메뉴 건너뛰기




Volumn 8 a, Issue , 2008, Pages 193-241

Esterases

Author keywords

Catalyze; Cholesterol; Hydrolytic; Stereoselectivity; Triglycerides

Indexed keywords

CHOLESTEROL; GENETIC ENGINEERING; STEREOSELECTIVITY;

EID: 84952934990     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527620906.ch4     Document Type: Chapter
Times cited : (11)

References (162)
  • 1
    • 0038514501 scopus 로고
    • Chiral synthons by enantioselective hydrolysis of mesodiesters with pig-liver esterase - substrate-stereoselectivity relationships
    • ADACHI, K., KOBAYASHI, S., OHNO, M. (1986), Chiral synthons by enantioselective hydrolysis of mesodiesters with pig-liver esterase - substrate-stereoselectivity relationships, Chimia 40, 311-314.
    • (1986) , vol.40 , pp. 311-314
    • Adachi, K.1    Kobayashi, S.2    Ohno, M.3
  • 2
    • 0024798016 scopus 로고
    • Enzymatic resolution of methyl 2-alkyl-2-arylacetates
    • AHMAR, M., GIRARD, C., BLOCH, R. (1989), Enzymatic resolution of methyl 2-alkyl-2-arylacetates, Tetrahedron Lett. 30, 7053-7056.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 7053-7056
    • Ahmar, M.1    Girard, C.2    Bloch, R.3
  • 3
    • 37049084053 scopus 로고
    • Enzymatic resolution of a chiral organometallic ester - enantioselective hydrolysis of 2-ethoxycarbonylbuta-1,3-dienetricarbonyl iron by pig-liver esterase
    • ALCOCK, N.W., CROUT, D.H.G., HENDERSON, C.M., THOMAS, S.E. (1988), Enzymatic resolution of a chiral organometallic ester - enantioselective hydrolysis of 2-ethoxycarbonylbuta-1,3-dienetricarbonyl iron by pig-liver esterase, J. Chem. Soc., Chem. Commun., 746-747.
    • (1988) J. Chem. Soc., Chem. Commun. , pp. 746-747
    • Alcock, N.W.1    Crout, D.H.G.2    Henderson, C.M.3    Thomas, S.E.4
  • 4
    • 0000250310 scopus 로고
    • Resolution of a-methyl amino esters by chymotrypsin
    • ANANTHARAMAIAH, G.M., ROSESKE, R.W. (1982) Resolution of a-methyl amino esters by chymotrypsin, Tetrahedron Lett. 23, 3335-3336.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 3335-3336
    • Anantharamaiah, G.M.1    Roseske, R.W.2
  • 5
    • 0020775374 scopus 로고
    • Enantioselective synthesis of the carbocyclic nucleosides ( - )-aristeromycin and ( - )- neplanocin-A by a chemicoenzymatic approach
    • ARITA, M., ADACHI, K., ITO, Y., SAWAI, H., OHNO, M. (1983), Enantioselective synthesis of the carbocyclic nucleosides ( - )-aristeromycin and ( - )- neplanocin-A by a chemicoenzymatic approach, J. Am. Chem. Soc., 105, 4049-4055.
    • (1983) J. Am. Chem. Soc., 105 , vol.105 , pp. 4049-4055
    • Arita, M.1    Adachi, K.2    Ito, Y.3    Sawai, H.4    Ohno, M.5
  • 6
    • 84952882172 scopus 로고
    • Lipase-catalyzed stereoselective hydrolysis of thiolester
    • BABA, N., MIMURA, M., ODA, J., IWASA, J. (1991), Lipase-catalyzed stereoselective hydrolysis of thiolester, Chem. Abstr. 114, 184892u.
    • (1991) Chem. Abstr. , vol.114 , pp. 184892u
    • Baba, N.1    Mimura, M.2    Oda, J.3    Iwasa, J.4
  • 7
    • 0023729050 scopus 로고
    • Phenylacetyl oxymethylene, a carboxyl protecting group removable with immobilized penicillin acylase, useful in benzyl penicillin chemistry
    • BALDARO, E., FAIARDI, D., FUGANTI, C., GRASELLI, P., LAZZARINI, A. (1988), Phenylacetyl oxymethylene, a carboxyl protecting group removable with immobilized penicillin acylase, useful in benzyl penicillin chemistry, Tetrahedron Lett. 29, 4623-4624.
    • (1988) Tetrahedron Lett , vol.29 , pp. 4623-4624
    • Baldaro, E.1    Faiardi, D.2    Fuganti, C.3    Graselli, P.4    Lazzarini, A.5
  • 9
    • 0027300195 scopus 로고
    • Facile access to 2'- 0-acyl prodrugs of 1-(β-D-arabinofuranosyl)- 5(E)-(2-bromovinyl)uracil (BVARAU) via regioselective esterase-catalyzed hydrolysis of 2',3',5 '-triester
    • BARALDI, P.G., BAZZANINI, R., MANFREDINI, S., SIMONI, D., ROBINS, M.J. (1993), Facile access to 2'- 0-acyl prodrugs of 1-(β-D-arabinofuranosyl)- 5(E)-(2-bromovinyl)uracil (BVARAU) via regioselective esterase-catalyzed hydrolysis of 2',3',5 '-triester, Tetruhedron Lett. 34, 3177-3180.
    • (1993) Tetruhedron Lett. , vol.34 , pp. 3177-3180
    • Baraldi, P.G.1    Bazzanini, R.2    Manfredini, S.3    Simoni, D.4    Robins, M.J.5
  • 10
    • 0026746608 scopus 로고
    • The resolution of racemic 1,2-diols by the esterase-catalyzed hydrolysis of the corresponding cyclic carbonate
    • BARTON, P., PAGE, M.I., (1992), The resolution of racemic 1,2-diols by the esterase-catalyzed hydrolysis of the corresponding cyclic carbonate, Tetrahedron 48, 7731-7734.
    • (1992) Tetrahedron , vol.48 , pp. 7731-7734
    • Barton, P.1    Page, M.I.2
  • 11
    • 0027317549 scopus 로고
    • Synthesis of 3-α-alkoxy-4-β-substituted-2-azetidinones from L-(+)-tartaric acid
    • BARTON, D.H.R., CLÉOPHAX, J., GATEAU-OLESKER, A., GÉ, S.D., TACHDJIAN, C. (1993), Synthesis of 3-α-alkoxy-4-β-substituted-2-azetidinones from L-(+)-tartaric acid, Tetrahedron 49, 8381- 8396.
    • (1993) Tetrahedron , vol.49 , pp. 8381-8396
    • Barton, D.H.R.1    CléOphax, J.2    Gateau-Olesker, A.3    Gé, S.D.4    Tachdjian, C.5
  • 12
    • 0027225452 scopus 로고
    • Selectivity in enzyme-catalyzed reactions - preferential hydrolysis of a phenolic acetate in the presence of an aromatic methyl ester by pig-liver esterase
    • BASAK, A., BHATTACHARYA, G., NAG, A. (1993), Selectivity in enzyme-catalyzed reactions - preferential hydrolysis of a phenolic acetate in the presence of an aromatic methyl ester by pig-liver esterase, Biotechnol. Lett. 15, 469-470.
    • (1993) Biotechnol. Lett. , vol.15 , pp. 469-470
    • Basak, A.1    Bhattacharya, G.2    Nag, A.3
  • 13
    • 0028289233 scopus 로고
    • Enzymatic resolution of trans-2-arylcyclohexan-1-ols using crude chicken liver esterase (CCLE) as biocatalyst
    • BASAVAIAH, D., DHARMA RAO, P. (1994), Enzymatic resolution of trans-2-arylcyclohexan-1-ols using crude chicken liver esterase (CCLE) as biocatalyst, Tetrahedron: Asymmetry 5, 223-234.
