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Volumn , Issue 11, 2000, Pages 987-988

Trifluoromethylthiodediazoniation: A simple, efficient route to trifluoromethyl aryl sulfides

Author keywords

[No Author keywords available]

Indexed keywords

DIAZONIUM COMPOUND; ORGANOFLUORINE DERIVATIVE;

EID: 0034616857     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b002560g     Document Type: Article
Times cited : (108)

References (21)
  • 1
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    • ed. R. E. Banks, Ellis Horwood Ltd, Chichester
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    • (1979) Organofluorine Chemical and Their Industrial Applications
    • Filler, R.1
  • 2
    • 0003536898 scopus 로고
    • ed. R. E. Banks, B. E. Smart and C. Tatlow, Plenum Press, New York
    • R. Filler, in Organofluorine Chemical and their Industrial Applications, ed. R. E. Banks, Ellis Horwood Ltd, Chichester, 1979; B. E. Smart, in Organofluorine Chemistry. Principles and Commercial Applications, ed. R. E. Banks, B. E. Smart and C. Tatlow, Plenum Press, New York, 1994; R. M. DeMarinis and W. M. Bryan, J. Org. Chem., 1977, 42, 2024.
    • (1994) Organofluorine Chemistry. Principles and Commercial Applications
    • Smart, B.E.1
  • 3
    • 0017784496 scopus 로고
    • R. Filler, in Organofluorine Chemical and their Industrial Applications, ed. R. E. Banks, Ellis Horwood Ltd, Chichester, 1979; B. E. Smart, in Organofluorine Chemistry. Principles and Commercial Applications, ed. R. E. Banks, B. E. Smart and C. Tatlow, Plenum Press, New York, 1994; R. M. DeMarinis and W. M. Bryan, J. Org. Chem., 1977, 42, 2024.
    • (1977) J. Org. Chem. , vol.42 , pp. 2024
    • DeMarinis, R.M.1    Bryan, W.M.2
  • 4
    • 0026760246 scopus 로고
    • M. A. McClinton and D. A. McClinton, Tetrahedron, 1992, 37, 6555; J. F. Harris, J. Org. Chem., 1967, 32, 2063; J. H. Clark, D. Wails and T. W. Bastock, Aromatic Fluorination, CRC Press, New York, 1997.
    • (1992) Tetrahedron , vol.37 , pp. 6555
    • McClinton, M.A.1    McClinton, D.A.2
  • 5
    • 0001326546 scopus 로고
    • M. A. McClinton and D. A. McClinton, Tetrahedron, 1992, 37, 6555; J. F. Harris, J. Org. Chem., 1967, 32, 2063; J. H. Clark, D. Wails and T. W. Bastock, Aromatic Fluorination, CRC Press, New York, 1997.
    • (1967) J. Org. Chem. , vol.32 , pp. 2063
    • Harris, J.F.1
  • 6
    • 85051828730 scopus 로고    scopus 로고
    • CRC Press, New York
    • M. A. McClinton and D. A. McClinton, Tetrahedron, 1992, 37, 6555; J. F. Harris, J. Org. Chem., 1967, 32, 2063; J. H. Clark, D. Wails and T. W. Bastock, Aromatic Fluorination, CRC Press, New York, 1997.
    • (1997) Aromatic Fluorination
    • Clark, J.H.1    Wails, D.2    Bastock, T.W.3
  • 7
    • 0030590504 scopus 로고    scopus 로고
    • T. Billard and B. R. Langlois, Tetrahedron Lett., 1996, 37, 6865; T. Billard, S. Large and B. R. Langlois, Tetrahedron Lett., 1997, 38, 65.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 6865
    • Billard, T.1    Langlois, B.R.2
  • 12
    • 0001590919 scopus 로고
    • Diazonium salts were prepared via the method described in A. Roe, Org. React., 1949, 5, 193.
    • (1949) Org. React. , vol.5 , pp. 193
    • Roe, A.1
  • 14
    • 0342562294 scopus 로고    scopus 로고
    • note
    • 2), 1103s (C-F), 777m (C-S).
  • 21
    • 0343432147 scopus 로고    scopus 로고
    • note
    • 3), followed by tert-butyl nitrite in acetonitrile. Evolution of a gas was observed and a darkening in the colour of the reaction mixture. Samples for GC, GC-MS and NMR analysis were first added to saturated calcium carbonate solution and then extracted with diethyl ether.


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