Chemistry of Natural Compounds

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

Stereochemistry of latilobinol

  • A. Z. Abyshev
Article
First Online:
Received:
  • 31 Downloads

Abstract

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.

Keywords

Coumarin Nuclear Magnetic Resonance Spectrum Radius Vector Nuclear Magnetic Resonance Spectroscopy Cyclohexane Ring 
This is a preview of subscription content, log in to check access

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

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).CrossRefGoogle 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

There are no affiliations available

Personalised recommendations