Skip to main content
Log in

Triterpenoid saponins

Communication 7. Monosaccharide composition and size of the carbohydrate part of gypsoside

  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    Fully methylated gypsoside was prepared, and in the hydrolyzate of this, eight methylated sugars were found by paper chromatography.

  2. 2.

    The gypsoside molecule contains one residue each of glucose, galactose, arabinose, rhamnose, fucose, and glucuronic acid together with two or three xylose residues.

  3. 3.

    A study of the carbohydrate chain of gypsoside indicates that galactose, xylose, and arabinose probably occupy terminal positions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature cited

  1. A. Ya. Khorlin, Yu. S. Ovodov, and N. K. Kochetkov, Zh. obshch. khimii,32 782 (1962).

    Google Scholar 

  2. N. K. Kochetkov and A. Ya. Khorlin, Dokl. AN SSSR150, 89 (1963).

    Google Scholar 

  3. R. Signer, Liebigs Ann. Chem.478, 246 (1930).

    Google Scholar 

  4. E. P. Clark, Industr. and Engng Chem., Anal Education13, 820 (1941).

    Google Scholar 

  5. H. O. Bouveng and B. Lindberg, Advances Carbohydr. Chem.15, 54 (1960).

    Google Scholar 

  6. W. S. Denham and H. Woodhouse, J. Chem. Soc.103, 1735 (1913).

    Google Scholar 

  7. W. N. Haworth, J. Chem. Soc.121, 1060 (1922).

    Google Scholar 

  8. W. N. Haworth, J. Chem. Soc.107, 13, (1915).

    Google Scholar 

  9. W. N. Haworth and G. C. Leitch, J. Chem. Soc.113, 188 (1918).

    Google Scholar 

  10. H. A. Hampton, W. N. Haworth, and E. L. Hirst, J. Chem. Soc. 1929, 1739.

  11. W. N. Haworth, E. L. Hirst, L. N. Owen, S. Peat, and F. J. Averill, J. Chem. Soc. 1939, 1885.

  12. R. Kuhn, H. Baer, and A. Seeliger, Liebigs Ann. Chem.611, 236 (1958).

    Google Scholar 

  13. R. Kuhn, et al., Angew. Chem.72, 805 (1960).

    Google Scholar 

  14. R. Kuhn and H. Trischman, J. Low, Angew. Chem.67, 32 (1955).

    Google Scholar 

  15. R. Kuhn and H. Baer, Ber.88, 1537 (1955).

    Google Scholar 

  16. E. Pascu and S. M. Trister, J. Amer. Chem. Soc.61, 2442 (1939).

    Google Scholar 

  17. H..Bredereck, G. Hageloch, and E. Hambsch, Ber.87, 35 (1954).

    Google Scholar 

  18. H. Bredereck and E. Hambsch, Ber.87, 38 (1954).

    Google Scholar 

  19. T. Purdie and J. C. Irvine, J. Chem. Soc.83, 1021 (1903).

    Google Scholar 

  20. E. L. Hirst and J. K. N. Jones, J. Chem. Soc. 1659 (1949).

  21. L. Hough, J. K. N. Jones, and W. H. Wadman, J. Chem. Soc. 1702 (1950).

  22. N. Kochetkov, A. Ya. Khorlin, and V. E. Vas'kovskii, Izv. AN SSSR. Otd. khim. n., 1963, 1398, 1409.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kochetkov, N.K., Khorlin, A.Y. & Ovodov, Y.S. Triterpenoid saponins. Russ Chem Bull 13, 71–76 (1964). https://doi.org/10.1007/BF01179570

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01179570

Keywords

Navigation