中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly enantioselective Michael addition of 2-oxindoles to vinyl selenone in RTILs catalyzed by a Cinchona alkaloid-based thiourea

文献类型:期刊论文

作者Zhang, Tao1,2; Cheng, Liang1; Hameed, Shahid1,3; Liu, Li1; Wang, Dong1; Chen, Yong-Jun1
刊名CHEMICAL COMMUNICATIONS
出版日期2011
卷号47期号:23页码:6644-6646
ISSN号1359-7345
DOI10.1039/c1cc10880h
英文摘要A highly enantioselective Michael addition of 2-oxindoles (1) to vinyl selenone (2) in RTILs catalyzed by a Cinchona alkaloid-based thiourea has been developed in high yields (80-91%) with excellent enantioselectivities (up to 95% ee).
语种英语
WOS记录号WOS:000291113000037
出版者ROYAL SOC CHEMISTRY
源URL[http://ir.iccas.ac.cn/handle/121111/71567]  
专题中国科学院化学研究所
通讯作者Liu, Li
作者单位1.Chinese Acad Sci, Beijing Natl Lab Mol Sci BNLMS, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
3.Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan
推荐引用方式
GB/T 7714
Zhang, Tao,Cheng, Liang,Hameed, Shahid,et al. Highly enantioselective Michael addition of 2-oxindoles to vinyl selenone in RTILs catalyzed by a Cinchona alkaloid-based thiourea[J]. CHEMICAL COMMUNICATIONS,2011,47(23):6644-6646.
APA Zhang, Tao,Cheng, Liang,Hameed, Shahid,Liu, Li,Wang, Dong,&Chen, Yong-Jun.(2011).Highly enantioselective Michael addition of 2-oxindoles to vinyl selenone in RTILs catalyzed by a Cinchona alkaloid-based thiourea.CHEMICAL COMMUNICATIONS,47(23),6644-6646.
MLA Zhang, Tao,et al."Highly enantioselective Michael addition of 2-oxindoles to vinyl selenone in RTILs catalyzed by a Cinchona alkaloid-based thiourea".CHEMICAL COMMUNICATIONS 47.23(2011):6644-6646.

入库方式: OAI收割

来源:化学研究所

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