A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones

Journal of the American Chemical Society

Volumn 137, Issue 24, 2015, Pages 7632-7635

  Miles, Dillon H ^a   Guasch, Joan ^a   Toste, F Dean ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

KETONES;

ENANTIOSELECTIVE; ENANTIOSELECTIVE ADDITION; HYDRAZONES; KINETIC RESOLUTION;

ENANTIOSELECTIVITY;

ALKENE DERIVATIVE; ANILINE DERIVATIVE; COPPER DERIVATIVE; HYDRAZONE DERIVATIVE; KETONE DERIVATIVE; NUCLEOPHILE; PHOSPHORIC ACID; ALKENE; AROMATIC HYDROCARBON; KETONE;

AMINATION; ARTICLE; CATALYST; CHIRALITY; DECOMPOSITION; ELECTROPHILICITY; ENANTIOMER; ENANTIOSELECTIVITY; HYDROLYSIS; NUCLEOPHILICITY; PROTON TRANSPORT; REACTION TIME; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ALKENES; AMINATION; ANILINE COMPOUNDS; HYDRAZONES; HYDROCARBONS, AROMATIC; KETONES; STEREOISOMERISM;

EID: 84933055655     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b04518     Document Type: Article

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