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 223-234
    • Basavaiah, D.1    Dharma Rao, P.2
  • 14
    • 0028899412 scopus 로고
    • Synthesis of enantiomerically enriched anti-homoallyl alcohals mediated by crude chicken liver esterase (CCLE)
    • BASAVAIAH, D., DHARMA RAO, P. (1995), Synthesis of enantiomerically enriched anti-homoallyl alcohals mediated by crude chicken liver esterase (CCLE), Tetrahedron: Asymmetry 6,789-800.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 789-800
    • Basavaiah, D.1    Dharma Rao, P.2
  • 15
    • 0015918187 scopus 로고
    • A new method for the synthesis of optically active α-amino acids and their N-α-derivatives via acylamino malonates
    • BERGER, A., SMOLARSKY, M., KURN, N., BOSSHARD, H.R. (1973), A new method for the synthesis of optically active α-amino acids and their N-α-derivatives via acylamino malonates, J. Org. Chem. 38, 457.
    • (1973) J. Org. Chem. , vol.38 , pp. 457
    • Berger, A.1    Smolarsky, M.2    Kurn, N.3    Bosshard, H.R.4
  • 16
    • 0000566588 scopus 로고
    • Lipase-catalyzed stereoselective thiotransesterification of mercapto esters
    • BIANCHI, D., CESTI, P. (1990), Lipase-catalyzed stereoselective thiotransesterification of mercapto esters, J. Org. Chem. 55, 5657-5659.
    • (1990) J. Org. Chem. , vol.55 , pp. 5657-5659
    • Bianchi, D.1    Cesti, P.2
  • 17
    • 0041131871 scopus 로고
    • Enzyme catalyzed- hydrolysis of dialkylated propanedioic acid diesters, chain-length dependent reversal of enantioselectivity
    • BJÖRKLING, F., BOUTELJE, J., GATENBECK, S., HULT, K., NORIN, T., SZMULIK, P. ( 1985a), Enzyme catalyzed- hydrolysis of dialkylated propanedioic acid diesters, chain-length dependent reversal of enantioselectivity, Tetrahedron 41, 1347-1352.
    • (1985) Tetrahedron , vol.41 , pp. 1347-1352
    • BjöRkling, F.1    Boutelje, J.2    Gatenbeck, S.3    Hult, K.4    Norin, T.5    Szmulik, P.6
  • 18
    • 0022398337 scopus 로고
    • Enzyme-catalyzed hydrolysis of dialkylated propanedioic acid diesters, synthesis of optically pure (S)-α-methylphenylalanine, (S)-α-methyltyrosine and (S)-α-methyl-3, 4- dihydroxyphenylalanine
    • BJÖRKLING, F., BOUTELJE, J., GATENBECK, S., HULT, K., NORIN, T. (1985b) Enzyme-catalyzed hydrolysis of dialkylated propanedioic acid diesters, synthesis of optically pure (S)-α-methylphenylalanine, (S)-α-methyltyrosine and (S)-α-methyl-3, 4- dihydroxyphenylalanine, Tetrahedron Lett. 26, 4957-4958.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 4957-4958
    • BjöRkling, F.1    Boutelje, J.2    Gatenbeck, S.3    Hult, K.4    Norin, T.5
  • 19
    • 37049077170 scopus 로고
    • Highly enantioselective route to (R)-proline derivatives via enzyme catalyzed-hydrolysis of cis-N-benzyl-2, 5-bismethoxy carbonylpyrrolidine in an aqueous dimethylsulfoxide medium
    • BJÖRKLING, F., BOUTELJE, J., HJALMARSSON, H., HULT, K., NORIN, T. (1987), Highly enantioselective route to (R)-proline derivatives via enzyme catalyzed-hydrolysis of cis-N-benzyl-2, 5-bismethoxy carbonylpyrrolidine in an aqueous dimethylsulfoxide medium, J. Chem. SOC., Chem. Commun., 1041-1042.
    • (1987) J. Chem. SOC., Chem. Commun. , pp. 1041-1042
    • BjöRkling, F.1    Boutelje, J.2    Hjalmarsson, H.3    Hult, K.4    Norin, T.5
  • 21
    • 0000598105 scopus 로고
    • Stereoselective pig-liver esterase-catalyzed hydrolysis of rigid bicyclic meso-diester - preparation of optically pure 4,7-epoxytetrahydrophtha- lides and hexa-hydrophthalides
    • BLANCO, L., GUIBÉ-JAMPEL, E., GIRARD, G. (1985), Stereoselective pig-liver esterase-catalyzed hydrolysis of rigid bicyclic meso-diester - preparation of optically pure 4,7-epoxytetrahydrophtha- lides and hexa-hydrophthalides, Tetrahedron Lett. 26, 4087-4090.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 4087-4090
    • Blanco, L.1    Guibé-Jampel, E.2    Girard, G.3
  • 22
    • 0000771029 scopus 로고
    • Application of protease-catalyzed regioselective esterification in synthesis of 6 '-deoxy-6'-fluorolactoside and 6-deoxy-6-fluorolactoside
    • CIA, S., HAKOMORI, S., TOYOKUNI, T. (1992), Application of protease-catalyzed regioselective esterification in synthesis of 6 '-deoxy-6'-fluorolactoside and 6-deoxy-6-fluorolactoside, J . Org. Chem. 57, 3431-3437.
    • (1992) J . Org. Chem. , vol.57 , pp. 3431-3437
    • Cia, S.1    Hakomori, S.2    Toyokuni, T.3
  • 23
    • 0028335627 scopus 로고
    • An efficient biocatalyzed kinetic resolution of methyl (Z)-3-arylsulphinylpropenoates
    • CARDELLICCHIO, C., NASO, F., SCILIMATI, A. (1994), An efficient biocatalyzed kinetic resolution of methyl (Z)-3-arylsulphinylpropenoates, Tetrahedron Lett. 35, 4635-4638.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4635-4638
    • Cardellicchio, C.1    Naso, F.2    Scilimati, A.3
  • 24
    • 0001404785 scopus 로고
    • An optimized sequential kinetic resolution of trans-1,2-cyclohexanediol
    • CARON, G., KAZLAUSKAS, R.J. (1991), An optimized sequential kinetic resolution of trans-1,2-cyclohexanediol, J. Org. Chem. 56, 7251-7256.
    • (1991) J. Org. Chem. , vol.56 , pp. 7251-7256
    • Caron, G.1    Kazlauskas, R.J.2
  • 25
    • 0028137574 scopus 로고
    • Peptide-synthesis catalyzed by cross-linked a-chymotrypsin in water dimethylformamide solvent system
    • CEROVSKY V., JAKUBKE, H.-D. (1994), Peptide-synthesis catalyzed by cross-linked a-chymotrypsin in water dimethylformamide solvent system, Biocatalysis 11, 233-240.
    • (1994) Biocatalysis , vol.11 , pp. 233-240
    • Cerovsky, V.1    Jakubke, H.-D.2
  • 26
    • 0000441011 scopus 로고
    • Contributions of steric, electrical, and polarizability effects in enantioselective hydrolyses with Rhizopus nigricans - a quantitative-analysis
    • CHARTON, M., ZIFFER, H. (1987), Contributions of steric, electrical, and polarizability effects in enantioselective hydrolyses with Rhizopus nigricans - a quantitative-analysis, J. Org. Chem. 52, 2400-2403.
