Advertisement

Chemistry of Natural Compounds

, Volume 5, Issue 5, pp 305–306 | Cite as

The alkaline hydrolysis of flavonoid glycosides

  • V. I. Litvinenko
  • V. A. Makarov
Article
First Online:

Conclusions

1. The alkaline hydrolysis of flavonoid glycosides has been studied.

2. In an alkaline medium 3-glycosides, C-glycosides, and biosides having 1, 2 bonds between the sugars are stable.

3. The difference in the stabilities of the glycosides to alkalis can be used in studying flavonoid O-diglycosides, O-biosides with different positions of the bond, O,C-diglycosides, and O,C-biosides.

Keywords

Glycoside Kaempferol Luteolin Apigenin Alkaline Hydrolysis 
This is a preview of subscription content, log in to check access.

References

  1. 1.
    T. A. Geissman, The Chemistry of Flavonoid Compounds, Pergamon Press, N. Y., 1962.Google Scholar
  2. 2.
    A. R. Trim, in. K. Paech and M. Tracey, Modern Methoden der Pflanzenanalyse, Springer Verlag, 2, 295, 1955.Google Scholar
  3. 3.
    R. Paris, Pharm. Acta Helv., 37, 336, 1962.PubMedGoogle Scholar
  4. 4.
    V. I. Litvinenko, Rast. res., no. 4, 531, 1966.Google Scholar
  5. 5.
    E. V. Gella, G. V. Makarova, Yu. G. Borisyuk, and V. I. Litvinenko, Farm. zh., no. 3, 58, 1966.Google Scholar
  6. 6.
    E. Ballou, Adv. Carbohydr., Chem., 9, 59, 1954.Google Scholar
  7. 7.
    R. M. Horowitz and B. Gentili, Tetrah., 19, 773, 1963.CrossRefGoogle Scholar
  8. 8.
    T. A. Sergienko, L. S. Kazarnovskii, and V. I. Litvinenko, KhPS [Chemistry of Natural Compounds], 2, 166, 1966.Google Scholar
  9. 9.
    C. M. McCloskey and G. H. Coleman, J. Org. Chem., 10, 184, 1945.CrossRefGoogle Scholar

Copyright information

© Consultants Bareau 1972

Authors and Affiliations

  • V. I. Litvinenko
    • 1
    • 2
  • V. A. Makarov
    • 1
    • 2
  1. 1.Khar'kov Chemical and Pharmaceutical Scientific-Research InstituteUSSR
  2. 2.Pyatigorsk Pharmaceutical InstituteUSSR

Personalised recommendations

Cite article

Buy options