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Volumn 47, Issue 10, 2008, Pages 1932-1934

C-H functionalization/C-N bond formation: Copper-catalyzed synthesis of benzimidazoles from amidines

Author keywords

C H functionalization; C N bond formation; Copper; Heterocycles; Homogeneous catalysis

Indexed keywords

CHEMICAL BONDS; CHEMICAL REACTIONS; FORMING; FUNCTIONAL GROUPS; SYNTHESIS (CHEMICAL);

EID: 41949118427     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200705420     Document Type: Article
Times cited : (579)

References (42)
  • 1
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    • For recent reviews of C-H functionalization using transition metals, see: a
    • For recent reviews of C-H functionalization using transition metals, see: a) D. Alberico, M. E. Scott, M. Lautens, Chem. Rev. 2007, 107, 174-238;
    • (2007) Chem. Rev , vol.107 , pp. 174-238
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 8
    • 33746307336 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 2619-2622.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 2619-2622
  • 21
    • 33750522129 scopus 로고    scopus 로고
    • for an approach using a stoichiometric amount of copper, see
    • d) for an approach using a stoichiometric amount of copper, see: T. Uemura, S. Imoto, N. Chatani, Chem. Lett. 2006, 35, 842- 843.
    • (2006) Chem. Lett , vol.35 , pp. 842-843
    • Uemura, T.1    Imoto, S.2    Chatani, N.3
  • 35
    • 53549118257 scopus 로고    scopus 로고
    • A similar observation in yield improvement by increasing the steric bulk was made by Bergman and Ellman et al. in a rhodium-catalyzed C-H functionalization. See reference [3b] for details
    • A similar observation in yield improvement by increasing the steric bulk was made by Bergman and Ellman et al. in a rhodium-catalyzed C-H functionalization. See reference [3b] for details.
  • 36
    • 53549090388 scopus 로고    scopus 로고
    • III intermediates, see: S. V. Ley, A. W. Thomas, Angew. Chem. 2003, 115, 5558-5607;
    • III intermediates, see: S. V. Ley, A. W. Thomas, Angew. Chem. 2003, 115, 5558-5607;
  • 37
    • 0345708168 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 5400-5449.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 5400-5449
  • 38
    • 0036170254 scopus 로고    scopus 로고
    • For a report suggesting a copper metallacycle as intermediate, see
    • For a report suggesting a copper metallacycle as intermediate, see: K. Yamada, T. Kubo, H. Tokuyama, T. Fukuyama, Synlett 2002, 231-234.
    • (2002) Synlett , pp. 231-234
    • Yamada, K.1    Kubo, T.2    Tokuyama, H.3    Fukuyama, T.4
  • 39
    • 0035926089 scopus 로고    scopus 로고
    • Copper nitrenes have been discussed in the aziridination of alkenes, see: a
    • Copper nitrenes have been discussed in the aziridination of alkenes, see: a) K. M. Gillespie, E. J. Crust, R. J. Deeth, P. Scott, Chem. Commun. 2001, 785-786;
    • (2001) Chem. Commun , pp. 785-786
    • Gillespie, K.M.1    Crust, E.J.2    Deeth, R.J.3    Scott, P.4
  • 42
    • 53549118832 scopus 로고    scopus 로고
    • See Supporting Information for data and a more detailed discussion
    • See Supporting Information for data and a more detailed discussion.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.