Synthesis of six-membered spirocyclic oxindoles with five consecutive stereocenters in an asymmetric organocatalytic one-pot michael/michael/aldol addition sequence

Journal of Organic Chemistry

Volumn 78, Issue 7, 2013, Pages 2897-2907

  Zhou, Bing ^a   Yang, Yaxi ^a   Shi, Jingjing ^a   Luo, Zhi ^a   Li, Yuanchao ^a  

^a SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BI-FUNCTIONAL; DIASTEREOMERS; ONE-POT PROTOCOL; ONE-POT SYNTHESIS; ORGANOCATALYSTS; ORGANOCATALYTIC; REACTION CATALYZED; STEREOCENTERS;

THIOUREAS;

ADDITION REACTIONS;

DIPHENYLPROLINOL SILYL ETHER; NITROALKANE; OXINDOLE; TOLUENE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CATALYSIS; CHEMICAL MODIFICATION; COLUMN CHROMATOGRAPHY; CONTROLLED STUDY; DIASTEREOISOMER; ELECTRON TRANSPORT; ENANTIOSELECTIVITY; MICHAEL ADDITION; ONE POT SYNTHESIS; ROOM TEMPERATURE;

CATALYSIS; INDOLES; MOLECULAR STRUCTURE; ORGANIC CHEMICALS; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84875966355     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo302655u     Document Type: Article

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