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Volumn 69, Issue 9, 1996, Pages 2655-2659

Highly stereocontrolled access to 1,1,1-trifluoro-2,3-epoxypropane via lipase-mediated kinetic resolution of 1,1,1-trifluoro-3-(phenylthio)propan-2-ol and its application

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EID: 0001126919     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.69.2655     Document Type: Article
Times cited : (22)

References (27)
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    • Ref. 2d
    • c) Ref. 2d, see also : K. Furuhashi, M. Shintani, and M. Takagi, Appl. Microbiol. Biotechnol., 23, 218 (1986). (S)-1,1,1-Trifluoro-2,3-epoxypropane (75%ee) is currently available from Japan Energy Co. Enantiomerically enriched 1,1,1-trifluoro-2,3-epoxypropane is also commercially available from Tokyo Kasei Co.
    • (1986) Appl. Microbiol. Biotechnol. , vol.23 , pp. 218
    • Furuhashi, K.1    Shintani, M.2    Takagi, M.3
  • 15
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    • Bakers' yeast reduction of trifluoromethyl ketones, see for example : M. Bacciavelli, A. Forni, I. Movetti, and G. Torre, J. Chem. Soc., Chem. Commun., 1987, 456; G. Guanti, L. Banfi, and E. Narisano, Tetrahedron Lett., 27, 3547 (1986); T. Kitazume and T. Sato, J. Fluorine Chem., 30, 189 (1985); T. Kitazume and N. Ishikawa, Chem. Lett., 1984, 587; T. Kitazume and N. Ishikawa, Chem. Lett., 1983, 237.
    • J. Chem. Soc., Chem. Commun. , vol.1987 , pp. 456
    • Bacciavelli, M.1    Forni, A.2    Movetti, I.3    Torre, G.4
  • 16
    • 0001723127 scopus 로고
    • Bakers' yeast reduction of trifluoromethyl ketones, see for example : M. Bacciavelli, A. Forni, I. Movetti, and G. Torre, J. Chem. Soc., Chem. Commun., 1987, 456; G. Guanti, L. Banfi, and E. Narisano, Tetrahedron Lett., 27, 3547 (1986); T. Kitazume and T. Sato, J. Fluorine Chem., 30, 189 (1985); T. Kitazume and N. Ishikawa, Chem. Lett., 1984, 587; T. Kitazume and N. Ishikawa, Chem. Lett., 1983, 237.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 3547
    • Guanti, G.1    Banfi, L.2    Narisano, E.3
  • 17
    • 0001245659 scopus 로고
    • Bakers' yeast reduction of trifluoromethyl ketones, see for example : M. Bacciavelli, A. Forni, I. Movetti, and G. Torre, J. Chem. Soc., Chem. Commun., 1987, 456; G. Guanti, L. Banfi, and E. Narisano, Tetrahedron Lett., 27, 3547 (1986); T. Kitazume and T. Sato, J. Fluorine Chem., 30, 189 (1985); T. Kitazume and N. Ishikawa, Chem. Lett., 1984, 587; T. Kitazume and N. Ishikawa, Chem. Lett., 1983, 237.
    • (1985) J. Fluorine Chem. , vol.30 , pp. 189
    • Kitazume, T.1    Sato, T.2
  • 18
    • 2842540091 scopus 로고    scopus 로고
    • Bakers' yeast reduction of trifluoromethyl ketones, see for example : M. Bacciavelli, A. Forni, I. Movetti, and G. Torre, J. Chem. Soc., Chem. Commun., 1987, 456; G. Guanti, L. Banfi, and E. Narisano, Tetrahedron Lett., 27, 3547 (1986); T. Kitazume and T. Sato, J. Fluorine Chem., 30, 189 (1985); T. Kitazume and N. Ishikawa, Chem. Lett., 1984, 587; T. Kitazume and N. Ishikawa, Chem. Lett., 1983, 237.
    • Chem. Lett. , vol.1984 , pp. 587
    • Kitazume, T.1    Ishikawa, N.2
  • 19
    • 2842567946 scopus 로고    scopus 로고
    • Bakers' yeast reduction of trifluoromethyl ketones, see for example : M. Bacciavelli, A. Forni, I. Movetti, and G. Torre, J. Chem. Soc., Chem. Commun., 1987, 456; G. Guanti, L. Banfi, and E. Narisano, Tetrahedron Lett., 27, 3547 (1986); T. Kitazume and T. Sato, J. Fluorine Chem., 30, 189 (1985); T. Kitazume and N. Ishikawa, Chem. Lett., 1984, 587; T. Kitazume and N. Ishikawa, Chem. Lett., 1983, 237.
    • Chem. Lett. , vol.1983 , pp. 237
    • Kitazume, T.1    Ishikawa, N.2
  • 20
    • 0027212736 scopus 로고
    • M. Shimizu, K. Fujimori, T. Yokota, and T. Fujisawa, Tetrahedron Asymmetry, 4, 835 (1993). Lipase mediated kinetic resolution of fluorine-containig alcohols, see : T. Kitazume and T. Yamazaki, J. Synth. Org. Chem. Jpn., 49, 721 (1991), and the references cited therein.
    • (1993) Tetrahedron Asymmetry , vol.4 , pp. 835
    • Shimizu, M.1    Fujimori, K.2    Yokota, T.3    Fujisawa, T.4
  • 21
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    • and the references cited therein
    • M. Shimizu, K. Fujimori, T. Yokota, and T. Fujisawa, Tetrahedron Asymmetry, 4, 835 (1993). Lipase mediated kinetic resolution of fluorine-containig alcohols, see : T. Kitazume and T. Yamazaki, J. Synth. Org. Chem. Jpn., 49, 721 (1991), and the references cited therein.
    • (1991) J. Synth. Org. Chem. Jpn. , vol.49 , pp. 721
    • Kitazume, T.1    Yamazaki, T.2
  • 24
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    • note
    • Arylarion of 1,1,1-trifluoro-2,3-epoxypropane has been reported recently, see Ref. 2d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.