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期刊论文

Synthesis of bidesmosidic dihydrodiosgenin saponins bearing a 3-O-b-chacotriosyl moiety

管华诗Yichun Zhanga Yingxia Lia* Shilei Zhua Huashi Guana Feng Linb and Biao Yub*

Carbohydrate Research 339(2004)1753-1759,-0001,():

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摘要/描述

3-O-b-Chacotriosyl-26-O-b-D-glucopyranosyl-(25R)-furost-5-en (1), a mimic of the antitumor active proto-dioscin, was concisely synthesized from diosgenin in a linear nine steps and in 17% overall yield. Its congeners with a a-L-rhamnopyranosyl, blactosyl, or without a substituent at the 26-OH (13-15) were also prepared. Compound 1, as well as 13-15, did not show any inhibition against tumor cells, implying that proto-dioscin might be also inactive, but readily converted into the antitumor active dioscin.

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