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).
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N. A. Tyukavkina, A. C. Gromova, V. I. Lutskii, and V. K. Voronov, Khim. Prirodn. Soedin., 600 (1972).
H. Gusten and M. Salzwedel, Tetrahedron,23, 173 (1967).
H. J. Ranfs and D. W. Cameron, Austr. J. Chem.,24, 2427 (1971).
H. Spiesecke and W. G. Schneider, J. Chem. Phys.,35, 731 (1961).
M. Zanger, Org. Res.,4, 1 (1972).
W. Brugel, NMR Spectra and Chemical Structure, Academic Press, New York, Vol. 1 (1967), p. 15.
J. D. Stevens and H. G. Fletcher, J. Org. Chem.,33, 1795 (1968).
B. Casu, M. Reggiani, G. G. Gallo, and A. Vigevani, Tetrahedron,22, 3061 (1966).
T. D. Inch, Annual Reports on NMR Spectrometry,5A, 305 (1972).
A. S. Gromova, V. I. Lytskii, and N. A. Tyukavkina, Khim. Prirodn. Soedn., 778 (1974).
W. Klyne, Biochem. J.,47, No. 4, xli (1950).
E. Rudloff and P. Jorgensen, Phytochem.,2, 297 (1963).
Additional information
Irkutsk Institute of Organic Chemistry, Siberian Branch of the Academy of Sciences of the USSR. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 677–682, November–December, 1975.
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Gromova, A.S., Tyukavkina, N.A., Lutskii, V.I. et al. Hydroxystilbenes of the inner bark of Pinus sibirica. Chem Nat Compd 11, 715–719 (1975). https://doi.org/10.1007/BF00568450
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DOI: https://doi.org/10.1007/BF00568450