Electrochemically induced ring-opening/friedel-crafts arylation of chalcone epoxides catalyzed by a triarylimidazole redox mediator

Journal of Organic Chemistry

Volumn 80, Issue 2, 2015, Pages 781-789

  Lu, Nan Ning ^a   Zhang, Ni Tao ^a   Zeng, Cheng Chu ^a   Hu, Li Ming ^a   Yoo, Seung Joon ^b   Little, R Daniel ^b  

^a BEIJING UNIVERSITY OF TECHNOLOGY   (China)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CHEMICAL REACTIONS; CYCLIC VOLTAMMETRY; ELECTROLYSIS; REACTION KINETICS;

CATALYTIC AMOUNTS; CHAIN REACTION; CHALCONE EPOXIDE; CONTROLLED POTENTIAL ELECTROLYSIS; HOMOGENEOUS ELECTRON TRANSFER; OVEROXIDATIONS; OXIDATION POTENTIALS; REDOX MEDIATORS;

ANODIC OXIDATION;

CHALCONE DERIVATIVE; CHALCONE EPOXIDE; IMIDAZOLE DERIVATIVE; TRIARYLIMIDAZOLE; UNCLASSIFIED DRUG; EPOXIDE;

ARTICLE; ARYLATION; CATALYST; CYCLIC POTENTIOMETRY; ELECTROCHEMISTRY; ELECTROLYSIS; ELECTRON TRANSPORT; FRIEDEL CRAFTS REACTION; OXIDATION; OXIDATION REDUCTION POTENTIAL; OXIDATION REDUCTION REACTION; RING OPENING; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY;

CATALYSIS; CHALCONES; EPOXY COMPOUNDS; IMIDAZOLES; MOLECULAR STRUCTURE; OXIDATION-REDUCTION;

EID: 84921276462     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo5022184     Document Type: Article

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