The asymmetric total synthesis of (+)-salvianolic acid A | |
Zheng, Yong; Song, Wei-Bin; Xuan, Li-Jiang | |
刊名 | TETRAHEDRON |
2016-08-18 | |
卷号 | 72期号:33页码:5047-5050 |
关键词 | Asymmetric addition Aryl metal reagents Phenyl-D-lactic acid C-H activation Salvianolic acid A |
ISSN号 | 0040-4020 |
DOI | 10.1016/j.tet.2016.05.070 |
文献子类 | Article |
英文摘要 | An asymmetric synthesis of (+)-salvianolic acid A with cardioprotective properties, has been accomplished in a convergent manner in eight steps and 10.6% overall yield. This synthesis features an asymmetric addition of organometallics to optically pure 2,3-epoxypropionate in the presence of BF3 center dot Et2O, Ru(III)-catalyzed directed C-H olefination, and I-2-catalyzed isomerization reaction. (C) 2016 Elsevier Ltd. All rights reserved. |
资助项目 | National Science & Technology Major Project 'Key New Drug Creation and Manufacturing Program', China[SIMM1601ZZ-03] ; China Postdoctoral Science Foundation[2014M550257] |
WOS关键词 | SALVIANOLIC ACID ; (+)-LITHOSPERMIC ACID ; BIOLOGICAL EVALUATION ; ENANTIOSELECTIVE REDUCTION ; ROUTE ; DERIVATIVES ; ACTIVATION ; INHIBITOR ; KETONES ; ESTERS |
WOS研究方向 | Chemistry |
语种 | 英语 |
出版者 | PERGAMON-ELSEVIER SCIENCE LTD |
WOS记录号 | WOS:000381170600006 |
内容类型 | 期刊论文 |
源URL | [http://119.78.100.183/handle/2S10ELR8/275925] |
专题 | 上海中药现代化研究中心 中科院受体结构与功能重点实验室 新药研究国家重点实验室 |
通讯作者 | Xuan, Li-Jiang |
作者单位 | Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, 501 Haike Rd,Zhangjiang Hitech Pk, Shanghai 201203, Peoples R China |
推荐引用方式 GB/T 7714 | Zheng, Yong,Song, Wei-Bin,Xuan, Li-Jiang. The asymmetric total synthesis of (+)-salvianolic acid A[J]. TETRAHEDRON,2016,72(33):5047-5050. |
APA | Zheng, Yong,Song, Wei-Bin,&Xuan, Li-Jiang.(2016).The asymmetric total synthesis of (+)-salvianolic acid A.TETRAHEDRON,72(33),5047-5050. |
MLA | Zheng, Yong,et al."The asymmetric total synthesis of (+)-salvianolic acid A".TETRAHEDRON 72.33(2016):5047-5050. |
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