Methoden der Organischen Chemie (Analytische Methoden), Georg Thieme Verlag, Stuttgart.Google Scholar
  5. 5.
    W. Karrer, Konstitution und Vorkommen der Organischen Pflanzenstoffe, Birkhäuser Verlag, Basel und Stuttgart (1958), p. 596.CrossRefGoogle Scholar
  6. 6.
    V. I. Litvinenko and N. P. Maksyutina, Khim. Prirodn. Soedin., 420 (1965).Google Scholar
  7. 7.
    L. I. Deryugin, N. P. Maksyutina, and P. E. Krivenchuk, Khim. Prirodn. Soedin., 394 (1966).Google Scholar
  8. 8.
    L. G. Mzhel'skaya and N. K. Abubakirov, Khim. Prirodn. Soedin., 101 (1967).Google Scholar
  9. 9.
    N. P. Maksyutina and V. I. Litvinenko, Khim. Prirodn. Soedin., 20 (1966).Google Scholar
  10. 10.
    M. P. Khare, O. Schindler, and T. Reichstein, Helv. Chim. Acta, 1544 (1962).Google Scholar
  11. 11.
    V. I. Litvinenko and V. A. Makarov, Khim. Prirodn. Soedin., 366 (1969).Google Scholar
  12. 12.
    T. A. Sergienko, L. S. Kazarnovskii, and V. I. Litvinenko, Farmatsiya,1967, 34.Google Scholar
  13. 13.
    I. P. Kovalev and V. I. Litvinenko, Khim. Prirodn. Soedin., 233 (1965).Google Scholar
  14. 14.
    V. N. Spiridonov, I. P. Kovalev, and A. P. Prokopenko, Khim. Prirodn. Soedin., 5 (1969).Google Scholar
  15. 15.
    I. I. Vinokurov and A. I. Skrigan, Izv. Akad. Nauk BSSR, Ser. Khim. N.,1969, No. 5, 112.Google Scholar
  16. 16.
    M. I. Borisov and N. F. Komissarenko, Khim. Prirodn. Soedin., 371 (1969).Google Scholar
  17. 17.
    S. M. Partridge, Nature,164, 443 (1949).CrossRefGoogle Scholar
  18. 18.
    P. Kuhn and H. Roth, Ber.,66, 1274 (1933).Google Scholar

Copyright information

© Consultants Bureau 1974

Authors and Affiliations

  • M. I. Borisov
  • A. G. Serbin
  • N. F. Komissarenko

There are no affiliations available

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