Selective arylation, alkenylation, and cyclization of dibromonaphthols, using visible light, via carbene intermediates

Journal of Organic Chemistry

Volumn 74, Issue 15, 2009, Pages 5311-5319

  Verga, Daniela ^a   Doria, Filippo ^a   Mella, Mariella ^a   Freccero, Mauro ^a  

^a UNIVERSITY OF PAVIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

2-NAPHTHOLS; ALKENYLATION; ARYLATION; CARBENE; CHEMICAL EQUATIONS; CYCLIZATION REACTIONS; DIRADICALS; HYDROBROMIC ACID; LASER FLASH PHOTOLYSIS; NAPHTHOQUINONE; PRODUCT DISTRIBUTIONS; VINYL ETHERS; VISIBLE LIGHT;

ACETONITRILE; CYCLIZATION; ETHERS; INORGANIC ACIDS; KETONES; NITROGEN COMPOUNDS; PHENOLS; PHOTOLYSIS;

MOLECULAR OXYGEN;

1,2 NAPHTHOQUINONE O OXIDE; 4,7 DIBROMO 3 HYDROXY N,N DIMETHYLNAPHTHALENE 2 CARBOXAMIDE; 4,7 DIBROMO-3 HYDROXYNAPHTHALENE 2 CARBOXAMIDE; ACETONITRILE; ACRYLONITRILE; ALLYTRIMETHYLSILANE; ALPHA KETOCARBENE; CARBENE; ELECTROPHILE; ETHER DERIVATIVE; ETHYL VINYL ETHER; HYDROBROMIC ACID; NAPHTHOL DERIVATIVE; OXYGEN; PHOSPHATE; PYRROLE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CYCLIZATION; DRUG STRUCTURE; LIGHT; PH MEASUREMENT; PHOTOLYSIS; SUBSTITUTION REACTION;

EID: 68049088816     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900793b     Document Type: Article

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