Palladium-catalyzed α-arylation of zinc enolates of esters: Reaction conditions and substrate scope

Journal of Organic Chemistry

Volumn 78, Issue 17, 2013, Pages 8250-8266

  Hama, Takuo ^a   Ge, Shaozhong ^b,c   Hartwig, John F ^a,b,c  

^a YALE UNIVERSITY   (United States)

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

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO FUNCTIONALITY; ARYL BROMIDES; BROMOARENES; METAL ENOLATES; PALLADIUM-CATALYZED; REACTION CONDITIONS; REFORMATSKY REAGENTS; ROOM TEMPERATURE;

ALKALI METALS; AROMATIC COMPOUNDS; CATALYSIS; CHLORINE COMPOUNDS; ESTERIFICATION; OLEFINS; PALLADIUM COMPOUNDS; ZINC;

ESTERS;

ACETIC ACID DERIVATIVE; ALKALI METAL; ALPHA ALKOXYESTER; BROMIDE; BROMINE DERIVATIVE; BROMOARENE; BROMOPYRIMIDINE; ESTER; FUNCTIONAL GROUP; ISOBUTYRIC ACID DERIVATIVE; LACTONE; PALLADIUM; PENTAPHENYLFERROCENYL DI TERT BUTYLPHOSPHINE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PROPIONIC ACID DERIVATIVE; PYRIMIDINE DERIVATIVE; REAGENT; TOLUENE; UNCLASSIFIED DRUG; ZINC; ZINC CHLORIDE; ZINC ENOLATE;

ARTICLE; ARYLATION; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; REFORMATSKY REACTION; ROOM TEMPERATURE;

CATALYSIS; ESTERS; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; PALLADIUM; ZINC;

EID: 84883825239     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo401476f     Document Type: Article

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