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Volumn 353, Issue 14-15, 2011, Pages 2761-2774

Synthesis of arylated quinolines by chemo- and site-selective suzuki-miyaura reactions of 5,7-dibromo-8-(trifluoromethanesulfonyloxy)quinoline

Author keywords

catalysis; palladium; quinolines; regioselectivity; Suzuki Miyaura reaction

Indexed keywords


EID: 80054772217     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201100165     Document Type: Article
Times cited : (22)

References (79)
  • 2
    • 0003607021 scopus 로고    scopus 로고
    • in:, (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon, New York, p 245
    • M. Balasubramania, J. G. Keay, in: Comprehensive Heterocyclic Chemistry II, (Eds.:, A. R. Katritzky, C. W. Rees, E. F. V. Scriven,), Pergamon, New York, 1996, Vol. 5, p 245
    • (1996) Comprehensive Heterocyclic Chemistry II , pp. 5
    • Balasubramania, M.1    Keay, J.G.2
  • 15
    • 84944067367 scopus 로고
    • in:, (Eds.: A. R. Katritzky, C. W. Rees), Pergamon, New York, p 395.
    • G. Jones, in: Comprehensive Heterocyclic Chemistry, (Eds.:, A. R. Katritzky, C. W. Rees,), Pergamon, New York, 1984, Vol. 2, p 395.
    • (1984) Comprehensive Heterocyclic Chemistry , pp. 2
    • Jones, G.1
  • 56
    • 0001260285 scopus 로고
    • the original assignment of the regioselectivity was corrected later
    • J. Reisch, G. M. K. B. Gunaherath, J. Heterocycl. Chem. 1993, 30, 1057; the original assignment of the regioselectivity was corrected later
    • (1993) J. Heterocycl. Chem. , vol.30 , pp. 1057
    • Reisch, J.1    Gunaherath, G.M.K.B.2
  • 79
    • 33645454183 scopus 로고    scopus 로고
    • 1H NMR chemical shift values of the non-halogenated parent compounds, see.
    • 1H NMR chemical shift values of the non-halogenated parent compounds, see:, S. T. Handy, Y. Zhang, Chem. Commun. 2006, 299.
    • (2006) Chem. Commun. , pp. 299
    • Handy, S.T.1    Zhang, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.