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Chemistry of Natural Compounds

, Volume 11, Issue 6, pp 715–719 | Cite as

Hydroxystilbenes of the inner bark of Pinus sibirica

  • A. S. Gromova
  • N. A. Tyukavkina
  • V. I. Lutskii
  • G. A. Kalabin
  • D. F. Kushnarev
Article

Summary

In addition to pinostilbene and resveratrol, two new stilbene glycosides have been isolated from the phloem ofPinus sibirica R. Mayr, and their structures have been established as 3,4′-dihydroxy-5-methoxy-stilbene 4′-β-D-glycopyranoside (pinostilbenoside) and 3,4′,5-trihydroxystilbene 4′-β-D-glycopyranoside (resveratroloside).

Keywords

Resveratrol Stilbene Methyl Ether Anomeric Proton Monomethyl Ether 

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Literature cited

  1. 1.
    N. A. Tyukavkina, A. C. Gromova, V. I. Lutskii, and V. K. Voronov, Khim. Prirodn. Soedin., 600 (1972).Google Scholar
  2. 2.
    H. Gusten and M. Salzwedel, Tetrahedron,23, 173 (1967).CrossRefGoogle Scholar
  3. 3.
    H. J. Ranfs and D. W. Cameron, Austr. J. Chem.,24, 2427 (1971).CrossRefGoogle Scholar
  4. 4.
    H. Spiesecke and W. G. Schneider, J. Chem. Phys.,35, 731 (1961).CrossRefGoogle Scholar
  5. 5.
    M. Zanger, Org. Res.,4, 1 (1972).CrossRefGoogle Scholar
  6. 6.
    W. Brugel, NMR Spectra and Chemical Structure, Academic Press, New York, Vol. 1 (1967), p. 15.Google Scholar
  7. 7.
    J. D. Stevens and H. G. Fletcher, J. Org. Chem.,33, 1795 (1968).Google Scholar
  8. 8.
    B. Casu, M. Reggiani, G. G. Gallo, and A. Vigevani, Tetrahedron,22, 3061 (1966).CrossRefGoogle Scholar
  9. 9.
    T. D. Inch, Annual Reports on NMR Spectrometry,5A, 305 (1972).CrossRefGoogle Scholar
  10. 10.
    A. S. Gromova, V. I. Lytskii, and N. A. Tyukavkina, Khim. Prirodn. Soedn., 778 (1974).Google Scholar
  11. 11.
    W. Klyne, Biochem. J.,47, No. 4, xli (1950).Google Scholar
  12. 12.
    E. Rudloff and P. Jorgensen, Phytochem.,2, 297 (1963).CrossRefGoogle Scholar

Copyright information

© Plenum Publishing Corporation 1976

Authors and Affiliations

  • A. S. Gromova
  • N. A. Tyukavkina
  • V. I. Lutskii
  • G. A. Kalabin
  • D. F. Kushnarev

There are no affiliations available

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