Rhodium-catalyzed Michael addition of arylboronic acids to 3-alkylenyloxindoles: asymmetric synthesis of functionalized oxindoles
文献类型:期刊论文
| 作者 | Zhang, Xiangyang ; Chen, Guihua ; Cao, Peng ; Liu, Jibing ; Liao, Jian |
| 刊名 | TETRAHEDRON LETTERS
![]() |
| 出版日期 | 2012 |
| 卷号 | 53期号:4页码:438-441 |
| 关键词 | 3-Alkylenyoxindoles Functionalized oxindoles Arylboronic acids Michael addition |
| ISSN号 | 0040-4039 |
| 产权排序 | 1 |
| 通讯作者 | Liao, J (reprint author), Chinese Acad Sci, Nat Prod Res Ctr, Chengdu Inst Biol, Chengdu 610041, Peoples R China. |
| 英文摘要 | The rhodium-catalyzed diastereo- and enantioselective Michael addition of arylboronic acids to 3-alkyl-enyloxindoles has been developed with (R)-binap as a ligand. A wide variety of the desired functionalized oxindoles are smoothly obtained in high yields (up to 99%) with high enantioselectivities (up to 92% ee) and good diastereoselectivities (up to 82:18). (C) 2011 Elsevier Ltd. All rights reserved. |
| 学科主题 | Chemistry |
| 收录类别 | SCI |
| 资助信息 | NSFC [21072186, 20872139]; West Light Foundation of Chinese Academy of Sciences; National Basic Research Program of China (973 Program) [2010CB833300]; Chengdu Institute of Biology, Chinese Academy of Sciences [Y0B1051100] |
| 语种 | 英语 |
| WOS记录号 | WOS:000300027200019 |
| 公开日期 | 2013-07-03 |
| 源URL | [http://210.75.237.14/handle/351003/23916] ![]() |
| 专题 | 成都生物研究所_天然产物研究 |
| 推荐引用方式 GB/T 7714 | Zhang, Xiangyang,Chen, Guihua,Cao, Peng,et al. Rhodium-catalyzed Michael addition of arylboronic acids to 3-alkylenyloxindoles: asymmetric synthesis of functionalized oxindoles[J]. TETRAHEDRON LETTERS,2012,53(4):438-441. |
| APA | Zhang, Xiangyang,Chen, Guihua,Cao, Peng,Liu, Jibing,&Liao, Jian.(2012).Rhodium-catalyzed Michael addition of arylboronic acids to 3-alkylenyloxindoles: asymmetric synthesis of functionalized oxindoles.TETRAHEDRON LETTERS,53(4),438-441. |
| MLA | Zhang, Xiangyang,et al."Rhodium-catalyzed Michael addition of arylboronic acids to 3-alkylenyloxindoles: asymmetric synthesis of functionalized oxindoles".TETRAHEDRON LETTERS 53.4(2012):438-441. |
入库方式: OAI收割
来源:成都生物研究所
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。

