Diastereo- and enantioselective construction of 3,3′-pyrrolidinyldispirooxindole framework via catalytic asymmetric 1,3-Dipolar cycloadditions

Journal of Organic Chemistry

Volumn 80, Issue 11, 2015, Pages 5737-5744

  Dai, Wei ^a   Jiang, Xiao Li ^a   Wu, Qiong ^b   Shi, Feng ^a   Tu, Shu Jiang ^a  

^a JIANGSU NORMAL UNIVERSITY   (China)

^b XUZHOU INSTITUTE OF TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

SCAFFOLDS;

1 ,3-DIPOLAR CYCLOADDITIONS; AZOMETHINE YLIDES; CATALYTIC ENANTIOSELECTIVE CONSTRUCTION; DIASTEREO- AND ENANTIOSELECTIVITY; ENANTIOSELECTIVE CONSTRUCTION; METHYLENEINDOLINONES; STEREOGENIC CENTERS; STRUCTURAL COMPLEXITY;

ENANTIOSELECTIVITY;

AZOMETHINE YLIDE; HYDROGEN; INDOLE DERIVATIVE; ISATIN DERIVATIVE; MOLECULAR SCAFFOLD; PYRROLIDINE DERIVATIVE; 3,3'-PYRROLIDINYLDISPIROOXINDOLE; ISATIN; SPIRO COMPOUND;

ARTICLE; ASYMMETRIC CATALYSIS; CATALYST; COLUMN CHROMATOGRAPHY; CRYSTAL; CYCLOADDITION; DIASTEREOISOMER; DIPOLE; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROGEN BOND; MICHAEL ADDITION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME; STEREOCHEMISTRY; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; CYCLOADDITION REACTION; INDOLES; ISATIN; MOLECULAR STRUCTURE; PYRROLIDINES; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84930678461     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.5b00708     Document Type: Article

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