Organocatalytic asymmetric sulfa-michael/michael addition reactions: A strategy for the synthesis of highly substituted chromans with a quaternary stereocenter

Angewandte Chemie - International Edition

Volumn 49, Issue 45, 2010, Pages 8379-8383

  Wang, Xu Fan ^a   Hua, Qiu Lin ^a   Cheng, Ying ^a   An, Xiao Lei ^a   Yang, Qing Qing ^a   Chen, Jia Rong ^a   Xiao, Wen Jing ^a  

^a CENTRAL CHINA NORMAL UNIVERSITY   (China)

Author keywords

Heterocycles; Hydrogen bonds; Michael addition; Organocatalysis; Synthetic methods

Indexed keywords

BI-FUNCTIONAL CATALYSTS; CHROMAN DERIVATIVES; DIASTEREO-SELECTIVITY; ENANTIOMERIC EXCESS; EXPERIMENTAL PROCEDURE; HETEROCYCLES; HIGH YIELD; MICHAEL ADDITIONS; ORGANOCATALYSIS; ORGANOCATALYTIC; QUATERNARY STEREOCENTERS; SYNTHETIC METHODS;

ADDITION REACTIONS; CATALYSIS; COMPLEXATION; HYDROGEN; RATE CONSTANTS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

HYDROGEN BONDS;

ALKENE; CHROMAN DERIVATIVE; HETEROCYCLIC COMPOUND; THIOL DERIVATIVE;

ARTICLE; CATALYSIS; CHEMISTRY; CONFORMATION; HYDROGEN BOND; STEREOISOMERISM;

ALKENES; CATALYSIS; CHROMANS; HETEROCYCLIC COMPOUNDS; HYDROGEN BONDING; MOLECULAR CONFORMATION; STEREOISOMERISM; SULFHYDRYL COMPOUNDS;

EID: 78149445810     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201004534     Document Type: Article

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