trans-directing ability of the amide group: Enabling the enantiocontrol in the synthesis of 1,1-dicarboxy cyclopropanes. Reaction development, scope, and synthetic applications

Journal of Organic Chemistry

Volumn 74, Issue 23, 2009, Pages 8939-8955

  Marcoux, David ^a   Goudreau, Sébastien R ^a   Charette, André B ^a  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE GROUPS; CHEMICAL EQUATIONS; CYCLOPROPANATION; CYCLOPROPANATION REACTION; CYCLOPROPANE DERIVATIVE; DIESTERS; ENANTIOCONTROL; ENANTIOSELECTIVE FORMATION; EROGORGIAENE; FORMAL SYNTHESIS; FUNCTIONAL GROUP TRANSFORMATIONS; POTENTIAL UTILITY; STEREO-SELECTIVE; STEREOSELECTIVE SYNTHESIS; SYNTHETIC APPLICATION;

AMIDES; FLUORINE CONTAINING POLYMERS; FUNCTIONAL GROUPS; OLEFINS; RHODIUM; STEREOSELECTIVITY;

PROPANE;

ALKENE; ALKENE DERIVATIVE; AMIDE; CURCUMIN; CYCLOPROPANE DERIVATIVE; ESTER DERIVATIVE; RHODIUM DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CYCLOPROPANATION; ENANTIOSELECTIVITY; METHODOLOGY; STEREOCHEMISTRY; SYNTHESIS;

EID: 72249098560     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo902066y     Document Type: Article

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