Chemistry of Natural Compounds

, Volume 22, Issue 6, pp 684–686 | Cite as

Alkaloids of the roots of theHaplophyllum obtusifolium

  • I. A. Bessonova
  • S. Yu. Yunusov
Article
  • 27 Downloads

Abstract

The roots of theHaplophyllum obtusifolium Ledeb. have yielded robustine, dictamnine, skimmianine, γ-fagarine, and evoxine and the new alkaloid haplobine for which on the basis of spectral characteristics and a passage to the main alkaloid haplopine (7-hydroxy-4,8-dimethoxyfuranoquinoline) the structure of 7-(3′-chloromethylbut-2′-enyloxy)-4,8-dimethoxyfuranoquinoline has been established.

Keywords

Alkaloid Cotton Seed Furan Ring Azocasein Acridone 

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Literature cited

  1. 1.
    I. A. Bessonova, D. Kurbanov, and S. Yu. Yunusov, Khim. Prir. Soedin., 124 (1984).Google Scholar
  2. 2.
    R. A. W. Johnstone, Mass Spectrometry for Organic Chemists, Cambridge University Press (1972); R. M. Silverstein, G. C. Bassler, and T. Morrill, Spectrometric Identification of Organic Compounds, 3rd edn., Wiley, New York (1974).Google Scholar
  3. 3.
    A. Ya. Revo, Qualitative Microchemical Reactions in Organic Chemistry [in Russian], Moscow (1965), p. 28.Google Scholar
  4. 4.
    I. A. Bessonova and S. Yu. Yunusov, Khim. Prir. Soedin., 303 (1977).Google Scholar
  5. 5.
    K. C. Engvild, Phytochemistry,25, 781 (1986).CrossRefGoogle Scholar
  6. 6.
    J. Reisch, Zs. Rozsa, K. Szendrei, I. Novak, and E. Minker, Phytochemistry,11, 2359 (1972);16, 151 (1977).CrossRefGoogle Scholar

Copyright information

© Plenum Publishing Corporation 1987

Authors and Affiliations

  • I. A. Bessonova
  • S. Yu. Yunusov

There are no affiliations available

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