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Volumn 72, Issue 24, 2007, Pages 9329-9334

Facile access to polysubstituted indoles via a cascade Cu-catalyzed arylation - Condensation process

Author keywords

[No Author keywords available]

Indexed keywords

2-HALOTRIFLUOROACETANILIDES; ARYLATION; FACILE ACCESS;

EID: 36649030328     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702059q     Document Type: Article
Times cited : (125)

References (45)
  • 5
    • 33749832654 scopus 로고    scopus 로고
    • (b) Kuethe, J. T. Chimia 2006, 60, 543.
    • (2006) Chimia , vol.60 , pp. 543
    • Kuethe, J.T.1
  • 27
    • 0038223924 scopus 로고    scopus 로고
    • For selected examples, see: a
    • For selected examples, see: (a) Gathergood, N.; Scammells, P. J. Org. Lett. 2003, 5, 921.
    • (2003) Org. Lett , vol.5 , pp. 921
    • Gathergood, N.1    Scammells, P.J.2
  • 35
    • 0037165422 scopus 로고    scopus 로고
    • For recent studies on the CuI-catalyzed coupling between aryl halides and activated methylene compounds, see: (a) Hennessy, E. J, Buchwald, S. L. Org. Lett. 2002, 4, 269
    • For recent studies on the CuI-catalyzed coupling between aryl halides and activated methylene compounds, see: (a) Hennessy, E. J.; Buchwald, S. L. Org. Lett. 2002, 4, 269.
  • 45
    • 34548062130 scopus 로고    scopus 로고
    • During the submission of this manuscript, Tanimori and co-workers disclosed their studies on the synthesis of indoles via binol-promoted Cul-catalyzed coupling of 2-iodoaniline with β-keto esters, but no substituted 2-iodoanilines were explored. See: Tanimori, S.; Ura, H.; Kirhata, M. Eur. J. Org. Chem. 2007, 3977.
    • During the submission of this manuscript, Tanimori and co-workers disclosed their studies on the synthesis of indoles via binol-promoted Cul-catalyzed coupling of 2-iodoaniline with β-keto esters, but no substituted 2-iodoanilines were explored. See: Tanimori, S.; Ura, H.; Kirhata, M. Eur. J. Org. Chem. 2007, 3977.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.