Reversible C-C bond activation enables stereocontrol in Rh-catalyzed carbonylative cycloadditions of aminocyclopropanes

Journal of the American Chemical Society

Volumn 137, Issue 1, 2015, Pages 463-468

  Shaw, Megan H ^a   McCreanor, Niall G ^a   Whittingham, William G ^b   Bower, John F ^a  

^a UNIVERSITY OF BRISTOL   (United Kingdom)

^b JEALOTT S HILL INTERNATIONAL RESEARCH CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CYCLOADDITION; HYDROCARBONS; RHODIUM; SCAFFOLDS;

ALKENE INSERTION; C-C BOND ACTIVATION; CATALYST SYSTEM; CONTROL STRATEGIES; DIASTEREO-SELECTIVITY; MECHANISTIC STUDIES; N-HETEROCYCLIC; REGIO-SELECTIVE;

RHODIUM COMPOUNDS;

ALKENE; CYCLOPENTANONE DERIVATIVE; CYCLOPROPANECARBOXYLIC ACID DERIVATIVE; CYCLOPROPANE DERIVATIVE; HETEROCYCLIC COMPOUND; RHODIUM;

ARTICLE; CATALYSIS; CHEMICAL BOND; CYCLIZATION; CYCLOADDITION; DIASTEREOISOMER; STEREOCHEMISTRY; SYNTHESIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM;

ALKENES; CATALYSIS; CYCLIZATION; CYCLOPROPANES; HETEROCYCLIC COMPOUNDS; MOLECULAR STRUCTURE; RHODIUM; STEREOISOMERISM;

EID: 84921064474     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja511335v     Document Type: Article

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