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Volumn 82, Issue 4, 1996, Pages 355-360

Effective preparation of optically active 4,4,4-trifluoro-3-(indole-3-) butyric acid, a novel plant growth regulator, using lipase from Pseudomonas fluorescens

Author keywords

enantioselective hydrolysis; lipase; Pseudomonas fluorescens

Indexed keywords

TRIACYLGLYCEROL LIPASE;

EID: 0029855612     PISSN: 0922338X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0922-338X(96)89150-1     Document Type: Article
Times cited : (7)

References (18)
  • 1
    • 0029148001 scopus 로고
    • (S)-(+)-4,4,4-Trifluoro-3-(indole-3-)butyric acid, a novel fluorinated plant growth regulator
    • Katayama, K., Kato, K., Kimoto, H., and Fujii, S.: (S)-(+)-4,4,4-Trifluoro-3-(indole-3-)butyric acid, a novel fluorinated plant growth regulator. Experientia, 51, 721-724 (1995).
    • (1995) Experientia , vol.51 , pp. 721-724
    • Katayama, K.1    Kato, K.2    Kimoto, H.3    Fujii, S.4
  • 2
    • 0013557550 scopus 로고
    • Studies on the plant growth regulators containing fluorines: Biological activities of 4,4,4-trifluoro-3-(indole-3-)butyric acid (TFIBA) (1)
    • in Japanese with English abstract
    • Kato, K., Katayama, M., Kimoto, H. M., Fujii, S., Gautam, R. K., and Kamuro, Y.: Studies on the plant growth regulators containing fluorines: biological activities of 4,4,4-trifluoro-3-(indole-3-)butyric acid (TFIBA) (1). Reports Gov. Ind. Res. Inst., Nagoya, 42, 215-223 (1993). (in Japanese with English abstract)
    • (1993) Reports Gov. Ind. Res. Inst., Nagoya , vol.42 , pp. 215-223
    • Kato, K.1    Katayama, M.2    Kimoto, H.M.3    Fujii, S.4    Gautam, R.K.5    Kamuro, Y.6
  • 3
    • 0027422041 scopus 로고
    • Enzymatic preparation of both enantiomers of 4,4,4-trifluoro-3-(indole-3-)butyric acid, a novel plant growth regulator
    • Kato, K., Katayama, M., Gautam, R. K., Fujii, S., and Kimoto, H.: Enzymatic preparation of both enantiomers of 4,4,4-trifluoro-3-(indole-3-)butyric acid, a novel plant growth regulator. J. Ferment. Bioeng., 76, 178-183 (1993).
    • (1993) J. Ferment. Bioeng. , vol.76 , pp. 178-183
    • Kato, K.1    Katayama, M.2    Gautam, R.K.3    Fujii, S.4    Kimoto, H.5
  • 4
    • 0029168176 scopus 로고
    • Preparation and lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(naphthyl)ethanols
    • Kato, K., Katayama, M., Gautam, R. K., Fujii, S., and Kimoto, H.: Preparation and lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(naphthyl)ethanols. Biosci. Biotech. Biochem., 59, 271-276 (1995).
    • (1995) Biosci. Biotech. Biochem. , vol.59 , pp. 271-276
    • Kato, K.1    Katayama, M.2    Gautam, R.K.3    Fujii, S.4    Kimoto, H.5
  • 5
    • 0029962076 scopus 로고    scopus 로고
    • Optical resolution of 2,2,2-trifluoro-1-(9-phenanthryl) ethanol via enzymatic alcoholysis of its activated ester
    • Kato, K., Katayama, M., Fujii, S., Fukaya, H., and Kimoto, H.: Optical resolution of 2,2,2-trifluoro-1-(9-phenanthryl) ethanol via enzymatic alcoholysis of its activated ester. J. Ferment. Bioeng., 81, 206-211 (1996).
    • (1996) J. Ferment. Bioeng. , vol.81 , pp. 206-211
    • Kato, K.1    Katayama, M.2    Fujii, S.3    Fukaya, H.4    Kimoto, H.5
  • 6
    • 0029350785 scopus 로고
    • Fitness of lipases and substrates in lipase-catalyzed resolution
    • in Japanese with English abstract
    • Nakamura, K. and Hirose, Y.: Fitness of lipases and substrates in lipase-catalyzed resolution. Yukigosei Kagaku, 53, 668-677 (1995). (in Japanese with English abstract)
    • (1995) Yukigosei Kagaku , vol.53 , pp. 668-677
    • Nakamura, K.1    Hirose, Y.2
  • 7
    • 0029125707 scopus 로고
    • Lipase-catalyzed enantioselectice acylation of alcohols: A predictive active site model for lipase YS to identify which enantiomer of an alcohol reacts faster in this acylation
    • Naemura, K., Fukuda, R., Murata, M., Konishi, M., Hirose, K., and Tobe, Y.: Lipase-catalyzed enantioselectice acylation of alcohols: a predictive active site model for lipase YS to identify which enantiomer of an alcohol reacts faster in this acylation. Tetrahedron: Asymmetry, 6, 2385-2394 (1995).
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 2385-2394
    • Naemura, K.1    Fukuda, R.2    Murata, M.3    Konishi, M.4    Hirose, K.5    Tobe, Y.6
  • 9
    • 0010787139 scopus 로고
    • Effect of the fluorine atom on stereocontrolled synthesis: Chemical or microbial methods
    • Welch, J. T. (ed.), Maple Press, York
