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STUDIES ON GLYCOSIDES ⅤⅢ.TOTAL SYNTHESIS OF NEW ALKALOID GLYCOSIDES FROM SELAGINELLA DOEDERIENII
作者姓名:Zhan Jiang LI  Cheng Fang YU  Meng Shen CAI
作者单位:Department of Organic Chemistry School of Pharmaceutical Sciences Beijing Medical University Beijing 100083
摘    要:Two new alkaloids,hordenine-O- -L-rhamnopyranoside(Ⅰ)and hordenine-0-(6′-trans-cinnamoyl)-4′-O-β-D-glucopyranosyl- -L-rhamnopyranoside(Ⅲ)isolated from Selaginella doederleinii have been synthesized the first time.A new method,in which trifluoroacetoxyl group was used both as a good leavinggroup and a protecting group for synthesis of O-glycosides with high stereo-selectivity was reported.


STUDIES ON GLYCOSIDES Ⅷ.TOTAL SYNTHESIS OF NEW ALKALOID GLYCOSIDES FROM SELAGINELLA DOEDERIENⅡ
Zhan Jiang LI,Cheng Fang YU,Meng Shen CAI.STUDIES ON GLYCOSIDES Ⅷ.TOTAL SYNTHESIS OF NEW ALKALOID GLYCOSIDES FROM SELAGINELLA DOEDERIENⅡ[J].Chinese Chemical Letters,1990,1(3):213-214.
Authors:Zhan Jiang LI  Cheng Fang YU  Meng Shen CAI
Institution:Department of Organic Chemistry School of Pharmaceutical Sciences Beijing Medical University Beijing 100083
Abstract:Two new alkaloids, hordenine-O-α-L-rhamnopyranoside(Ⅰ)and hordenine-0-(6"-trans-cinnamoyl)-4'-O-β-D-glucopyranosyl-α-L-rhamnopyranoside (Ⅲ) isolated from Selaginella doederleinii have been synthesized the first time.A new method, in which trifluoroacetoxyl group was used both as a good leaving group and a protecting group for synthesis of O-glycosides with high stereo-selectivity was reported.
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