| 苯丙素苷Acteoside,Isoacteoside和Ligupurpuroside J的全合成 |
| |
| 引用本文： | 胡志飞,徐鹏,魏炳成,俞飚. 苯丙素苷Acteoside,Isoacteoside和Ligupurpuroside J的全合成[J]. 高等学校化学学报, 2020, 41(8): 1708-1720. DOI: 10.7503/cjcu20200266 |
| |
| 作者姓名： | 胡志飞 徐鹏 魏炳成 俞飚 |
| |
| 作者单位： | 1. 上海科技大学物质科学与技术学院, 上海 201210;2. 中国科学院上海有机化学研究所生命有机化学国家重点实验室, 上海 200032 |
| |
| 基金项目： | 国家自然科学基金（批准号：21621002）和王宽诚率先人才计划资助. |
| |
| 摘 要： | 发展了一条合成苯丙素苷类化合物的通用路线,并依据此路线完成了苯丙素苷毛蕊花糖苷(Acteoside)和异毛蕊花糖苷(Isoacteoside)的全合成及紫茎女贞苷J(Ligupurpuroside J)的首次全合成.其中的关键步骤是应用金(Ⅰ)催化的鼠李糖邻炔基苯甲酸酯给体与多羟基裸露的2-苯乙基葡萄糖苷进行区域选择性糖苷化反应,成功构建天然苯丙素苷中常见的α-(1→3)糖苷键.该合成路线减少了保护基的使用,简洁高效.
|
| 关 键 词： | 苯丙素苷 毛蕊花糖苷 异毛蕊花糖苷 紫茎女贞苷J 糖苷化反应 |
| 收稿时间： | 2020-05-13 |
Total Synthesis of Phenylpropanoid Glycosides,Acteoside, Isoacteoside and Ligupurpuroside J |
| |
| HU Zhifei,XU Peng,WEI Bingcheng,YU Biao. Total Synthesis of Phenylpropanoid Glycosides,Acteoside, Isoacteoside and Ligupurpuroside J[J]. Chemical Research In Chinese Universities, 2020, 41(8): 1708-1720. DOI: 10.7503/cjcu20200266 |
| |
| Authors: | HU Zhifei XU Peng WEI Bingcheng YU Biao |
| |
| Affiliation: | 1. School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China;2. State Key Laboratory of Bio-organic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China |
| |
| Abstract: | Phenylpropanoid glycosides(PPGs), a kind of natural glycosides with C6-C3 aromatic framework, are widely distributed in the plant kingdom. These glycosides show various medicinal properties, inclu-ding antioxidative, antibacterial, antiviral and antitumor activities. Nevertheless, because of their low content in plants, the isolation of these compounds is a formidable task, so as to retard in-depth studies of their biological activities. Thus, the development of effective approaches to the synthesis of phenylpropanoid glycosides has attracted a great attention. Since the 1990s, several syntheses have been reported, however most of these synthetic routes are lengthy due to multi-step manipulations of protecting groups, especially some of the protecting groups/deprotecting reagents are incompatible with the α,β-unsaturated ester occurring in PPGs. Here, we report a general and effective synthetic approach to PPGs. The present approach features a regioselective glycosylation of 2-phenylethyl glucoside polyols with rhamnosyl o-alkynylbenzoate donors under the catalysis of triphenyephosphinegold(Ⅰ) bis(trifluormethanesulfonye) imidate(PPh3AuNTf2, 10%-15%, molar fraction) at low temperature to furnish the key α-(1→3)-linked saccharides. Then, the 2-OH in the glucose unit was selectively protected with acetyl chloride, subsequent condensation with caffeic acid with the remaining C4-OH completed the major PPGs framework. Global removal of the acetyl and allyl groups afforded acteoside. Similar approaches were successfully applied to the synthesis of Isoacteoside and Ligupurposite J, which contained caffeic acid residue at the C6-OH of the glucose unit. The regioselective glycosylation, which avoids selective protection/deprotection of the hydroxyl groups, provides a shorter synthetic approach toward the PPGs. |
| |
| Keywords: | Phenylpropanoid glycosides Acteoside Isoacteoside Ligupurpuroside J Glycosylation |
| 本文献已被 CNKI 等数据库收录！ |
| 点击此处可从《高等学校化学学报》浏览原始摘要信息 |
|
点击此处可从《高等学校化学学报》下载全文 |
|
