ICCAS OpenIR
Highly enantioselective Michael addition of 2-oxindoles to vinyl selenone in RTILs catalyzed by a Cinchona alkaloid-based thiourea
Zhang, Tao1,2; Cheng, Liang1; Hameed, Shahid1,3; Liu, Li1; Wang, Dong1; Chen, Yong-Jun1
2011
Source PublicationCHEMICAL COMMUNICATIONS
ISSN1359-7345
Volume47Issue:23Pages:6644-6646
AbstractA 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).
DOI10.1039/c1cc10880h
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000291113000037
PublisherROYAL SOC CHEMISTRY
Citation statistics
Cited Times:44[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/71568
Collection中国科学院化学研究所
Corresponding AuthorLiu, Li
Affiliation1.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
Recommended Citation
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.
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