Reversal of the regiochemistry in the rhodium-catalyzed [4+3] cycloaddition between vinyldiazoacetates and dienes

Angewandte Chemie - International Edition

Volumn 53, Issue 48, 2014, Pages 13083-13087

  Guzmán, Pablo E ^a   Lian, Yajing ^a   Davies, Huw M L ^a  

^a EMORY UNIVERSITY   (United States)

Author keywords

Carbenoids; Cycloaddition; Diazo compounds; Rhodium; Synthetic methods

Indexed keywords

CYCLOADDITION; OLEFINS; RHODIUM;

CARBENOIDS; CYCLOPROPANATION; DIAZO COMPOUNDS; ENANTIOSELECTIVE; REARRANGEMENT REACTIONS; REGIOCHEMISTRY; RHODIUM-CATALYZED; SYNTHETIC METHODS;

RHODIUM COMPOUNDS;

ACETIC ACID DERIVATIVE; ALKADIENE; RHODIUM;

CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLOADDITION; STEREOISOMERISM;

ACETATES; ALKADIENES; CATALYSIS; CYCLOADDITION REACTION; MOLECULAR STRUCTURE; RHODIUM; STEREOISOMERISM;

EID: 84915746245     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201406440     Document Type: Article

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