    • (1987) J. Org. Chem. , vol.52 , pp. 2400-2403
    • CHARTON, M.1    ZIFFER, H.2
  • 27
    • 13344269574 scopus 로고
    • The synthesis of pbenzyl L-aspartate and γ-benzyl L-glutamate by enzyme-catalyzed hydrolysis
    • CHEN, S.T., WANG, K.-T. (1987), The synthesis of pbenzyl L-aspartate and γ-benzyl L-glutamate by enzyme-catalyzed hydrolysis, Synthesis, 581-582.
    • (1987) Synthesis , pp. 581-582
    • Chen, S.T.1    Wang, K.-T.2
  • 28
    • 37049083208 scopus 로고
    • Papain-catalyzed esterification of N-protected amino-acids
    • CHEN, S.T., WANG, K.-T. (1988), Papain-catalyzed esterification of N-protected amino-acids, J. Chem. Soc., Chem. Commun., 327-328.
    • (1988) J. Chem. Soc., Chem. Commun. , pp. 327-328
    • Chen, S.T.1    Wang, K.-T.2
  • 29
    • 0007661632 scopus 로고
    • Bifunctional chiral synthons via microbiological methods. 1. Optically-active 2,4-dirnethylglutaric acid monomethyl esters
    • CHEN, C.S., FUJIMOTO, Y., SIH, C.J. (1981), Bifunctional chiral synthons via microbiological methods. 1. Optically-active 2,4-dirnethylglutaric acid monomethyl esters, J. Am. Chem. Soc. 103, 3580-3582.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 3580-3582
    • Chen, C.S.1    Fujimoto, Y.2    Sih, C.J.3
  • 30
    • 20644469267 scopus 로고
    • Quantitative analyses of biochemical kinetic resolutions of enantiomers
    • CHEN, C.S., FUJIMOTO, Y., GIRDAUKAS, G., SIH, C.J. (1982), Quantitative analyses of biochemical kinetic resolutions of enantiomers, J. Am. Chem. Soc. 104, 7294-7305.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 7294-7305
    • Chen, C.S.1    Fujimoto, Y.2    Girdaukas, G.3    Sih, C.J.4
  • 31
    • 37049074382 scopus 로고
    • Chirally selective hydrolysis of D,L-amino acid-esters by alkaline protease
    • CHEN, S.-T., WANG, K.-T., WONG, C.-H. (1986). Chirally selective hydrolysis of D,L-amino acid-esters by alkaline protease, J. Chem. Soc., Chem. Commun., 1514-1516.
    • (1986) J. Chem. Soc., Chem. Commun. , pp. 1514-1516
    • Chen, S.-T.1    Wang, K.-T.2    Wong, C.-H.3
  • 32
    • 0025801245 scopus 로고
    • Diastereoselective hydrolysis of peptide esters by an alkaline protease -preparation of racemization free peptides
    • CHEN, S.-T., CHEN, S.Y., HSIAO, S.C., WANG, K.-T. (1991). Diastereoselective hydrolysis of peptide esters by an alkaline protease -preparation of racemization free peptides, Int. J. Pept. Protein Res. 37, 347.
    • (1991) Int. J. Pept. Protein Res. , vol.37 , pp. 347
    • Chen, S.-T.1    Chen, S.Y.2    Hsiao, S.C.3    Wang, K.-T.4
  • 34
    • 0026542486 scopus 로고
    • Enantioselective synthesis of (+) and (-)-cis-3-aminocyclopentane carboxylic acids by enzymatic asymmetrization
    • CHÉNEVERT, R., MARTIN, R., (1992) Enantioselective synthesis of (+) and (-)-cis-3-aminocyclopentane carboxylic acids by enzymatic asymmetrization, Tetrahedron: Asymmetry 3, 199-200.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 199-200
    • Chénevert, R.1    Martin, R.2
  • 35
    • 0015133156 scopus 로고
    • Enzymatic resolution.An organic-biochemical laboratory experiment
    • CLEMENT, G.E., POTTER, R. (1971), Enzymatic resolution.An organic-biochemical laboratory experiment, J. Chem. Educ. 48, 695-696.
    • (1971) J. Chem. Educ. , vol.48 , pp. 695-696
    • Clement, G.E.1    Potter, R.2
  • 36
    • 0014525912 scopus 로고
    • Active site and stereospecificity of a-chyrnotrypsin
    • COHEN, S.G. (1969), Active site and stereospecificity of a-chyrnotrypsin, Trans. N. Y Acad. Sci. 31, 705-719.
    • (1969) Trans. N. Y Acad. Sci. , vol.31 , pp. 705-719
    • Cohen, S.G.1
  • 37
    • 0343098074 scopus 로고
    • Requirements for stereospecificity in hydrolysis by α-chymo-trypsin. Diethyl β-acetamidoglutarate
    • COHEN, S.G., KHEDOURI, E. (1961a), Requirements for stereospecificity in hydrolysis by α-chymo-trypsin. Diethyl β-acetamidoglutarate, J. Am. Chem. Soc. 83, 1093.
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 1093
    • Cohen, S.G.1    Khedouri, E.2
  • 38
    • 0001639065 scopus 로고
    • Requirements for stereospecificity in hydrolysis by α-chymotrypsin. IV. The hydroxyl substituent. Absolute configuration
    • COHEN, S.G., KHEDOURI, E. (1961b), Requirements for stereospecificity in hydrolysis by α-chymotrypsin. IV. The hydroxyl substituent. Absolute configuration, J. Am. Chem. Soc. 83, 4228.
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 4228
    • Cohen, S.G.1    Khedouri, E.2
  • 40
    • 0029042265 scopus 로고
    • Biocatalytic resolution of a tertiary quinuclidinol ester using pig-liver esterase
    • COOPE, J.F., MAIN, B.G. (1995). Biocatalytic resolution of a tertiary quinuclidinol ester using pig-liver esterase, Tetrahedron Asymmetry 6, 1393-1398.
    • (1995) Tetrahedron Asymmetry , vol.6 , pp. 1393-1398
    • Coope, J.F.1    Main, B.G.2
  • 41
    • 37049068805 scopus 로고
    • Enzymatic-hydrolysis of (±)-trans-l,2-diacetoxycycloalkanes - a facile route to optically-active cycloalkane-1,2-diols
    • CROUT, D.H.G., GAUDET, V.S.B., LAUMEN, K., SCHEIDER, M.P. (1986), Enzymatic-hydrolysis of (±)-trans-l,2-diacetoxycycloalkanes - a facile route to optically-active cycloalkane-1,2-diols, J. Chem. Soc., Perkin Trans. 1, 808-810.
    • (1986) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 808-810
    • Crout, D.H.G.1    Gaudet, V.S.B.2    Laumen, K.3    Scheider, M.P.4
  • 42
    • 37049073724 scopus 로고
    • Applications of biotransformations in organic synthesis - preparation of enantiomerically pure esters of cis-epoxysuccinic and trans-epoxysuccinic acid
    • CROUT, D.H.G., GAUDET, V.S.B., HALLINAN, K.O. (1993), Applications of biotransformations in organic synthesis - preparation of enantiomerically pure esters of cis-epoxysuccinic and trans-epoxysuccinic acid, J. Chem. Soc. Perkin Trans. 1, 805-812.
