Enantioselective synthesis of quaternary 3-aminooxindoles via organocatalytic asymmetric michael addition of 3-monosubstituted 3-aminooxindoles to nitroolefins

Journal of Organic Chemistry

Volumn 78, Issue 17, 2013, Pages 8833-8839

  Cui, Bao Dong ^a,c   Han, Wen Yong ^a,c   Wu, Zhi Jun ^b   Zhang, Xiao Mei ^a   Yuan, Wei Cheng ^a  

^a CHENGDU INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b CHENGDU INSTITUTE OF BIOLOGY   (China)

^c UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BI-FUNCTIONAL; ENANTIOSELECTIVE SYNTHESIS; MICHAEL ADDITION REACTIONS; MICHAEL ADDITIONS; NITROOLEFINS; ORGANOCATALYTIC; OXINDOLES; SYNTHETIC UTILITY;

ADDITION REACTIONS; CHEMICAL COMPOUNDS; ENANTIOSELECTIVITY;

SELECTIVE CATALYTIC REDUCTION;

1 METHYL 5' PHENYL 5',6' DIHYDRO 1' H SPIRO [INDOLINE 3,4' PYRIMIDINE] 2,2' 3H DIONE; 3 AMINOOXINDOLE; ALKENE; ETHYL 1 ETHYL 3 2 NITRO 1 PHENYLETHYL) 2 OXOINDOLIN 3 YL CARBAMATE; OXINDOLE; TERTIARY AMINE; THIOUREA; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; DRUG STRUCTURE; ENANTIOSELECTIVITY; MICHAEL ADDITION; PROTEIN QUATERNARY STRUCTURE; PROTEIN TERTIARY STRUCTURE;

ALKENES; AMINES; CATALYSIS; INDOLES; MOLECULAR STRUCTURE; NITRO COMPOUNDS; STEREOISOMERISM;

EID: 84883761024     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo401154b     Document Type: Article

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