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Volumn 12, Issue 3, 2010, Pages 464-467

First application of an efficient and versatile ligand for copper-catalyzed cross-coupling reactions of vinyl halides with N-heterocycles and phenols

Author keywords

[No Author keywords available]

Indexed keywords

2 PYRIDIN 2 YL 1H BENZOIMIDAZOLE; 2-PYRIDIN-2-YL-1H-BENZOIMIDAZOLE; BENZIMIDAZOLE DERIVATIVE; COPPER; CROSS LINKING REAGENT; HALOGENATED HYDROCARBON; HETEROCYCLIC COMPOUND; LIGAND; PHENOL DERIVATIVE; PYRIDINE DERIVATIVE; VINYL DERIVATIVE;

EID: 75749155782     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9026446     Document Type: Article
Times cited : (71)

References (52)
  • 1
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    • (a) Monnier, F.; Taillefer, M. Angew. Chem., Int. Ed. 2009, 48, 6954(Minireview) and references cited therein.
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 6954
    • Monnier, F.1    Taillefer, M.2
  • 2
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    • (Review) and references cited therein
    • (b) Ley, S. V.; Thomas, A. W. Angew. Chem., Int. Ed. 2003, 42, 5400(Review) and references cited therein,
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5400
    • Ley, S.V.1    Thomas, A.W.2
  • 15
    • 0037473510 scopus 로고    scopus 로고
    • For intamolecular Ullmann Coupling, please see also
    • (o) Nordmann, G.; Buchwald, S. L. J. Am. Chem. Soc. 2003, 125, 4978. For intamolecular Ullmann Coupling, please see also:
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4978
    • Nordmann, G.1    Buchwald, S.L.2
  • 17
    • 51049095122 scopus 로고    scopus 로고
    • For a highlight on recent major developments in C-C, C-N, and C-N coupling, please see
    • (q) Evano, G.; Blanchard, N.; Toumi, M. Chem. Rev 2008, 108, 3054. For a highlight on recent major developments in C-C, C-N, and C-N coupling, please see:
    • (2008) Chem. Rev , vol.108 , pp. 3054
    • Evano, G.1    Blanchard, N.2    Toumi, M.3
  • 19
    • 33845985272 scopus 로고    scopus 로고
    • For vinylation of amide, s please see these leading references
    • (s) Chen, Y.G.; Chen, H.-H. Org. Lett. 2006, 8, 5609. For vinylation of amide, s please see these leading references:
    • (2006) Org. Lett. , vol.8 , pp. 5609
    • Chen, Y.G.1    Chen, H.-H.2
  • 35
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    • Reference 2a and references cited therein
    • (a) Reference 2a and references cited therein,
  • 51
    • 75749127916 scopus 로고    scopus 로고
    • Optimization studies of the reaction conditions were accomplished with nitrogen and oxygen nucleophiles in parallel experiments which led to the same results in terms of yields. For reasons of chemical economy, more conditions were screened in the cases of oxygen nucleophiles (see Suppoting Information) and the best results extended to the nitrogen nucleophiles
    • Optimization studies of the reaction conditions were accomplished with nitrogen and oxygen nucleophiles in parallel experiments which led to the same results in terms of yields. For reasons of chemical economy, more conditions were screened in the cases of oxygen nucleophiles (see Suppoting Information) and the best results extended to the nitrogen nucleophiles.


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