    • (1993) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 805-812
    • Crout, D.H.G.1    Gaudet, V.S.B.2    Hallinan, K.O.3
  • 43
    • 0024560436 scopus 로고
    • Novel stereospecific silyl group transfer reaction- practical routes to the prostaglandins
    • DAMOSHEFSKY, S.J., PAZ CABAL, M., CHOW, K. (1989), Novel stereospecific silyl group transfer reaction- practical routes to the prostaglandins, J. Am. Chem. Soc. 111, 3456-3457.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 3456-3457
    • Damoshefsky, S.J.1    Paz Cabal, M.2    Chow, K.3
  • 44
    • 0000723644 scopus 로고
    • A highly enantioselective hydrolysis of cis-3,5-diacetoxycyclopent-1- ene - an enzymatic preparation of 3(R)-acetoxy- 5(S)-h ydrox ycyclopent-1 -ene
    • DEARDOREF, D.A., MATTHEWS, A.J., MCMEEKIN, D.S., CRANEY, C.L. (1986), A highly enantioselective hydrolysis of cis-3,5-diacetoxycyclopent-1- ene - an enzymatic preparation of 3(R)-acetoxy- 5(S)-h ydrox ycyclopent-1 -ene, Tetrahedron Lett. 27, 1255-1256.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 1255-1256
    • Deardoref, D.A.1    Matthews, A.J.2    Mcmeekin, D.S.3    Craney, C.L.4
  • 45
    • 0025098947 scopus 로고
    • Enzymes in organic synthesis. 6. Scope and enantioselectivity of enzymatic hydrolyses of organosilyl-substituted esters
    • DE JESO, B., BELAIR, N., DELENZE, H., RASCLE, M.-C., MAILLARD, B. ( 1990), Enzymes in organic synthesis. 6. Scope and enantioselectivity of enzymatic hydrolyses of organosilyl-substituted esters, Tetrahedron Lett. 31, 653-654.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 653-654
    • De Jeso, B.1    Belair, N.2    Delenze, H.3    Rascle, M.-C.4    Maillard, B.5
  • 46
    • 0025353766 scopus 로고
    • Enzymecatalyzed acylation of castanospermine and L-deoxynojirimycin,
    • DELINCK, D.L., MARGOLIN, A.L. (1990), Enzymecatalyzed acylation of castanospermine and L-deoxynojirimycin, Tetrahedron Lett. 31, 3093-3096.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 3093-3096
    • DElinck, D.L.1    Margolin, A.L.2
  • 47
    • 0023224952 scopus 로고
    • Novel synthesis of the aldose reductase inhibitor sorbinil via amidoalkylation, intramolecular oxazolidin- 5-one alkylation, and chymotrypsin resolution
    • DIRLAM, N.L., MOORE, B.S., URBAN, F.J. (1987), Novel synthesis of the aldose reductase inhibitor sorbinil via amidoalkylation, intramolecular oxazolidin- 5-one alkylation, and chymotrypsin resolution, J. Org. Chem. 52, 3587-3591.
    • (1987) J. Org. Chem. , vol.52 , pp. 3587-3591
    • Dirlam, N.L.1    Moore, B.S.2    Urban, F.J.3
  • 48
    • 33845278304 scopus 로고
    • Chemoenzymic synthesis of chiral furan-derivatives - useful buildingblocks for optically-active structures
    • DRUECKHAMMER, D.G., BARBAS III, C.F., NOZAKE, K., WONG, C.-H. (1988), Chemoenzymic synthesis of chiral furan-derivatives - useful buildingblocks for optically-active structures, J. Org. Chem. 53, 1607-1611.
    • (1988) J. Org. Chem. , vol.53 , pp. 1607-1611
    • Drueckhammer, D.G.1    Barbas, C.F.2    Nozake, K.3    Wong, C.-H.4
  • 49
    • 0029956172 scopus 로고    scopus 로고
    • Chemoselective removal of protecting groups from 0-glycosyl amino-acid and peptide (methoxyethoxy)ethyl esters using lipases and papain
    • EBERLING, J., BRAUN, P., KOWLCZYK, D., SCHULTZ, M., KUNZ, H. (1996), Chemoselective removal of protecting groups from 0-glycosyl amino-acid and peptide (methoxyethoxy)ethyl esters using lipases and papain, J. Org. Chem. 61, 2638-2646.
    • (1996) J. Org. Chem. , vol.61 , pp. 2638-2646
    • Eberling, J.1    Braun, P.2    Kowlczyk, D.3    Schultz, M.4    Kunz, H.5
  • 51
    • 0028566026 scopus 로고
    • Combined use of subtilisin and N-acetylneuraminic acid aldolase for the synthesis of a fluorescent sialic-acid
    • FITZ, W., WONG, C.-H. (1994), Combined use of subtilisin and N-acetylneuraminic acid aldolase for the synthesis of a fluorescent sialic-acid, J. Org. Chem. 59, 8279-8280.
    • (1994) J. Org. Chem. , vol.59 , pp. 8279-8280
    • Fitz, W.1    Wong, C.-H.2
  • 52
    • 84993914562 scopus 로고
    • Enzymatic resolution of medium-ring lactones -synthesis of ( S ) - ( + )-phoracantholide-I
    • FOUQUE, E., ROUSSEAU, G. (1989), Enzymatic resolution of medium-ring lactones -synthesis of ( S ) - ( + )-phoracantholide-I, Synthesis, 661-666.
    • (1989) Synthesis , pp. 661-666
    • Fouque, E.1    Rousseau, G.2
  • 53
    • 37049084145 scopus 로고
    • Penicillin acylase and a-chymotrypsin catalyzed hydrolysis of phenylacetate and phenylpropionate esters of 2,2-dimethyl-1,3- dioxolane-4-methanols
    • FUGANTI, C., GRASSELLI, P., SERVI, S., LAZZARINI, A., CASATI, P. (1987), Penicillin acylase and a-chymotrypsin catalyzed hydrolysis of phenylacetate and phenylpropionate esters of 2,2-dimethyl-1,3- dioxolane-4-methanols, J. Chem. Soc., Chem. Commun., 538- 539.
    • (1987) J. Chem. Soc., Chem. Commun. , pp. 538-539
    • Fuganti, C.1    Grasselli, P.2    Servi, S.3    Lazzarini, A.4    Casati, P.5
  • 54
    • 0001670962 scopus 로고
    • Substrate-specificity and enantioselectivity of penicillin acylase catalyzed hydrolysis of phenacetyl esters of synthetically useful carbinols
    • FUGANTI, C., GRASELLI, P,M SERVI, S., LAZZARINI, A., CASATI, P. (1988), Substrate-specificity and enantioselectivity of penicillin acylase catalyzed hydrolysis of phenacetyl esters of synthetically useful carbinols, Tetrahedron 44, 2575-2582.
    • (1988) Tetrahedron , vol.44 , pp. 2575-2582
    • Fuganti, C.1    Graselli, P.M.2    Servi, S.3    Lazzarini, A.4    Casati, P.5
  • 55
    • 84985534678 scopus 로고
    • Enantioselective and enantioconvergent syntheses of buildingblocks for the total synthesis of cyclopentanoid natural products
    • GAIS, H.-J., LUKAS, K.L. (1984), Enantioselective and enantioconvergent syntheses of buildingblocks for the total synthesis of cyclopentanoid natural products, Angew. Chem. (Int. Edn. Engl.) 23, 142-143.
    • (1984) Angew. Chem. (Int. Edn. Engl.) , vol.23 , pp. 142-143
    • Gais, H.-J.1    Lukas, K.L.2
  • 56
    • 0012980002 scopus 로고
    • Enzyme-catalyzed asymmetric- synthesis. 4. Synthesis of homochiral building-blocks for the enantioselective total synthesis of cyclopentanoids with an esterase-catalyzed asymmetric reaction as key step
    • GAIS, H.-J., LUKAS, K.L., BALL, W.A., BRAUN, S., LINDNER, H.J. (1986), Enzyme-catalyzed asymmetric- synthesis. 4. Synthesis of homochiral building-blocks for the enantioselective total synthesis of cyclopentanoids with an esterase-catalyzed asymmetric reaction as key step, Liebigs Ann. Chem., 687-716.
