Diastereo- and enantioselective [3 + 2] cycloaddition reaction of Morita-Baylis-Hillman carbonates of isatins with N -phenylmaleimide catalyzed by Me-DuPhos

Journal of Organic Chemistry

Volumn 77, Issue 8, 2012, Pages 4143-4147

  Wang, Yan ^a,b   Liu, Li ^a   Zhang, Tao ^a,b   Zhong, Neng Jun ^a,b   Wang, Dong ^a   Chen, Yong Jun ^a  

^a INSTITUTE OF CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CHIRAL CENTERS; CYCLOADDITION REACTION; ENANTIOSELECTIVE; ENANTIOSELECTIVIES; N-PHENYLMALEIMIDE; ONE STEP; PHENYLMALEIMIDE;

CARBONATES; CYCLOADDITION; RATE CONSTANTS;

CATALYSIS;

CARBONIC ACID DERIVATIVE; ISATIN DERIVATIVE; MALEIMIDE DERIVATIVE; OXINDOLE; PHOSPHINE DERIVATIVE;

ARTICLE; BAYLIS HILLMAN REACTION; CATALYSIS; CHEMICAL REACTION; CHIRALITY; CYCLOADDITION; ENANTIOSELECTIVITY; MORTIA REACTION; STEREOCHEMISTRY;

CARBONATES; CATALYSIS; CYCLIZATION; ISATIN; MALEIMIDES; MOLECULAR STRUCTURE; PHOSPHINES; STEREOISOMERISM;

EID: 84860211253     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3002535     Document Type: Article

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