Transition-metal-free direct arylation: Synthesis of halogenated 2-amino-2′-hydroxy-1,1′-biaryls and mechanism by DFT calculations

Journal of the American Chemical Society

Volumn 135, Issue 19, 2013, Pages 7086-7089

  Gao, Hongyin ^a   Ess, Daniel H ^b   Yousufuddin, Muhammed ^c   Kürti, László ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b Brigham Young University   (United States)

^c UNIVERSITY OF TEXAS AT ARLINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BOND CLEAVAGES; C-C BOND FORMATION; CONVENTIONAL METHODS; DFT CALCULATION; LOW TEMPERATURES; PERISELECTIVITY; REGIO-SELECTIVE; SIGMATROPIC REARRANGEMENTS;

AROMATIC COMPOUNDS; DENSITY FUNCTIONAL THEORY; HALOGENATION;

TRANSITION METALS;

2 AMINO 2' HYDROXY 1,1' BIARYL DERIVATIVE; 2 HALONITROBENZENE; AMINE; BENZENE; N, O BIARYLHYDROXYLAMINE; UNCLASSIFIED DRUG;

AROMATIZATION; ARTICLE; ARYLATION; ATOM; DENSITY FUNCTIONAL THEORY; ENTHALPY; HALOGENATION; MOLECULAR MECHANICS; ONE POT SYNTHESIS; REACTION ANALYSIS;

HALOGENATION; HYDROCARBONS, AROMATIC; MODELS, MOLECULAR; STEREOISOMERISM;

EID: 84877799209     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja400897u     Document Type: Article

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