Electrosynthesis of symmetric and highly conjugated benzofuran via a unique ECECCC electrochemical mechanism: Evidence for predominance of electrochemical oxidation versus intramolecular cyclization

Journal of Organic Chemistry

Volumn 72, Issue 10, 2007, Pages 3646-3651

  Nematollahi, Davood ^a   Amani, Amene ^a   Tammari, Esmail ^b  

^a BU ALI SINA UNIVERSITY   (Iran)

^b PAYAME NOOR UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

CONJUGATED BENZOFURAN; ELECTROSYNTHESIS; INTRAMOLECULAR CYCLIZATION; MONOSUBSTITUTED DERIVATIVES;

COULOMETERS; CYCLIZATION; DERIVATIVES; ELECTROCHEMICAL OXIDATION; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

FURAN RESINS;

3 HYDROXY 1H PHENALEN 1 ONE; ACETONITRILE; BENZOFURAN DERIVATIVE; CATECHOL; HYDROQUINONE; PHENALENE DERIVATIVE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; COULOMETRY; CYCLIC POTENTIOMETRY; CYCLIZATION; ELECTROCHEMISTRY; ELECTRODE; MICHAEL ADDITION; OXIDATION; SYNTHESIS;

BENZOFURANS; CYCLIZATION; ELECTROCHEMISTRY; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 34248569317     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062468b     Document Type: Article

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