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Volumn , Issue 23, 2005, Pages 5089-5093

Chemoselective lithiation of 1-Bromo-n-chloroalkanes

Author keywords

Chlorohydrins; Diols; Electrophilic substitution 1 Bromo n chloroalkanes; Selective lithiation

Indexed keywords


EID: 28444459256     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200500407     Document Type: Article
Times cited : (8)

References (49)
  • 3
    • 0002148313 scopus 로고
    • (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson, A. McKillop), Pergamon, Oxford
    • c) M. Gray, M. Tinkel, V. Snieckus, Comprehensive Organometallic Chemistry II (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson, A. McKillop), Pergamon, Oxford, 1995, vol. 11, pp. 1-92;
    • (1995) Comprehensive Organometallic Chemistry II , vol.11 , pp. 1-92
    • Gray, M.1    Tinkel, M.2    Snieckus, V.3
  • 14
    • 23944484430 scopus 로고    scopus 로고
    • g) See also the special issue of Tetrahedron Symposium in Print dedicated to 'Functionalized Organolithium Compounds' (Guest editors: C. Najera, M. Yus, Tetrahedron 2005, 61, 3125-3450).
    • (2005) Tetrahedron , vol.61 , pp. 3125-3450
    • Najera, C.1    Yus, M.2
  • 15
    • 0034681431 scopus 로고    scopus 로고
    • The carbon-fluorine bond is much more difficult to lithiate. See, for instance: a) D. Guijarro, M. Yus, Tetrahedron 2000, 56, 1135-1138;
    • (2000) Tetrahedron , vol.56 , pp. 1135-1138
    • Guijarro, D.1    Yus, M.2
  • 26
    • 0030496093 scopus 로고    scopus 로고
    • For reviews, see: a) M. Yus, Chem. Soc. Rev. 1996, 25, 155-161;
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 155-161
    • Yus, M.1
  • 28
    • 0034904455 scopus 로고    scopus 로고
    • c) M. Yus, Synlett 2001, 1197-1205;
    • (2001) Synlett , pp. 1197-1205
    • Yus, M.1
  • 31
    • 28444486246 scopus 로고    scopus 로고
    • [1f], chapter 11
    • [1f], chapter 11.
  • 32
    • 0036860845 scopus 로고    scopus 로고
    • For a review on metal-promoted dehalogenation reactions, see: F. Alonso, I. P. Beletskaya, M. Yus, Chem. Rev. 2002, 102, 4009-4091.
    • (2002) Chem. Rev. , vol.102 , pp. 4009-4091
    • Alonso, F.1    Beletskaya, I.P.2    Yus, M.3
  • 33
    • 0000148742 scopus 로고
    • For an example of application of this methodology for the generation of functionalized organolithium compounds by chlorine-lithium exchange, see: D. J. Ramón, M. Yus, J. Org. Chem. 1991, 56, 3825-3831.
    • (1991) J. Org. Chem. , vol.56 , pp. 3825-3831
    • Ramón, D.J.1    Yus, M.2
  • 35
    • 2542447275 scopus 로고    scopus 로고
    • Erratum: M. Yus, B. Moreno, F. Foubelo, Synthesis 2004, 1720
    • We have seen in other cases that on performing the arene-promoted reactions at higher scales a considerable increment of the yield is generally obtained. See, for instance: M. Yus, B. Moreno, F. Foubelo, Synthesis 2004, 1115-1118; Erratum: M. Yus, B. Moreno, F. Foubelo, Synthesis 2004, 1720.
    • (2004) Synthesis , pp. 1115-1118
    • Yus, M.1    Moreno, B.2    Foubelo, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.