    • Kitazume, T. and Yamazaki, T.: Effect of the fluorine atom on stereocontrolled synthesis: chemical or microbial methods, p. 175-185. In Welch, J. T. (ed.), Selective fluorination in organic and bioorganic chemistry. Maple Press, York (1991).
    • (1991) Selective Fluorination in Organic and Bioorganic Chemistry , pp. 175-185
    • Kitazume, T.1    Yamazaki, T.2
  • 10
    • 0028276953 scopus 로고
    • The resolution of tertiary α-acetylene-acetate esters by the lipase from Candida cylindracea
    • O'Hagan, D. and Zaidi, N.: The resolution of tertiary α-acetylene-acetate esters by the lipase from Candida cylindracea. Tetrahedron: Asymmetry, 5, 1111-1118 (1994).
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 1111-1118
    • O'Hagan, D.1    Zaidi, N.2
  • 11
    • 0028860083 scopus 로고
    • Lipase-catalyzed enantioselective synthesis of naphthyl trifluoromethyl carbinols and their corresponding non-fluorinated counterparts
    • Gaspar, J. and Guerraro, A.: Lipase-catalyzed enantioselective synthesis of naphthyl trifluoromethyl carbinols and their corresponding non-fluorinated counterparts. Tetrahedron: Asymmetry, 6, 231-238 (1995).
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 231-238
    • Gaspar, J.1    Guerraro, A.2
  • 12
    • 0028093428 scopus 로고
    • Lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(indole-3-) ethanols in organic solvents
    • Kato, K., Katayama, M., Gautam, R. K., Fujii, S., and Kimoto, H.: Lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(indole-3-) ethanols in organic solvents. J. Ferment. Bioeng., 78, 64-69 (1994).
    • (1994) J. Ferment. Bioeng. , vol.78 , pp. 64-69
    • Kato, K.1    Katayama, M.2    Gautam, R.K.3    Fujii, S.4    Kimoto, H.5
  • 13
    • 85007989542 scopus 로고
    • Lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(1-naphthyl)ethanol
    • Kato, K., Katayama, M., Gautam, R. K., Fujii, S., and Kimoto, H.: Lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(1-naphthyl)ethanol. Biosci. Biotech. Biochem., 58, 1353-1354 (1994).
    • (1994) Biosci. Biotech. Biochem. , vol.58 , pp. 1353-1354
    • Kato, K.1    Katayama, M.2    Gautam, R.K.3    Fujii, S.4    Kimoto, H.5
  • 14
    • 0028947418 scopus 로고
    • A facile preparation of enantiomers of ethyl 4,4,4-trifluoro-3-(indole-3-)butyrate, a novel plant growth regulator
    • Kato, K., Katayama, M., Gautam, R. K., Fujii, S., Fukaya, H., and Kimoto, H.: A facile preparation of enantiomers of ethyl 4,4,4-trifluoro-3-(indole-3-)butyrate, a novel plant growth regulator. J. Ferment. Bioeng., 79, 171-173 (1995).
    • (1995) J. Ferment. Bioeng. , vol.79 , pp. 171-173
    • Kato, K.1    Katayama, M.2    Gautam, R.K.3    Fujii, S.4    Fukaya, H.5    Kimoto, H.6
  • 15
    • 20644469267 scopus 로고
    • Quantitative analyses of biochemical kinetic resolutions of enantiomers
    • Chen, C. S., Fujimoto, Y., Girdaukas, G., and Sih, C. J.: Quantitative analyses of biochemical kinetic resolutions of enantiomers. J. Am. Chem. Soc., 104, 7294-7299 (1982).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 7294-7299
    • Chen, C.S.1    Fujimoto, Y.2    Girdaukas, G.3    Sih, C.J.4
  • 16
    • 0000297996 scopus 로고
    • Enzymes in asymmetric synthesis: Effect of reaction media on the PLE catalyzed hydrolysis of diesters
    • Guanti, G., Banfi, L., Narisano, E., Riva, R., and Thea, S.: Enzymes in asymmetric synthesis: effect of reaction media on the PLE catalyzed hydrolysis of diesters. Tetrahedron Lett., 27, 4639-4642 (1986).
    • (1986) Tetrahedron Lett. , vol.27 , pp. 4639-4642
    • Guanti, G.1    Banfi, L.2    Narisano, E.3    Riva, R.4    Thea, S.5
  • 17
    • 0027379604 scopus 로고
    • Oxalate as an activated ester group in lipase-catalyzed enantioselective hydrolysis: A versatile approach to δ-α-tocopherol
    • Mizuguchi, E. and Achiwa, K.: Oxalate as an activated ester group in lipase-catalyzed enantioselective hydrolysis: a versatile approach to δ-α-tocopherol. Tetrahedron: Asymmetry, 4, 2303-2306 (1993).
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 2303-2306
    • Mizuguchi, E.1    Achiwa, K.2
  • 18
    • 37049087848 scopus 로고
    • Enzymatic resolution of oxalate esters of a tertiary alcohol using porcine pancreatic lipase
    • Backenridge, I., McCague, R., Roberts, S. M., and Turner, N. J.: Enzymatic resolution of oxalate esters of a tertiary alcohol using porcine pancreatic lipase. J. Chem. Soc. Perkin Trans. 1, 1093-1094 (1993).
    • (1993) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 1093-1094
    • Backenridge, I.1    McCague, R.2    Roberts, S.M.3    Turner, N.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.