    • (1986) Liebigs Ann. Chem. , pp. 687-716
    • Gais, H.-J.1    Lukas, K.L.2    Ball, W.A.3    Braun, S.4    Lindner, H.J.5
  • 57
    • 0013563231 scopus 로고
    • Enantioselective hydrolyses by bakers' yeast. 2. Esters of N-acetyl amino-acids
    • GLÄNZER, B.I., FABER, K., GRIENGL, H. (1987a), Enantioselective hydrolyses by bakers' yeast. 2. Esters of N-acetyl amino-acids, Tetrahedron 43, 771-778.
    • (1987) Tetrahedron , vol.43 , pp. 771-778
    • GläNzer, B.I.1    Faber, K.2    Griengl, H.3
  • 58
    • 0001478678 scopus 로고
    • Enantioselective hydrolyses by bakers' yeast. 3. Microbial resolution of alkynyl esters using lyophilized yeast
    • GLÄNZER, B.I., FABER, K., GRIENGL, H. (1987b), Enantioselective hydrolyses by bakers' yeast. 3. Microbial resolution of alkynyl esters using lyophilized yeast, Tetrahedron 43, 5791-5796.
    • (1987) Tetrahedron , vol.43 , pp. 5791-5796
    • Glänzer, B.I.1    Faber, K.2    Griengl, H.3
  • 59
    • 0015245092 scopus 로고
    • Pig liver esterase reactions with alcohols, structure-reactivity correlations of the acyl-enzyme intermediate
    • GREENZAID, P,M. JENKS, W.P. (1971), Pig liver esterase reactions with alcohols, structure-reactivity correlations of the acyl-enzyme intermediate, Biochemistry 10, 1210-1222.
    • (1971) Biochemistry , vol.10 , pp. 1210-1222
    • Greenzaid, P.M.1    Jenks, W.P.2
  • 60
    • 0000288777 scopus 로고
    • Total synthesis of allosamidin - an application of the sulfonamidoglycosylation of glycals
    • GRIFFITHS, D.A., DANISHEFSKY, S.J. (1991), Total synthesis of allosamidin - an application of the sulfonamidoglycosylation of glycals, J. Am. Chem. Soc, 113, 5863-5864.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 5863-5864
    • Griffiths, D.A.1    Danishefsky, S.J.2
  • 61
    • 0002860006 scopus 로고
    • Enzymatic resolution of racemic bicyclic lactones by horse liver esterase
    • GUIBÉ-JAMPEL, E., ROUSSEAU, G., BLANCO, L. (1989). Enzymatic resolution of racemic bicyclic lactones by horse liver esterase, Tetrahedron Lett. 30, 6748.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 6748
    • Guibé-Jampel, E.1    Rousseau, G.2    Blanco, L.3
  • 62
    • 0027196612 scopus 로고
    • Substrate modification to increase the enantioselectivity of hydrolases - a route to optically-active cyclic allylic alcohols
    • GUPTA, A.K., KAZLAUSKAS, R.J. (1993), Substrate modification to increase the enantioselectivity of hydrolases - a route to optically-active cyclic allylic alcohols, Tetrahedron: Asymmetry 4, 879-888.
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 879-888
    • Gupta, A.K.1    Kazlauskas, R.J.2
  • 64
    • 0029013733 scopus 로고
    • Polyethylene-glycol monomethyl ether-modified pig-liver esterase - preparation, characterization and catalysis of enantioselective hydrolysis in water and acylation in organic solvents
    • HEISS, L., GAIS, H.-J. (1993), Polyethylene-glycol monomethyl ether-modified pig-liver esterase - preparation, characterization and catalysis of enantioselective hydrolysis in water and acylation in organic solvents, Tetrahedron Lett. 36, 3833-3836.
    • (1993) Tetrahedron Lett. , vol.36 , pp. 3833-3836
    • Heiss, L.1    Gais, H.-J.2
  • 65
    • 0020609216 scopus 로고
    • Verrucarins and roridins. 40. Syntheses of optically-active verrucarinic acid
    • HEROLD, P., MOHR, P., TAMM, C. (1983), Verrucarins and roridins. 40. Syntheses of optically-active verrucarinic acid, Helv. Chim. Acta 66,744-754.
    • (1983) Helv. Chim. Acta , vol.66 , pp. 744-754
    • Herold, P.1    Mohr, P.2    Tamm, C.3
  • 66
    • 37049079327 scopus 로고
    • Synthesis of enantiomerically pure (R)-2-sulfanylpropanoic and (S)-2-sulfanylpropanoic acids (thiolactic acid) from ethyl (S)-lactate using pig-liver esterase
    • HOF, R. P., KELLOGGR, M. (1995), Synthesis of enantiomerically pure (R)-2-sulfanylpropanoic and (S)-2-sulfanylpropanoic acids (thiolactic acid) from ethyl (S)-lactate using pig-liver esterase, J. Chem. Soc. Perkin Trans. I, 1247-1249.
    • (1995) J. Chem. Soc. Perkin Trans. I , pp. 1247-1249
    • Hof, R.P.1    Kelloggr, M.2
  • 67
    • 84956398335 scopus 로고
    • Two syntheses of 3-azido-3-deoxy-D-mannose
    • HOLLA, E. W., SINNWELL, V., KLAFFKE, W. (1992). Two syntheses of 3-azido-3-deoxy-D-mannose, Synlett, 413-414.
    • (1992) Synlett , pp. 413-414
    • Holla, E.W.1    Sinnwell, V.2    Klaffke, W.3
  • 70
    • 0000329492 scopus 로고
    • Chemoenzymatic synthesis of 2-amino-3-(2,2 ' - bipyridiny1)propanoic acids
    • IMPERIALI, B., PRINS, T. J., FISHER, S. L. (1993). Chemoenzymatic synthesis of 2-amino-3-(2,2 ' - bipyridiny1)propanoic acids, J. Org. Chem. 58 1613-1616.
    • (1993) J. Org. Chem. , vol.58 , pp. 1613-1616
    • Imperiali, B.1    Prins, T.J.2    Fisher, S.L.3
  • 71
    • 0025688176 scopus 로고
    • Papain-catalyzed hydrolysis of N-protected glycosylated amino-acid ester
    • ISHII, H., FUNABASHI, K., MIMURA, Y., INOUE, Y. (1990), Papain-catalyzed hydrolysis of N-protected glycosylated amino-acid ester, Bull. Chem. Soc. Jpn. 63,3042-3043.
    • (1990) Bull. Chem. Soc. Jpn. , vol.63 , pp. 3042-3043
    • Ishii, H.1    Funabashi, K.2    Mimura, Y.3    Inoue, Y.4
  • 72
    • 0000199517 scopus 로고
    • Chirally selective synthesis of sugar moiety of nucleosides by chemicoenzymatic approach - L-riboses and D-riboses, showdomycin, and cordycepin
    • ITO, Y., SHIBATA, T., ARITA, H., SAWAI, H., OHNO, M. (1981), Chirally selective synthesis of sugar moiety of nucleosides by chemicoenzymatic approach - L-riboses and D-riboses, showdomycin, and cordycepin, J. Am. Chem. Soc. 103,6739-6741.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 6739-6741
    • Ito, Y.1    Shibata, T.2    Arita, H.3    Sawai, H.4    Ohno, M.5
  • 73
    • 0022531498 scopus 로고
    • Triply convergent synthesis of ( -)-prostaglandin-Ez
    • JOHNSON, C. R., PENNING, T.D., (1986),Triply convergent synthesis of ( -)-prostaglandin-Ez, J. Am. Chem. Soc. 108,5655-5656.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 55-5656
    • Johnson, C.R.1    Penning, T.D.2
  • 74
    • 0024535654 scopus 로고
    • Polyhydroxylated 7-membered chiral building-blocks asymmetric-synthesis of compactin analogs
    • JOHNSON, C. R., SENANAYAKE, C. H. (1989), Polyhydroxylated 7-membered chiral building-blocks asymmetric-synthesis of compactin analogs, J. Org. Chem. 54,735-736.
