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V. N. Luchanskaya E. S. Kondratenko N. K. Abubakirov 《Chemistry of Natural Compounds》1973,7(4):409-411
Summary The structure of trichoside B — a gypsogenin tetraoside fromGypsophila trichotoma Wend. — has been established. The glycosidic carbohydrate chain is O--D-glucopyranosyl-(1 3)-O--D-glucuronopyranosyl and the acyloside chain is O--D-glucopyranosyl-(1 4)-O--D-galactopyranosyl.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 431–434, July–August, 1971. 相似文献
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Luchanskaya V. N. Kondratenko E. S. Abubakirov N. K. 《Chemistry of Natural Compounds》1972,8(1):63-65
Chemistry of Natural Compounds - The structure of the glycosidic carbohydrate chain and the partial structure of the acyloside chain of trichoside D — a new triterpene glycoside... 相似文献
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V. N. Luchanskaya E. S. Kondratenko T. T. Gorovits N. K. Abubakirov 《Chemistry of Natural Compounds》1973,7(2):142-144
Summary The structure of trichoside A — a gypsogenin trioside fromGypsophylla trichotoma Wend. — has been established. The O-glycosidic moiety is the O--D-glucopyranosyl-(1 3)-O--D-glucopyranoside grouping and the O-acyl moiety is D-galactose.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodynkh Soedinenii, Vol. 7, No. 2, pp. 151–153, March, 1971. 相似文献
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V. N. Luchanskaya E. S. Kondratenko N. K. Abubakirov 《Chemistry of Natural Compounds》1974,8(1):63-65
Summary The structure of the glycosidic carbohydrate chain and the partial structure of the acyloside chain of trichoside D — a new triterpene glycoside fromGypsophila trichotoma — have been established.Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 69–72, January–February, 1972. 相似文献
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Chemistry of Natural Compounds - 相似文献
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V. Ya. Chirva P. K. Kintya V. A. Sosnovskii P. E. Krivenchuk N. Ya. Zykova 《Chemistry of Natural Compounds》1970,6(2):213-215
Conclusions The structure of two triterpone glycosides fromSapindus mukorossi Gaertn. has been established. It has been shown that sapindoside A is hederagenin 3-O--L-arabinosyl-(2 1)--L-rhamnopyranoside and sapindoside B is the 3-O--L-arabopyranosyl-(2 1)-O--L-rhamnopyranosyl-(3 1)--D-xylopyranoside. 相似文献
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A. A. Akimaliev N. Sh. Pal'yants P. K. Alimbaeva N. K. Abubakirov 《Chemistry of Natural Compounds》1979,15(5):587-591
Partial syntheses of glycosides of oleanolic acid — the 3-0-β-D-xylopyranoside (songoroside A), the 3,28-bis-0-β-D-xylopyranoside, and the 28-0-β-gentiobioside-3-0-β-D-xylopyranoside — and also the formation of 3-0-β-D-xylopyranosyloleanolic acid 13,28-lactone are described. 相似文献
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Putieva Zh. M. Mzhel'skaya L. G. Kondratenko E. S. Abubakirov N. K. 《Chemistry of Natural Compounds》1970,6(4):506-507
Chemistry of Natural Compounds - 相似文献