Domino reaction to functionalized 2-hydroxybenzophenones from electron-deficient chromones and 1,3-dicarbonyl compounds

Journal of Organic Chemistry

Volumn 76, Issue 20, 2011, Pages 8495-8500

  Chen, Hong ^a   Xie, Fuchun ^a   Gong, Jian ^a   Hu, Youhong ^a  

^a SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,3-DICARBONYL COMPOUNDS; 2-HYDROXYBENZOPHENONE; CHROMONES; DOMINO PROCESS; DOMINO REACTIONS; ECO-FRIENDLY; ELECTRON-DEFICIENT; FUNCTIONALIZED; INERT ATMOSPHERES; MICHAEL ADDITIONS; ONE POT; TANDEM REACTION SEQUENCES; TRANSITION METAL CATALYSTS;

CATALYSTS; OLEFINS; REACTION KINETICS; SCAFFOLDS; TRANSITION METALS;

KETONES;

1,3 DICARBONYL DERIVATIVE; 2 HYDROXYBENZOPHENONE DERIVATIVE; BENZOPHENONE DERIVATIVE; CARBONYL DERIVATIVE; CHROMONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; CYCLIZATION; DOMINO REACTION; ELIMINATION REACTION; MICHAEL ADDITION; NUCLEOPHILICITY; ONE POT SYNTHESIS; ROOM TEMPERATURE;

BENZOPHENONES; CARBONATES; CATALYSIS; CHEMISTRY, PHARMACEUTICAL; CHROMONES; CYCLIZATION; ELECTRONS; GREEN CHEMISTRY TECHNOLOGY; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 80054102301     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201384f     Document Type: Article

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