Chemistry of Natural Compounds

, Volume 15, Issue 3, pp 269–272 | Cite as

New acylated flavone glycoside fromGnaphalium uliginosum

  • M. M. Konopleva
  • L. P. Smirnova
  • V. T. Glyzin
  • V. L. Shelyuto


A new acylated flavone glycoside has been isolated for the first time from the herb marsh cudweed, and for it the structure of 6″-caffeyl-7-β-D-glucopyranosyloxy-4′,5-dihydroxy-3′,6′dimethoxyflavone has been established. In addition, the aglycone, identified as 4′,5,7-trihydroxy-3′,6-dimethoxyflavone has been isolated. The identifications were made on the basis of UV, IR, PMR, and mass spectra, the products of alkaline and acid hydrolyses, and the results of elementary analysis, melting points, and specific rotations.


Mass Spectrum Organic Chemistry Melting Point Glycoside Acid Hydrolysis 
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Literature cited

  1. 1.
    A. D. Turova, Medicinal Plants of the USSR and Their Use [in Russian], Moscow (1974), pp. 256–259.Google Scholar
  2. 2.
    H. Audier, “Étude des composés flavoniques par spectrometrie de masse,” Bull. Soc. Chim. Fr., No. 9, 2892 (1966).Google Scholar
  3. 3.
    S. Nataraian, V. V. S. Murti, and T. R. Seshadri, “Biflavonyls; Part III — mass spectrometry of biflavones,” Indian J. Chem.,7, 751 (1969).Google Scholar
  4. 4.
    J. W. Apsimon, V. B. Haynes, K. V. Sim, and W. B. Whalley, J. Chem. Soc., 3780 (1963).Google Scholar

Copyright information

© Plenum Publishing Corporation 1979

Authors and Affiliations

  • M. M. Konopleva
  • L. P. Smirnova
  • V. T. Glyzin
  • V. L. Shelyuto

There are no affiliations available

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