Advertisement

Chemistry of Natural Compounds

, Volume 34, Issue 5, pp 616–619 | Cite as

Low-molecular-mass metabolites of fungi. III. Stachybotrolide fromStachybotrys alternans

  • L. S. Kamalov
  • S. F. Aripova
  • M. I. Isaev
Article

Abstract

The new nitrogen-free compound stachybotrolide has been detected among the products of the vital activity ofStachybotrys alternans. The structure of stachybotrolide has been determined on the basis of IR, mass, and1H and13C NMR spectra. To interpret the latter we have made use of DEPT, 2M NMR1H−1H chemical shift correlation (1H−1H COSY or HMQC) and 2M NMR correlations of1H−13C long-range interactions (HMBC).

Keywords

Diacetate Acetic Anhydride Aromatic Proton HMBC Spectrum HMQC Spectrum 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    L. S. Kamalov, S. F. Aripova, and M. I. Isaev, Khim. Prir. Soedin., 599 (1997).Google Scholar
  2. 2.
    L. S. Kamalov, S. F. Aripova, and M. I. Isaev, Khim. Prir. Soedin., Spets. Vypusk [Special Issue], 4 (1997).Google Scholar
  3. 3.
    L. S. Kamalov, S. F. Aripova, and M. I. Isaev, Khim. Prir. Soedin., Spets. Vypusk [Special Issue], 7 (1998).Google Scholar
  4. 4.
    L. S. Kamalov, S. F. Aripova, B. Tashkhodzhaev, and M. I. Isaev, Khim. Prir. Soedin., 666 (1998) [this issue].Google Scholar
  5. 5.
    K. Nakanishi, Infrared Absorption Spectroscopy. Practical, Holden-Day, San Francisco (1962) [Russian tranlation, Mir, Moscow (1965), p. 56].Google Scholar

Copyright information

© Kluwer Academic/Plenum Publishers 1998

Authors and Affiliations

  • L. S. Kamalov
  • S. F. Aripova
  • M. I. Isaev

There are no affiliations available

Personalised recommendations