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Volumn 52, Issue 27, 2013, Pages 6953-6957

Silver-catalyzed isocyanide-alkyne cycloaddition: A general and practical method to oligosubstituted pyrroles

Author keywords

alkynes; cycloaddition; isocyanides; oligosubstituted pyrroles; silver carbonate

Indexed keywords

ALKYNES; INTERNAL ALKYNES; ISOCYANIDES; LIGAND-FREE; OLIGOSUBSTITUTED PYRROLES; PRACTICAL METHOD; SILVER CARBONATE; TERMINAL ALKYNE;

EID: 84879353936     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201302024     Document Type: Article
Times cited : (278)

References (59)
  • 19
    • 70350038072 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 8318-8320
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 8318-8320
  • 25
    • 84875696858 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 4012-4015.
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 4012-4015
  • 27
    • 84891029339 scopus 로고    scopus 로고
    • (Eds.: F. Diederich, P. J. Stang, R. R. Tykwinski), Wiley-VCH, Weinheim.
    • Acetylene Chemistry (Eds.:, F. Diederich, P. J. Stang, R. R. Tykwinski,), Wiley-VCH, Weinheim, 2005.
    • (2005) Acetylene Chemistry
  • 31
    • 24944474895 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5664-5667
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5664-5667
  • 34
    • 58449122468 scopus 로고    scopus 로고
    • Only one report involving the tedious in situ preparation of copper acetylides is known to date, see.
    • Only one report involving the tedious in situ preparation of copper acetylides is known to date, see:, A. V. Lygin, O. V. Larionov, V. S. Korotkov, A. de Meijere, Chem. Eur. J. 2009, 15, 227-236.
    • (2009) Chem. Eur. J. , vol.15 , pp. 227-236
    • Lygin, A.V.1    Larionov, O.V.2    Korotkov, V.S.3    De Meijere, A.4
  • 38
    • 84891567388 scopus 로고    scopus 로고
    • (Eds.: M, Harmata), Wiley, Hoboken.
    • Silver in Organic Chemistry (Eds.:, M, Harmata,), Wiley, Hoboken, 2010.
    • (2010) Silver in Organic Chemistry
  • 45
    • 79960625611 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 7140-7143
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7140-7143
  • 56
    • 79952634665 scopus 로고    scopus 로고
    • For a review on carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations, see:, L. Ackermann, Chem. Rev. 2011, 111, 1315-1345.
    • (2011) Chem. Rev. , vol.111 , pp. 1315-1345
    • Ackermann, L.1
  • 59
    • 84879364315 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 6958-6961
    • This Communication is published back-to-back with the following study: M. Gao, C. He, H. Chen, R. Bai, B. Cheng, A. Lei, Angew. Chem. 7096-7099; Angew. Chem. Int. Ed. 6958-6961.
    • Angew. Chem. , pp. 7096-7099
    • Gao, M.1    He, C.2    Chen, H.3    Bai, R.4    Cheng, B.5    Lei, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.