Chemistry of Natural Compounds

, Volume 20, Issue 6, pp 674–677 | Cite as

Stereochemistry of latilobinol

  • A. Z. Abyshev


The results are given of a study of the stereochemistry of a coumarin terpenoid derivative — latilobinol — by nuclear magnetic resonance spectroscopy using lanthanoid shift reagents. On the basis of the results obtained, it has been established that the hydroxy group in the cyclohexane ring occupies the equatorial position.


Coumarin Nuclear Magnetic Resonance Spectrum Radius Vector Nuclear Magnetic Resonance Spectroscopy Cyclohexane Ring 


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Literature cited

  1. 1.
    A. Z. Abyshev, Khim. Prir. Spedin., 90 (1979).Google Scholar
  2. 2.
    C. C. Hinckley, J. Am. Chem. Soc.,91, 5160 (1969).CrossRefPubMedPubMedCentralGoogle Scholar
  3. 3.
    J. M. Armitage and D. Hall, J. Am. Chem. Soc.,95, 1437 (1973).CrossRefGoogle Scholar
  4. 4.
    C. C. Hinckley, M. R. Klotz, and F. Patil, J. Am. Chem. Soc.,93, 2417 (1971).CrossRefGoogle Scholar
  5. 5.
    J. K. M. Saunders and D. H. Williams, J. Am. Chem. Soc.,93, 641 (1971).CrossRefGoogle Scholar
  6. 6.
    L. Fieser and M. Fieser, Steroids, Reinhold, New York (1959).Google Scholar
  7. 7.
    A. I. Saidkhodzhaev, Khim. Prir. Soedin., 4 (1979).Google Scholar

Copyright information

© Plenum Publishing Corporation 1985

Authors and Affiliations

  • A. Z. Abyshev

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