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0029148001
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(S)-(+)-4,4,4-Trifluoro-3-(indole-3-)butyric acid, a novel fluorinated plant growth regulator
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0013557550
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Studies on the plant growth regulators containing fluorines: Biological activities of 4,4,4-trifluoro-3-(indole-3-)butyric acid (TFIBA) (1)
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in Japanese with English abstract
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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)
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Gautam, R.K.5
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3
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0027422041
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Enzymatic preparation of both enantiomers of 4,4,4-trifluoro-3-(indole-3-)butyric acid, a novel plant growth regulator
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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).
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4
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0029168176
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Preparation and lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(naphthyl)ethanols
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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).
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5
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0029962076
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Optical resolution of 2,2,2-trifluoro-1-(9-phenanthryl) ethanol via enzymatic alcoholysis of its activated ester
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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).
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6
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0029350785
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Fitness of lipases and substrates in lipase-catalyzed resolution
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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)
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Nakamura, K.1
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7
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0029125707
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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
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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).
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9
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0010787139
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Effect of the fluorine atom on stereocontrolled synthesis: Chemical or microbial methods
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Welch, J. T. (ed.), Maple Press, York
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Kitazume, T.1
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0028276953
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The resolution of tertiary α-acetylene-acetate esters by the lipase from Candida cylindracea
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0028860083
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Lipase-catalyzed enantioselective synthesis of naphthyl trifluoromethyl carbinols and their corresponding non-fluorinated counterparts
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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).
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0028093428
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Lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(indole-3-) ethanols in organic solvents
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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).
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85007989542
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Lipase-catalyzed optical resolution of 2,2,2-trifluoro-1-(1-naphthyl)ethanol
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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).
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0028947418
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A facile preparation of enantiomers of ethyl 4,4,4-trifluoro-3-(indole-3-)butyrate, a novel plant growth regulator
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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).
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20644469267
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Enzymes in asymmetric synthesis: Effect of reaction media on the PLE catalyzed hydrolysis of diesters
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Oxalate as an activated ester group in lipase-catalyzed enantioselective hydrolysis: A versatile approach to δ-α-tocopherol
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