Highly enantioselective Michael addition of 2-oxindoles to vinyl selenone in RTILs catalyzed by a Cinchona alkaloid-based thiourea

Chemical Communications

Volumn 47, Issue 23, 2011, Pages 6644-6646

  Zhang, Tao ^a,b   Cheng, Liang ^a   Hameed, Shahid ^a,c   Liu, Li ^a   Wang, Dong ^a   Chen, Yong Jun ^a  

^a INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c QUAID I AZAM UNIVERSITY   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

CINCHONA ALKALOID; IONIC LIQUID; OXINDOLE; THIOUREA; VINYL DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; MICHAEL ADDITION; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 79957993312     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c1cc10880h     Document Type: Article

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