Synthesis of 2,9-dialkylated phenanthro[1,2-b:8,7-b′]dithiophenes via cross-coupling reactions and sequential Lewis acid-catalyzed regioselective cycloaromatization of epoxide

Tetrahedron Letters

Volumn 55, Issue 29, 2014, Pages 4002-4005

  Hyodo, Keita ^a   Nonobe, Hikaru ^a   Nishinaga, Shuhei ^a   Nishihara, Yasushi ^a,b  

^a OKAYAMA UNIVERSITY   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Boron; Negishi coupling; Phenacenes; Suzuki Miyaura coupling; Zinc

Indexed keywords

1,4 DIBROMOBENZENE; 2 THIENYLBORON; BROMOBENZENE; EPOXIDE; LEWIS ACID; PHENANTHRO[1,2 B:8,7 B']DITHIOPHENE DERIVATIVE; UNCLASSIFIED DRUG; ZINC DERIVATIVE; BENZENE DERIVATIVE; PALLADIUM; PHENANTHRENE DERIVATIVE; THIOPHENE DERIVATIVE; ZINC;

ALKYLATION; AROMATIZATION; ARTICLE; BROMINATION; CATALYSIS; CATALYST; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; CYCLIZATION; CYCLOAROMATIZATION; EPOXIDATION; SUZUKI REACTION; ELECTROPHILICITY; FILM; REACTION TIME; SOLUBILITY; SYNTHESIS;

EID: 84903275596     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.05.035     Document Type: Article

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