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Volumn , Issue 11, 2008, Pages 1707-1716

N-arylations of nitrogen-containing heterocycles with aryl and heteroaryl halides using a copper(I) oxide nanoparticle/1,10-phenanthroline catalytic system

Author keywords

1,10 phenanthroline; Copper(I) oxide nanoparticles; Halides; Heterocycles; N arylations

Indexed keywords

COMPUTER NETWORKS; COPPER; NITROGEN; NONMETALS; SULFUR COMPOUNDS;

EID: 45249121205     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067014     Document Type: Article
Times cited : (50)

References (77)
  • 1
    • 3042795630 scopus 로고    scopus 로고
    • For selected recent examples, see: a
    • For selected recent examples, see: (a) Zhong, C.; He, J.; Xue, C; Li, Y. Bioorg. Med. Chem. 2004, 12, 4009.
    • (2004) Bioorg. Med. Chem , vol.12 , pp. 4009
    • Zhong, C.1    He, J.2    Xue, C.3    Li, Y.4
  • 15
    • 0003995267 scopus 로고    scopus 로고
    • For selected papers on palladium-catalyzed N-arylations of imidazoles, see: a, Negishi, E, Ed, Wiley Interscience: New York
    • For selected papers on palladium-catalyzed N-arylations of imidazoles, see: (a) Hartwig, J. F. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley Interscience: New York, 2002, 1051.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , pp. 1051
    • Hartwig, J.F.1
  • 18
    • 9644277114 scopus 로고    scopus 로고
    • For selected reviews on the use of copper as the catalyst, see: a
    • For selected reviews on the use of copper as the catalyst, see: (a) Beletskaya, I. P.; Cheprakov, A. V. Coord. Chem. Rev. 2004, 248, 2337.
    • (2004) Coord. Chem. Rev , vol.248 , pp. 2337
    • Beletskaya, I.P.1    Cheprakov, A.V.2
  • 20
    • 0345329013 scopus 로고
    • For a paper on N-arylations of imidazoles with aryl halides mediated by stoichiometric copper, see
    • For a paper on N-arylations of imidazoles with aryl halides mediated by stoichiometric copper, see: Lindley, J. Tetrahedron 1984, 40, 1433.
    • (1984) Tetrahedron , vol.40 , pp. 1433
    • Lindley, J.1
  • 47
    • 33751154516 scopus 로고    scopus 로고
    • For selected representative papers on copper-catalyzed N-arylations of imidazoles with other reagents, see: (a) Lopez-Alvarado, P, Avendaño, C, Menéndez, J. C. J. Org. Chem. 1995, 60, 5678
    • For selected representative papers on copper-catalyzed N-arylations of imidazoles with other reagents, see: (a) Lopez-Alvarado, P.; Avendaño, C.; Menéndez, J. C. J. Org. Chem. 1995, 60, 5678.
  • 57
    • 0034682150 scopus 로고    scopus 로고
    • For selected papers on N-arylations of indoles using palladium, see: a
    • For selected papers on N-arylations of indoles using palladium, see: (a) Old, D. W.; Harris, M. C.; Buchwald, S. L. Org. Lett. 2000, 2, 1403.
    • (2000) Org. Lett , vol.2 , pp. 1403
    • Old, D.W.1    Harris, M.C.2    Buchwald, S.L.3
  • 65
    • 5044231354 scopus 로고
    • For a paper on solvent-free, copper-catalyzed amination reactions of aryl halides with amines, see
    • For a paper on solvent-free, copper-catalyzed amination reactions of aryl halides with amines, see: Gajare, A. S.; Toyota, K.; Yoshifuji, M.; Ozawa, F. Chem. Commun. 2004, 1994.
    • (1994) Chem. Commun , vol.2004
    • Gajare, A.S.1    Toyota, K.2    Yoshifuji, M.3    Ozawa, F.4
  • 67
    • 0000586886 scopus 로고    scopus 로고
    • For representative papers on transition-metal-catalyzed cross-coupling reactions promoted by quaternary ammonium compounds, in particular TBAB, see: (a) Badone, D, Baroni, M, Cardamone, R, Ielmini, A, Guzzi, U. J. Org. Chem. 1997, 62, 7170
    • For representative papers on transition-metal-catalyzed cross-coupling reactions promoted by quaternary ammonium compounds, in particular TBAB, see: (a) Badone, D.; Baroni, M.; Cardamone, R.; Ielmini, A.; Guzzi, U. J. Org. Chem. 1997, 62, 7170.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.