Chemistry of Natural Compounds

, Volume 8, Issue 1, pp 43–47 | Cite as

Gosferol — A new furocoumarin from the roots of Prangos ferulacea

  • A. Z. Abyshev
  • P. P. Denisenko
  • N. P. Kostyuchenko
  • A. I. Ermakov
  • Yu. N. Sheinker
Article
  • 48 Downloads

Summary

From the roots ofPrangos ferulacea (L.) Lindl. has been isolated a new furocoumarin (I), C10H14O5, with mp 136.5–138.5°C (from ethanol), [α] D 20 ± 0° (chloroform), which we have calledgosferol.

On the basis of a study of the UV, IR, NMR, and mass spectra and the chemical properties of gosferol, the structure 5-(2″-hydroxy-3″-methylbutenyloxy)furo-2′,3′:7,6-coumarin has been proposed for it.

Keywords

Acetic Anhydride Coumarin Derivative Activity Grade Mixed Melting Point Pyrone Ring 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    A. Z. Abyshev, Khim. Prirodn. Soedin.,5, 3 (1969).Google Scholar
  2. 2.
    W. L. Stanley, A. S. Waiss, J. R. E. Lundin, and S. H. Vannier, Tetrahedron,21, No. 1, 89 (1965).CrossRefGoogle Scholar
  3. 3.
    G. A. Kuznetsova, A. Z. Abyshev, M. E. Perel'son, Yu. N. Sheinker, and G. Yu. Pek, Khim. Prirodn. Soedin.,2, 310 (1966).Google Scholar
  4. 4.
    A. Z. Abyshev, P. P. Denisenko, N. P. Kostyuchenko, O. S. Anisimova, A. I. Ermakov, and Yu. N. Sheinker, Khim. Prirodn. Soedin.,6, 675 (1970).Google Scholar

Copyright information

© Consultants Bureau, a division of Plenum Publishing Corporation 1974

Authors and Affiliations

  • A. Z. Abyshev
  • P. P. Denisenko
  • N. P. Kostyuchenko
  • A. I. Ermakov
  • Yu. N. Sheinker

There are no affiliations available

Personalised recommendations