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Volumn 746, Issue , 1999, Pages 22-37

Asymmetric syntheses of fluoroorganic compounds via chiral organoboranes

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EID: 0042912934     PISSN: 00976156     EISSN: None     Source Type: Book Series    
DOI: 10.1021/bk-2000-0746.ch002     Document Type: Article
Times cited : (2)

References (70)
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    • Biomedical frontiers of fluorine chemistry
    • American Chemical Society, Washington DC
    • For several recent reviews see: Biomedical Frontiers of Fluorine Chemistry, Ojima, I.; McCarthy, J. R.; Welch, J. T. Eds. ACS Symposium Series 639, American Chemical Society, Washington DC, 1996.
    • (1996) ACS Symposium Series , vol.639
    • Ojima, I.1    McCarthy, J.R.2    Welch, J.T.3
  • 7
    • 0004236901 scopus 로고    scopus 로고
    • Reductions in organic chemistry
    • American Chemical Society, Washington, DC
    • Reductions in Organic Chemistry. American Chemical Society Symposium Series # 641. Abdel-Magid, A. F. Ed., American Chemical Society, Washington, DC, 1996.
    • (1996) American Chemical Society Symposium Series , vol.641
    • Abdel-Magid, A.F.1
  • 13
    • 0010176851 scopus 로고
    • DIP-Chloride™ is the Trade Mark of the Aldrich Chemical Company
    • (a) Brown, H. C.; Chandrasekharan, J.; Ramachandran, P. V. J. Am. Chem. Soc. 1988, 110, 1539. DIP-Chloride™ is the Trade Mark of the Aldrich Chemical Company.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 1539
    • Brown, H.C.1    Chandrasekharan, J.2    Ramachandran, P.V.3
  • 16
    • 84981828672 scopus 로고
    • The S-configuration of the fluoro alcohol has opposite stereochemistry compared to the S-isomer of α-phenethanol. This is an artifact of Cahn-Ingold-Prelog priority rules. Cahn, R. S.; Ingold, C.; Prelog, V. Angew. Chem. Int. Ed. Engl. 1966, 5, 385.
    • (1966) Angew. Chem. Int. Ed. Engl. , vol.5 , pp. 385
    • Cahn, R.S.1    Ingold, C.2    Prelog, V.3
  • 18
    • 0003978131 scopus 로고
    • Prentice Hall: Englewood Cliffs, N.J.
    • For an early extensive discussion of this topic, see: Morrison, J. D.; Mosher, H. S. Asymmetric Organic Reactions, Prentice Hall: Englewood Cliffs, N.J., 1971, pp 160-218.
    • (1971) Asymmetric Organic Reactions , pp. 160-218
    • Morrison, J.D.1    Mosher, H.S.2
  • 37
    • 0041731400 scopus 로고    scopus 로고
    • In ref. 1 Chapter 9
    • Kirk, K. L. In ref. 1 Chapter 9.
    • Kirk, K.L.1
  • 51
    • 0041731399 scopus 로고    scopus 로고
    • in ref. 2, Chapter 2
    • For reviews on the aldol reactions, see: (a) Heathcock, C. H. in ref. 2, Vol.3, Chapter 2.
    • , vol.3
    • Heathcock, C.H.1
  • 58
    • 0025906950 scopus 로고
    • For the asymmetric aldol reactions of enolborinates using different chiral auxiliaries, see: (a) Corey, E. J.; Choi, S. Tetrahedron Lett. 1991, 32, 2857.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2857
    • Corey, E.J.1    Choi, S.2


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