Abstract
The structure of taurorisde E — the predominating triterpene glycoside from the leaves of Crimean ivy,Hedera taurica Carr. has been established by1H and13C NMR spectroscopy using nuclear Overhauser effects. It is 3-O-[O-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl]hederagenin.
Article PDF
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Literature cited
G. B. Elyakov and Yu. S. Ovodov, Khim. Prior. Soedin., 697 (1972).
S. Seo, Y. Tomita, K. Tori, and Y. Yoshimura, J. Am. Chem. Soc.,100, No. 11, 3331 (1978).
P. A. J. Gorin and M. Mazurek, Carbohydr. Res.,48, No. 2, 171 (1976).
K. Bock, I. Lundt, and C. Pedersen, Tetrahedron Lett., No. 13, 1037 (1973).
H. Kizu and T. Tomimori, Chem. Pharm. Bull.,30, No. 3, 859 (1982).
Additional information
M. V. Frunze Simferopol' State University. Translated from Khimiya Prirodnykh Soedenenii, No. 3, pp. 363–366, May–June, 1987.
Rights and permissions
About this article
Cite this article
Shashkov, A.S., Grishkovets, V.I., Loloiko, A.A. et al. Triterpene glycosides ofHedera taurica I. Structure of tauroside E from the leaves ofHedera taurica . Chem Nat Compd 23, 299–302 (1987). https://doi.org/10.1007/BF00600827
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00600827