Chemistry of Natural Compounds

, Volume 12, Issue 6, pp 709–713 | Cite as

The structure of perfamine

  • D. M. Razakova
  • I. A. Bessonova
  • S. Yu. Yunusov
Article

Summary

1. The leaves and epigeal part ofHaplophyllum perforatum have yielded a new alkaloid perfamine — the first representative of the quinoline series in which the benzene ring is modified into a gem-disubstituted cyclohexadienone ring.

2. On the basis of spectral data, chemical transformations, and conversion into skimmianine, structure (I) has been established for perfamine.

Keywords

Methoxy Group Furan Ring Epigeal Part Caustic Soda Neutral Fraction 

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Literature cited

  1. 1.
    V. I. Akhmedzhanova, I. A. Bessonova, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 109 (1974).Google Scholar
  2. 2.
    D. M. Razakova, I. A. Bessonova, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 812 (1975).Google Scholar
  3. 3.
    Z. Sh. Faizutdinova, I. A. Bessonova, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 360 (1968).Google Scholar
  4. 4.
    V. V. Ershov, A. A. Volod'kin, and G. N. Bogdanov, Usp. Khim., No. 2, 154 (1963).Google Scholar
  5. 5.
    A. W. Sangster and K. L. Stuart, Chem. Rev.,65, 101 (1965).CrossRefGoogle Scholar
  6. 6.
    A. V. Robertson, Aust. J. Chem.,16, 451 (1963).CrossRefGoogle Scholar
  7. 7.
    Z. Sh. Faizutdinova and S. Yu. Yunusov, Khim. Prirodn. Soedin., 260 (1967).Google Scholar
  8. 8.
    D. M. Clugston and D. B. MacLean, Can. J. Chem.,43, 2516 (1965).CrossRefGoogle Scholar
  9. 9.
    Ya. V. Rashkes, Z. Sh. Faizutdinova, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 107 (1970).Google Scholar
  10. 10.
    I. A. Bessonova and S. Yu. Yunusov, Khim. Prirodn. Soedin., 52 (1974).Google Scholar

Copyright information

© Plenum Publishing Corporation 1977

Authors and Affiliations

  • D. M. Razakova
  • I. A. Bessonova
  • S. Yu. Yunusov

There are no affiliations available

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