    • (1989) J. Org. Chem. , vol.54 , pp. 735-736
    • JOHNSON, C.R.1    SENANAYAKE, C.H.2
  • 75
    • 0001482685 scopus 로고
    • Probing the specificity of synthetically useful enzymes
    • JONES, J. B. (1993), Probing the specificity of synthetically useful enzymes, Aldrichimica Acta 26, 105-112.
    • (1993) Aldrichimica Acta , vol.26 , pp. 105-112
    • Jones, J.B.1
  • 76
    • 0000570880 scopus 로고
    • Enzymes in organic-synthesis. 33. Stereoselective pig-liver esterase-catalyzed hydrolyses of mesocyclopentyl-1,3-diesters, tetrahydrofuranyl-l,3-diesters, and tetrahydrothiophenyl-1,3-diesters
    • JONES, J. B., HINKSR, S., HULTINP, G. (1985), Enzymes in organic-synthesis. 33. Stereoselective pig-liver esterase-catalyzed hydrolyses of mesocyclopentyl-1,3-diesters, tetrahydrofuranyl-l,3-diesters, and tetrahydrothiophenyl-1,3-diesters Can. J. Chem. 63,452-456.
    • (1985) Can. J. Chem. , vol.63 , pp. 452-456
    • Jones, J.B.1    Hinksr, S.2    Hultinp, G.3
  • 78
    • 0006432974 scopus 로고
    • Enantioselective ester hydrolyses employing Rhizopus nigricans - a method of preparing and assigning the absolute stereochemistry of cyclic alcohols
    • KASAI, M., KAWAI, K., MITSURU, I., ZIFFER, H. (1984), Enantioselective ester hydrolyses employing Rhizopus nigricans - a method of preparing and assigning the absolute stereochemistry of cyclic alcohols, J. Org. Chem. 49,675-679.
    • (1984) J. Org. Chem. , vol.49 , pp. 675-679
    • Kasai, M.1    Kawai, K.2    Mitsuru, I.3    Ziffer, H.4
  • 79
    • 84922809961 scopus 로고
    • Enantioselective ester hydrolyses using Rhizopus nigricans - stereoselective synthesis and absolute stereochemistry of ( - )-cis-l-hydroxy-4-methyl- 1,2,3,4-tetrahydronaphthalene and ( - )-rrans-1- hydroxy-4-methyl-1,2,3,4-tetrahydronaphthalene
    • KASAI, M., ZIFFEH, R., SILVERTON J. V. (1989), Enantioselective ester hydrolyses using Rhizopus nigricans - stereoselective synthesis and absolute stereochemistry of ( - )-cis-l-hydroxy-4-methyl- 1,2,3,4-tetrahydronaphthalene and ( - )-rrans-1- hydroxy-4-methyl-1,2,3,4-tetrahydronaphthalene, Can. J. Chem. 63,1287-1291.
    • (1989) Can. J. Chem. , vol.63 , pp. 1287-1291
    • Kasai, M.1    Ziffeh, R.2    Silverton, J.V.3
  • 80
    • 0000261561 scopus 로고
    • Resolution of binaphthols and spirobiindanols using cholesterol esterase
    • KAZLAUSKAS, R. J. (1989), Resolution of binaphthols and spirobiindanols using cholesterol esterase, J. Am. Chem. Soc. 111,4953-4959.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 4953-4959
    • Kazlauskas, R.J.1
  • 81
    • 84952903460 scopus 로고
    • (S)-( -) and (R) - (+ )-bi- 2-naphtho1
    • KAZLAUSKAS, R. J. (1992), (S)-( -) and (R) - (+ )-bi- 2-naphtho1, Org. Synth. 70,6047.
    • (1992) Org. Synth. , vol.70 , pp. 6047
    • Kazlauskas, R.J.1
  • 82
    • 33751499686 scopus 로고
    • A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosa
    • KAZLAUSKAS, R. J., WEISSFLOCH, A. N. E., RAPPAPORT, A.T., CUCCIA, L. A. (1991), A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosa, J. Org. Chem. 56, 2656-2665.
    • (1991) J. Org. Chem. , vol.56 , pp. 2656-2665
    • Kazlauskas, R.J.1    Weissfloch, A.N.E.2    Rappaport, A.T.3    Cuccia, L.A.4
  • 83
    • 0028361617 scopus 로고
    • Resolution of (1,l '-binaphthalene)-2,2'- dithiol by enzyme-catalyzed hydrolysis of a racemic diacyl derivative
    • KIEFER, M., VOGEL, R., HELMCHEN, G., NUBER, B. (1994), Resolution of (1,l '-binaphthalene)-2,2'- dithiol by enzyme-catalyzed hydrolysis of a racemic diacyl derivative, Tetrahedron 50, 7109-7114.
    • (1994) Tetrahedron , vol.50 , pp. 7109-7114
    • Kiefer, M.1    Vogel, R.2    Helmchen, G.3    Nuber, B.4
  • 84
    • 0028109303 scopus 로고
    • Enzymatic heteroatom chemistry. 1. Enzymatic resolution of racemic phosphinoylacetates having a stereogenic phosphorus atom,
    • KIELBASINSKI, P., ZURAWINSKI, R., PIETRUSIEWICZ, K. M., ZABLOCKA, M., MIKOLAJCZYK, M., (1994). Enzymatic heteroatom chemistry. 1. Enzymatic resolution of racemic phosphinoylacetates having a stereogenic phosphorus atom, Tetrahedron Lett. 35,7081-7084.
    • (1994) Tetrahedron Lett , vol.35 , pp. 7081-7084
    • Kielbasinski, P.1    Zurawinski, R.2    Pietrusiewicz, K.M.3    Zablocka, M.4    Mikolajczyk, M.5
  • 85
    • 0023766995 scopus 로고
    • Enzymes in carbohydrate synthesis - N-acetylneuraminic acid aldolase-catalyzed reactions and preparation of N-acetyl-2-deoxy-Dneuraminic acid-derivatives
    • KIM, M. J., HENNEN, W. J., SWEERS, H. M., WONG, C.-H. (1988), Enzymes in carbohydrate synthesis - N-acetylneuraminic acid aldolase-catalyzed reactions and preparation of N-acetyl-2-deoxy-Dneuraminic acid-derivatives, J. Am. Chem. Soc. 110,6481-6486.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 6481-6486
    • Kim, M.J.1    Hennen, W.J.2    Sweers, H.M.3    Wong, C.-H.4
  • 86
    • 33845184335 scopus 로고
    • Enzymatic resolution of racemic amines - crucial role of the solvent
    • KITAGUCHI, H., FITZPATRICK, P. A., HUBER, J. E., KLIBANOV, A. M. (1989), Enzymatic resolution of racemic amines - crucial role of the solvent, J. Am. Chem. Soc. 111,3094-3095.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 3094-3095
    • Kitaguchi, H.1    Fitzpatrick, P.A.2    Huber, J.E.3    Klibanov, A.M.4
  • 87
    • 0022380454 scopus 로고
    • Creation of novel chiral synthons with enzymes and applications to natural product synthesis. 16. Diversified synthetic approaches to the carbapenem antibiotics based on symmetrization- asymmetrization concept
    • KURIHARA, M., KAMIYAMA, K., KIOBAYASHI, S., OHNO, M. (1985), Creation of novel chiral synthons with enzymes and applications to natural product synthesis. 16. Diversified synthetic approaches to the carbapenem antibiotics based on symmetrization- asymmetrization concept, Tetrahedron Lett. 26,5831-5834.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 5831-5834
    • Kurihara, M.1    Kamiyama, K.2    Kiobayashi, S.3    Ohno, M.4
  • 88
    • 0000466328 scopus 로고
    • Enzymatic kinetic resolution of a-nitro-amethyl carboxylic acids
    • LALONDE, J. L., BERGBREITER, D. E., WONG, C.-H. (1988), Enzymatic kinetic resolution of a-nitro-amethyl carboxylic acids, J. Org. Chem. 53,2323-2327.
