中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes

文献类型:期刊论文

作者Xing, Junwei ; Chen, Guihua ; Cao, Peng ; Liao, Jian
刊名EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
出版日期2012
期号6页码:1230-1236
关键词Synthetic methods Asymmetric synthesis Homogeneous catalysis Rhodium Heterocycles
ISSN号1434-193X
产权排序2
通讯作者Liao, J (reprint author), Chinese Acad Sci, Chengdu Inst Organ Chem, Key Lab Asymmetr Synth & Chirotechnol Sichuan Pro, Chengdu 610041, Peoples R China.
英文摘要Indolylnitroethanes and their derivatives are key intermediates to many bioactive structures. Most approaches to access chiral indolylnitroethanes involve organocatalyzed or metal-catalyzed asymmetric FriedelCrafts reaction of indoles with nitroalkenes. We have developed an efficient approach to optically pure a-aryl-3-indolylnitroethanes through rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids to indolylnitroalkenes. Excellent yields (up to 99?%) and enantiomeric excesses (up to 99?% ee) of chiral indolylnitroethanes were achieved under mild conditions.
学科主题Chemistry
收录类别SCI
资助信息National Natural Science Foundation of China (NSFC) [21072186, 20872139]; West Light Foundation of CAS; National Basic Research Program of China (973 Program) [2010CB833300]; Chengdu Institute of Biology, CAS [Y0B1051100]
语种英语
WOS记录号WOS:000300499000025
公开日期2013-07-03
源URL[http://210.75.237.14/handle/351003/23915]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Xing, Junwei,Chen, Guihua,Cao, Peng,et al. Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes[J]. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY,2012(6):1230-1236.
APA Xing, Junwei,Chen, Guihua,Cao, Peng,&Liao, Jian.(2012).Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes.EUROPEAN JOURNAL OF ORGANIC CHEMISTRY(6),1230-1236.
MLA Xing, Junwei,et al."Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes".EUROPEAN JOURNAL OF ORGANIC CHEMISTRY .6(2012):1230-1236.

入库方式: OAI收割

来源:成都生物研究所

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