Total synthesis of a furostan saponin, timosaponin BII
文献类型：期刊论文
| 作者 | Cheng, Shuihong ; Du, Yuguo ; Ma, Baiping ; Tan, Dawei |
| 刊名 | ORGANIC & BIOMOLECULAR CHEMISTRY
 |
| 出版日期 | 2009 |
| 卷号 | 7期号:15页码:3112-3118 |
| 中文摘要 | The natural timosaponin BII, (25S)-26-O-beta-D-glucopyranosyl-22-hydroxy-5 beta-furostane-3 beta,26-diol-3-O-beta-D-glucopyranosyl-(1 -> 2)-beta-D-galactopyranoside, isolated from the rhizomes of Anemarrhena asphodeloides Bunge (Liliaceae), has been effeciently synthesized in ten steps and 18% overall yield. The strategy of using a partially protected glycosyl donor was applied to facilitate target synthesis. The cytotoxic activities of structurally related compounds were evaluated against HL-60 human promyelocytic leukaemia cells. |
| WOS记录号 | WOS:000268033500017 |
| 源URL | [http://ir.rcees.ac.cn/handle/311016/21582]  |
| 专题 | 生态环境研究中心_环境化学与生态毒理学国家重点实验室 |
| 推荐引用方式 GB/T 7714 | Cheng, Shuihong,Du, Yuguo,Ma, Baiping,et al. Total synthesis of a furostan saponin, timosaponin BII[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2009,7(15):3112-3118. |
| APA | Cheng, Shuihong,Du, Yuguo,Ma, Baiping,&Tan, Dawei.(2009).Total synthesis of a furostan saponin, timosaponin BII.ORGANIC & BIOMOLECULAR CHEMISTRY,7(15),3112-3118. |
| MLA | Cheng, Shuihong,et al."Total synthesis of a furostan saponin, timosaponin BII".ORGANIC & BIOMOLECULAR CHEMISTRY 7.15(2009):3112-3118. |
入库方式： OAI收割
来源：生态环境研究中心
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