Bifunctional catalyst promotes highly enantioselective bromolactonizations to generate stereogenic C-Br bonds

Journal of the American Chemical Society

Volumn 134, Issue 27, 2012, Pages 11128-11131

  Paull, Daniel H ^a   Fang, Chao ^a   Donald, James R ^a   Pansick, Andrew D ^a   Martin, Stephen F ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BI-FUNCTIONAL CATALYSTS; BROMOLACTONIZATION; CARBON-BROMINE BONDS; CYCLIZATIONS; DESYM-METRIZATION; ENANTIOSELECTIVE; HIGH ENANTIOSELECTIVITY; PENTENOIC ACID; STEREOGENIC CENTERS; UNSATURATED ACIDS;

BROMINE; CATALYSTS;

ENANTIOSELECTIVITY;

2,2' DIHYDROXY 1,1' BINAPHTHYL; 4 PENTENOIC ACID; BROMINE; CARBON; FUNCTIONAL GROUP; LACTONE DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; ENANTIOMER; ENANTIOSELECTIVITY; LACTONIZATION; SYNTHESIS;

ALKENES; BROMINE; CARBOXYLIC ACIDS; CATALYSIS; HALOGENATION; LACTONES; NAPHTHOLS; STEREOISOMERISM;

EID: 84863822060     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja305117m     Document Type: Article

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