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
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出版日期 | 2011 |
卷号 | 47期号:23页码:6644-6646 |
ISSN号 | 1359-7345 |
DOI | 10.1039/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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