메뉴 건너뛰기




Volumn 356, Issue 9, 2014, Pages 2051-2060

Practical methods for the synthesis of trifluoromethylated alkynes: Oxidative trifluoromethylation of copper acetylides and alkynes

Author keywords

copper; copper acetylides; oxidative cross coupling; trifluoromethylated alkynes; trifluoromethylation

Indexed keywords


EID: 84902437086     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201400057     Document Type: Article
Times cited : (51)

References (91)
  • 16
    • 84862069135 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 5048-5050
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5048-5050
  • 21
    • 84882268052 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 8214-8264
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 8214-8264
  • 46
    • 84877270612 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 5355-5359.
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 5355-5359
  • 63
    • 84885615410 scopus 로고    scopus 로고
    • For a DFT study of the reaction mechanism, see.
    • For a DFT study of the reaction mechanism, see:, J. Jover, F. Maseras, Chem. Commun. 2013, 49, 10486-10488.
    • (2013) Chem. Commun. , vol.49 , pp. 10486-10488
    • Jover, J.1    Maseras, F.2
  • 68
    • 84860213975 scopus 로고    scopus 로고
    • For the use of other sulfonium-based reagents, see
    • D.-F. Luo, J. Xu, Y. Fu, Q.-X. Guo, Tetrahedron Lett. 2012, 53, 2769-2772. For the use of other sulfonium-based reagents, see
    • (2012) Tetrahedron Lett. , vol.53 , pp. 2769-2772
    • Luo, D.-F.1    Xu, J.2    Fu, Y.3    Guo, Q.-X.4
  • 71
    • 84899832685 scopus 로고    scopus 로고
    • For an additional report on the direct trifluoromethylation of arylacetylenes based on the use of visible-light photoredox catalysis using an iridium catalyst, see
    • For an additional report on the direct trifluoromethylation of arylacetylenes based on the use of visible-light photoredox catalysis using an iridium catalyst, see:, N. Iqbal, J. Jung, S. Park, E. J. Cho, Angew. Chem. 2013, 125, 549-552
    • (2013) Angew. Chem. , vol.125 , pp. 549-552
    • Iqbal, N.1    Jung, J.2    Park, S.3    Cho, E.J.4
  • 72
  • 74
    • 81255162913 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 11062-11087
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 11062-11087
  • 86
    • 79961218918 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 7655-7659
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7655-7659
  • 89
    • 79953675070 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 3793-3798
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 3793-3798


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.