Abstract
A synthetic scheme was proposed for the glycoside rosavin that includes a one-step glycosylation of cinnamyl alcohol with a disaccharide. The structure of the product was confirmed by PMR and 13C NMR spectroscopy.
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V. A. Kurkin and G. G. Zapesochnaya, Khim.-Farm. Zh., 20, No. 10, 1231 (1986).
State Pharmacopeia [in Russian], Meditsina, Moscow (1990).
V. A. Kurkin and L. G. Bondarenko, Khim.-Farm. Zh., No. 4, 47 (1995).
G. G. Zapesochnaya, V. A. Kurkin, V. A. Kir’yanov, and L. T. Bondarenko, in: Chemical and Medical—Biological Evaluation of New Phytopreparations: A Collection of Scientific Works [in Russian], Moscow (1989), p. 3.
A. F. Bochkov, S. A. Afanas’ev, and V. V. Zaikov, Formation and Breaking of Glycoside Bonds [in Russian], Nauka, Moscow (1978), p. 24.
V. A. Kurkin, Phenylpropanoids, Promising Natural Biologically Active Compounds [in Russian], Samara (1996).
Yu. A. Zhdanov, Practicum on Carbohydrate Chemistry [in Russian], Vysshaya Shkola, Moscow (1973).
L. F. Tietze and T. Eicher, Preparative Organic Chemistry [translated from Ger.], Mir, Moscow (1999).
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Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 323–324, July–August, 2006.
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Patov, S.A., Punegov, V.V. & Kuchin, A.V. Synthesis of the Rhodiola rosea glycoside rosavin. Chem Nat Compd 42, 397–399 (2006). https://doi.org/10.1007/s10600-006-0165-8
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DOI: https://doi.org/10.1007/s10600-006-0165-8