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Volumn 53, Issue 12, 2012, Pages 1493-1496

First synthesis of 1-(indol-2-yl)azulenes by the Vilsmeier-Haack type arylation with triflic anhydride as an activating reagent

Author keywords

Azulene; Coupling reaction; Electrophilic substitution; Indole

Indexed keywords

ACID ANHYDRIDE; AZULENE DERIVATIVE; DIHYDROPYRIDINE DERIVATIVE; ELECTROPHILE; INDOLE DERIVATIVE; REAGENT; TRIFLUOROMETHANESULFONIC ACID;

EID: 84857235547     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.01.044     Document Type: Article
Times cited : (30)

References (32)
  • 26
    • 0141459242 scopus 로고    scopus 로고
    • The C-N bond formation between 2-bromoazulene and indole under the palladium-catalyzed Hartwig-Buchwald's condition was reported by our group
    • The C-N bond formation between 2-bromoazulene and indole under the palladium-catalyzed Hartwig-Buchwald's condition was reported by our group R. Yokoyama, S. Ito, T. Okujima, T. Kubo, M. Yasunami, A. Tajiri, and N. Morita Tetrahedron 59 2003 8191 8198
    • (2003) Tetrahedron , vol.59 , pp. 8191-8198
    • Yokoyama, R.1    Ito, S.2    Okujima, T.3    Kubo, T.4    Yasunami, M.5    Tajiri, A.6    Morita, N.7
  • 29
    • 0000840987 scopus 로고
    • The ester function of 2-arylazulenes at the 1-position exhibit decarboxylation under the acidic conditions
    • The ester function of 2-arylazulenes at the 1-position exhibit decarboxylation under the acidic conditions T. Morita, and K. Takase Bull. Chem. Soc. Jpn. 55 1982 1144 1152
    • (1982) Bull. Chem. Soc. Jpn. , vol.55 , pp. 1144-1152
    • Morita, T.1    Takase, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.