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TWONEW TRITERPENOID SAPONINS,ASTERBATANOSIDE H AND I,FROM ASTER BATANGENSIS 被引量:1
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作者 Shao, Y zhou, bn +1 位作者 Lin, LZ Cordell, GA 《Chinese Chemical Letters》 SCIE CAS CSCD 1995年第2期105-108,共4页
Two new triterpenoid saponins named asterbatanoside H and I have been isolated from the roots of Aster batsngensis and their structures elucidated as 3-O-β-D-glucopyranosyl-(1→3) β-D-glucopyranosyl-bayogenin-28-O-... Two new triterpenoid saponins named asterbatanoside H and I have been isolated from the roots of Aster batsngensis and their structures elucidated as 3-O-β-D-glucopyranosyl-(1→3) β-D-glucopyranosyl-bayogenin-28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosy-(1→6) and 3-O-β-D-glucopyranosyl-(1→3)-β-D-glucopyranosyl-23-O-acetyl-bayogenin-28-O-β-D-glucopyranosyl-(1→6) β-D-glucopyranoside, respectively, by means of spectral and chemical data. 展开更多
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THE STRUCTURE OF ASTERBATANOSIDE J FROM ASTER BATANGENSIS 被引量:1
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作者 Shao, Y zhou, bn +1 位作者 Lin, LZ Cordell, GA 《Chinese Chemical Letters》 SCIE CAS CSCD 1995年第3期221-224,共4页
A new medicagenic acid saponin named asterbatanoside J was isolated from the roots of Aster batangensis. On the basis of chemical and spectral studies especially 2D NMR including COSY, HETCOR, HOHAHA, ROESY and HMBC t... A new medicagenic acid saponin named asterbatanoside J was isolated from the roots of Aster batangensis. On the basis of chemical and spectral studies especially 2D NMR including COSY, HETCOR, HOHAHA, ROESY and HMBC techniques, its structure has been established as 3-O-beta -D-glucopyranosyl-(1 -->6)-beta -D-glucopyranosyl-2 beta ,3 beta -dihydroxy-olean-12-en-23 alpha ,28-dioic acid-28-O-alpha -L-arabinopyranosyl-(1 -->3)-alpha -L-rhamnopyranosyl-(1 -->2)-beta -D-fucopyranoside. 展开更多
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