• 首页期刊简介编委会刊物订阅专栏专刊电子刊学术动态联系我们English
引用本文:孔祥文.地黄苷的全合成[J].中国现代应用药学,2014,31(4):424-429.
KONG Xiangwen.Total Synthesis of Martynoside[J].Chin J Mod Appl Pharm(中国现代应用药学),2014,31(4):424-429.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 3054次   下载 1695 本文二维码信息
码上扫一扫!
分享到: 微信 更多
地黄苷的全合成
孔祥文
杭州中美华东制药有限公司,杭州 310011
摘要:
目的 合成天然苯丙素苷地黄苷。方法 以D-葡萄糖为起始原料,经乙酰化、溴代、成醚、脱乙酰基、引入保护基和取代鼠李糖、脱亚苄基、酰化、脱除保护基等反应合成地黄苷。结果 首次完成苯丙素苷地黄苷的化学合成,其结构经1H-NMR、13C-NMR、MS和元素分析确证,并与文献数据一致。结论 合成工艺原料易得,方法可行。
关键词:  地黄苷  苯丙素苷  合成  保护基
DOI:
分类号:R284.1;R917.101
基金项目:
Total Synthesis of Martynoside
KONG Xiangwen
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd., Hangzhou 310011, China
Abstract:
OBJECTIVE To synthesis the natural phenylpropanoid glycoside, martynoside. METHODS Using D-glucose as the starting material, martynoside was successfully synthesized via acetylation, bromination, etherification, removing acetyl, introducing protective groups and substituted rhamnose, removing benzylidene, acylation, and removing protective groups. RESULTS The chemical synthesis of the phenylpropanoid glycoside martynoside was realized for the first time. Its structure was identified by 1H-NMR, 13C-NMR and MS spectroscopy, as well as by elemental analysis. CONCLUSION The starting materials are easy to get and the method is feasible.
Key words:  martynoside  phenylpropanoid glycosides  synthesis  protective groups
扫一扫关注本刊微信