    • (1988) J. Org. Chem. , vol.53 , pp. 2323-2327
    • Lalonde, J.L.1    Bergbreiter, D.E.2    Wong, C.-H.3
  • 89
    • 33845376087 scopus 로고
    • Enzymes in organic-synthesis. 35. Stereoselective pig-liver esterase catalyzed hydrolyses of 3-substituted glutarate diesters - optimization of enantiomeric excess via reaction conditions control
    • LAM, L. K. P., HUI, R.A.H.F., JONES, J. B. (1986), Enzymes in organic-synthesis. 35. Stereoselective pig-liver esterase catalyzed hydrolyses of 3-substituted glutarate diesters - optimization of enantiomeric excess via reaction conditions control, J. Org. Chem. 51,2047-2050.
    • (1986) J. Org. Chem. , vol.51 , pp. 2047-2050
    • Lam, L.K.P.1    Hui, R.A.H.F.2    Jones, J.B.3
  • 90
    • 0024029746 scopus 로고
    • Enzymes in organic synthesis. 42. Investigation of the effects of the isozymal composition of pig-liver esterase on its stereoselectivity in preparative-scale ester hydrolyses of asymmetric synthetic value
    • LAM, L.K.P., BROWN, C. M., DE JESO, B., LYM, L., TOONE, E. J., JONES, J. B. (1988), Enzymes in organic synthesis. 42. Investigation of the effects of the isozymal composition of pig-liver esterase on its stereoselectivity in preparative-scale ester hydrolyses of asymmetric synthetic value, J. Am. Chem. Soc. 110,4409-4411.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 4409-4411
    • Lam, L.K.P.1    Brown, C.M.2    De Jeso, B.3    Lym, L.4    Toone, E.J.5    Jones, J.B.6
  • 91
    • 0000901926 scopus 로고
    • Enzymatic-hydrolysis of prochiral cis-l,4-diacyl-2-cyclopentene- diols - preparation of (1S,4R) and (lR.4S)-4-hydroxy- 2-cyclopentenyl derivatives, versatile building- blocks for cyclopentanoid natural products
    • LAUMEN, K., SCHNEIDER, M. (1984), Enzymatic-hydrolysis of prochiral cis-l,4-diacyl-2-cyclopentene- diols - preparation of (1S,4R) and (lR.4S)-4-hydroxy- 2-cyclopentenyl derivatives, versatile building- blocks for cyclopentanoid natural products, Tetrahedron Lett. 25,5875-5878.
    • (1994) Tetrahedron Lett. , vol.25 , pp. 5875-5878
    • Laumen, K.1    Schneider, M.2
  • 92
    • 0000881071 scopus 로고
    • Enantioselective hydrolysis of cis-l,2-diacetoxycycloalkanedimethanols - enzymatic preparation of chiral building blocks from prochiral meso-substrates
    • LAWMEN, K., SCHNEIDER, M. (1989), Enantioselective hydrolysis of cis-l,2-diacetoxycycloalkanedimethanols - enzymatic preparation of chiral building blocks from prochiral meso-substrates, Tetrahedron Lett. 26,2073-2076.
    • (1989) Tetrahedron Lett. , vol.26 , pp. 2073-2076
    • Lawmen, K.1    Schneider, M.2
  • 93
    • 37049075275 scopus 로고
    • Enzymecatalyzed hydrolysis of 3,5-cis-diacetoxy-4-transbenzyloxymethylcyclopentene and the synthesis of aristeromycin precursors
    • LEGRAND, D. M., ROBERTS, S. M. (1992), Enzymecatalyzed hydrolysis of 3,5-cis-diacetoxy-4-transbenzyloxymethylcyclopentene and the synthesis of aristeromycin precursors, J. Chem. Soc. Perkin Trans. I, 1751-1752.
    • (1992) J. Chem. Soc. Perkin Trans. I. , pp. 1751-1752
    • Legrand, D.M.1    Roberts, S.M.2
  • 94
    • 0027405034 scopus 로고
    • Enzymes in organic-chemistry. 1. Enantioselective hydrolysis of a-( acy1oxy)phosphonates by esterolytic enzymes
    • Li, Y.-F., HAMMERSCHMIDT, F. (1993), Enzymes in organic-chemistry. 1. Enantioselective hydrolysis of a-( acy1oxy)phosphonates by esterolytic enzymes, Tetrahedron: Asymmetry 4,109-120.
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 109-120
    • Li, Y.-F.1    Hammerschmidt, F.2
  • 95
    • 0000271716 scopus 로고
    • An efficient analysis of optically active D-myo-inositol 1,4.5-triphosphate
    • LUI, Y.-C., CHENC, C.-S. (1989), An efficient analysis of optically active D-myo-inositol 1,4.5-triphosphate, Tetrahedron Lett. 30,1617-1621.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 1617-1621
    • Lui, Y.-C.1    Chenc, C.-S.2
  • 96
    • 0026607951 scopus 로고
    • Enzymatic generation of planar chirality in the (arene)tricarbonylchromium series
    • MALËZIEWX, B., JAOWEN, G., SALAUN, J., HOWELL, J. A. S., PALIN, M. G. et al. (1992), Enzymatic generation of planar chirality in the (arene)tricarbonylchromium series, Tetrahedron: Asymmetry 3,375-376.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 375-376
    • MalëZiewx, B.1    Jaowen, G.2    Salaun, J.3    Howell, J.A.S.4    Palin, M.G.5
  • 97
    • 11944260951 scopus 로고
    • Enzyme-catalyzed regioselective acylation of castanospermine
    • MARGOLIN, A. L., DELINCK, D. L., WHALON, M. R. (199O), Enzyme-catalyzed regioselective acylation of castanospermine, J. Am. Chem. Soc. 112, 2849-2854.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 2849-2854
    • Margolin, A.L.1    Delinck, D.L.2    Whalon, M.R.3
  • 98
    • 0001403033 scopus 로고
    • Enzyme-mediated enantioface-differentiating hydrolysis of a-substituted cycloalkanone enol esters
    • MATSWMO, K., TSUTSWMI, S., IHORI, T., OHTA, H. (1990), Enzyme-mediated enantioface-differentiating hydrolysis of a-substituted cycloalkanone enol esters,J. Am. Chem. Soc. 112,9614-9619.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 9614-9619
    • Matswmo, K.1    Tsutswmi, S.2    Ihori, T.3    Ohta, H.4
  • 99
    • 0027390907 scopus 로고
    • Enzyme-catalyzed synthesis of optically pure P-sulfonamidopropionic acids - useful starting materials for p-3 site modified renin inhibitors
    • MAZDIYASNI, H., KONOPACKI, D. B., DICKMAN, D. A., ZYDOWSKY, T. M. (1993). Enzyme-catalyzed synthesis of optically pure P-sulfonamidopropionic acids - useful starting materials for p-3 site modified renin inhibitors, Tetrahedron Lett. 34,435-438.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 435-438.
    • Mazdiyasni, H.1    Konopacki, D.B.2    Dickman, D.A.3    Zydowsky, T.M.4
  • 101
    • 84918123834 scopus 로고
    • A study of stereoselective hydrolysis of symmetrical diesters with pig-liver esterase
    • MOHR, P., WAESPE-SARCEVIC, N., TAMM, C., GAWRONSKA, K., GAWRONSKI, J. K., (1983), A study of stereoselective hydrolysis of symmetrical diesters with pig-liver esterase, Helv. Chim. Acta 66,2501-2511.
