Enantioselective total syntheses of (-)-taiwaniaquinone H and (-)-taiwaniaquinol B by iridium-catalyzed borylation and palladium-catalyzed asymmetric α-arylation

Journal of the American Chemical Society

Volumn 133, Issue 7, 2011, Pages 2088-2091

  Liao, Xuebin ^a   Stanley, Levi M ^a   Hartwig, John F ^a  

^a UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARYL BROMIDES; ARYLATIONS; BENZYLIC; BORYLATION; CARBONYL GROUPS; ENANTIOSELECTIVE TOTAL SYNTHESIS; LEWIS ACID; STEREOGENIC CENTERS;

AROMATIC COMPOUNDS; BROMINE COMPOUNDS; IRIDIUM; KETONES;

CATALYSIS;

CARBON; CARBONYL DERIVATIVE; HYDROGEN; IRIDIUM; KETONE; LEWIS ACID; PALLADIUM; QUINOLINE DERIVATIVE; TAIWANIAQUINOL B; TAIWANIAQUINOL H; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; BORYLATION; CATALYSIS; CHEMICAL BOND; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; HALOGENATION; SYNTHESIS;

BORON COMPOUNDS; CATALYSIS; DITERPENES; IRIDIUM; MOLECULAR STRUCTURE; PALLADIUM; STEREOISOMERISM;

EID: 79951827431     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja110215b     Document Type: Article

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