中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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

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