An enantioselective, intermolecular α-arylation of ester enolates to form tertiary stereocenters

Journal of the American Chemical Society

Volumn 133, Issue 40, 2011, Pages 15882-15885

  Huang, Zhiyan ^a   Liu, Zheng ^a   Zhou, Jianrong ^a  

^a Nanyang Technological University   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

ARYL TRIFLATES; ARYLATIONS; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE; ENOLATES; ENOLIZATION; GRAM-SCALE SYNTHESIS; HIGH ENANTIOSELECTIVITY; MONOARYLATION; NAPROXENS; PALLADIUM CATALYST; SILYL KETENE ACETAL; TERTIARY CENTERS; TERTIARY STEREOCENTERS;

AROMATIC COMPOUNDS; CARBONYL COMPOUNDS; CATALYSTS; ESTERIFICATION; ESTERS; PALLADIUM; SYNTHESIS (CHEMICAL); TRANSITION METALS;

ENANTIOSELECTIVITY;

ESTER; KETENE DERIVATIVE; NAPROXEN; PALLADIUM; SILYL KETEN ACETAL; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CHEMICAL REACTION; ELIMINATION REACTION; ENANTIOSELECTIVITY; ENOLIZATION; HYDROLYSIS; SYNTHESIS;

ACETALS; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; CATALYSIS; ESTERS; ETHYLENES; KETONES; NAPROXEN; PALLADIUM; PHOSPHINES; STEREOISOMERISM;

EID: 80053492633     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja2066829     Document Type: Article

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