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Volumn , Issue 15, 2006, Pages 2375-2378

Synthesis of oxygenated carbazoles by palladium-mediated oxidative double C-H activation of diarylamines assisted by microwave irradiation

Author keywords

C H activation; Carbazoles; Cyclizations; Microwave assisted synthesis; Transition metals

Indexed keywords

3 METHOXYDIPHENYLAMINE; ACETIC ACID; ALKALOID DERIVATIVE; AMINE; CARBAZOLE DERIVATIVE; CARBAZOMYCIN A; CARBAZOMYCIN B; DIPHENYLAMINE; FLUORESCENT DYE; GLYCOZOLIDINE; MURRAYAFOLINE A; MURRAYAQUINONE A; N,N DIMETHYLFORMAMIDE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 33749347309     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-950415     Document Type: Article
Times cited : (36)

References (58)
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    • note
    • General procedure: The suitable diarylamine 1 (1 equiv) and palladium acetate (2 equiv) were thoroughly mixed. After addition of three drops of DMF, the mixture was irradiated in a domestic microwave oven at 600 W for l min or 1.5 min, as specified in Table 2. After completion of the reaction, carbazoles 2 were purified through silica gel via flash column chromatography, eluting with a PE-EtOAc (8:2) mixture.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.