    • (1980) Helv. Chim. Acta , vol.66 , pp. 2501-2511
    • Mohr, P.1    Waespe-Sarcevic, N.2    Tamm, C.3    Gawronska, K.4    Gawronski, J.K.5
  • 102
    • 84987553189 scopus 로고
    • 3-Hydroxyglutarate and P-epoxy, y-epoxy esters as substrates for pig-liver esterase (ple) and a-chymotrypsin
    • MOHRl, P., RÖSSLEIN, L., TAMM, C. (1987). 3-Hydroxyglutarate and P-epoxy, y-epoxy esters as substrates for pig-liver esterase (ple) and a-chymotrypsin, Helv. Chim. Acta 70,142-152.
    • (1987) Helv. Chim. Acta , vol.70 , pp. 142-152
    • Mohrl, P.1    RöSslein, L.2    Tamm, C.3
  • 103
    • 0029029076 scopus 로고
    • Bile salt-moddated stereoselection in the cholesterol esterasecatalyzed hydrolysis of a-tocopheryl acetates
    • MOORE, A. N. J., DUTTIN, P. J., ZAHALKA, H. A., BURTON, G. W., INGOLD, K. U. (1995). Bile salt-moddated stereoselection in the cholesterol esterasecatalyzed hydrolysis of a-tocopheryl acetates, J. Am. Chem. Soc. 117,5677-5686.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5677-5686
    • Moore, A.N.J.1    Duttin, P.J.2    Zahalka, H.A.3    Burton, G.W.4    Ingold, K.U.5
  • 104
    • 0025895521 scopus 로고
    • Ple catalyzed hydrolyses of a-substituted a-hydroxy esters - the influence of the substituents
    • MOORLAG, H., KELLOGG, R. M. (1991), Ple catalyzed hydrolyses of a-substituted a-hydroxy esters - the influence of the substituents, Tetrahedron: Asymmetry 2,705-720.
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 705-720
    • Moorlag, H.1    Kellogg, R.M.2
  • 106
    • 0001882204 scopus 로고
    • Synthesis of optically active alkynyl alcohols and a-hydroxy esters by microbial asymmetric hydrolysis of the corresponding acetate
    • MORI, K., AKAO, H. (1980a), Synthesis of optically active alkynyl alcohols and a-hydroxy esters by microbial asymmetric hydrolysis of the corresponding acetate, Tetrahedron 36,91-96.
    • (1980) Tetrahedron , vol.36 , pp. 91-96
    • Mori, K.1    Akao, H.2
  • 107
    • 0019164635 scopus 로고
    • Preparation of both enantiomers of threo-2-amino-3-methylhexanoic acid by enzymatic resolution and their conversion to optically active forms of threo-4-methylheptan- 3-01, a pheromone component of smaller European elm bark beetle
    • MORI, K., AKAO, H. (1980b), Preparation of both enantiomers of threo-2-amino-3-methylhexanoic acid by enzymatic resolution and their conversion to optically active forms of threo-4-methylheptan- 3-01, a pheromone component of smaller European elm bark beetle. Tetrahedron 36, 2209-2213.
    • (1980) Tetrahedron , vol.36 , pp. 2209-2213
    • Mori, K.1    Akao, H.2
  • 108
    • 37049067041 scopus 로고
    • Synthesis and enantiomer recognition of crown ethers containing cyclohexane-1,2-diol derivatives as the chiral center and enzymatic resolution of the chiral subunits,
    • NAEMURA, K., MIYABE, H., SHINGAI, Z.(1991), Synthesis and enantiomer recognition of crown ethers containing cyclohexane-1,2-diol derivatives as the chiral center and enzymatic resolution of the chiral subunits, J. Chem. Soc. Perkin Trans. I, 957-959.
    • (1991) J. Chem. SOC. Perkin Trans. , vol.1 , pp. 957-959
    • Naemura, K.1    Miyabe, H.2    Shingai, Z.3
  • 109
    • 37049073629 scopus 로고
    • Resolution of the diols of bicyclo[2.2.l]heptane, bicyclo[2.2.2]octane and bicyclo[3.2.l]octane by enzymatic hydrolysis, and their absolute-configurations
    • NAEMURA, K., TAKAHASHI, N. TANAKA, S. (1992). Resolution of the diols of bicyclo[2.2.l]heptane, bicyclo[2.2.2]octane and bicyclo[3.2.l]octane by enzymatic hydrolysis, and their absolute-configurations, J. Chem. Soc. Perkin Trans. I, 2337-2343.
    • (1992) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2337-2343
    • Naemura, K.1    Takahashi, N.2    Tanaka, S.3
  • 110
    • 0027159502 scopus 로고
    • Enzyme-catalyzed asymmetric acylation and hydrolysis of cis- 2.5-disubstituted tetrahydrofuran derivatives - contribution to development of models for reactions catalyzed by porcine liver esterase and porcine pancreatic lipase
    • NAEMWRA, K., FUKUDA, R., TAKAHASHI, N., KONISHI, M., HIROSE, Y., TOBE, Y. (1993). Enzyme-catalyzed asymmetric acylation and hydrolysis of cis- 2.5-disubstituted tetrahydrofuran derivatives - contribution to development of models for reactions catalyzed by porcine liver esterase and porcine pancreatic lipase, Tetrahedron: Asymmetry 4,911-918.
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 911-918
    • Naemwra, K.1    Fukuda, R.2    Takahashi, N.3    Konishi, M.4    Hirose, Y.5    Tobe, Y.6
  • 111
    • 0011007821 scopus 로고
    • The kinetics of the a-chymotrypsin catalyzed hydrolysis of acetyl- and nicotinyl-L-tryptophanamide in aqueous solution at 25°C and pH 7.9
    • NIEMANN, C., HUANG, H. T. (1951), The kinetics of the a-chymotrypsin catalyzed hydrolysis of acetyl- and nicotinyl-L-tryptophanamide in aqueous solution at 25°C and pH 7.9, J. Am. Chem. Soc. 73 1541-1548.
    • (1991) J. Am. Chem. Soc. , vol.73 , pp. 1541-1548
    • Niemann, C.1    Huang, H.T.2
  • 112
    • 0345760512 scopus 로고
    • The kinetics of the a-chymotrypsin catalyzed hydrolysis of acetyl-L-tyrosinamide in aqueous solutions at 25°C and pH 7.8-8.0
    • NIEMANN, C., THOMAS, D. W., MACALLISTER, R. V. (1951), The kinetics of the a-chymotrypsin catalyzed hydrolysis of acetyl-L-tyrosinamide in aqueous solutions at 25°C and pH 7.8-8.0, J. Am. Chem. Soc. 73,1548
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 1548
    • Niemann, C.1    Thomas, D.W.2    Macallister, R.V.3
  • 113
    • 0002203126 scopus 로고
    • Chiral synthons by ester hydrolysis catalysed by pig liver esterase
    • OHNO, M., OTSUKA, M. (1989), Chiral synthons by ester hydrolysis catalysed by pig liver esterase, Org. React. 37, l-250.
    • (1989) Org. React. , vol.37 , pp. l-250
    • Ohno, M.1    Otsuka, M.2
  • 114
    • 0019406481 scopus 로고
    • Synthesis of (S)-4-[(methoxycarbonyl) methyl]-2-azetidinone and (R)-4-[(methoxycarbonyl) methyl]-2-azetidinone by chemicoenzymatic approach
    • OHNO, M., KOBAYASHI, S., IIMORI, T., WONG, Y.-F., IZAWA, T. (1981), Synthesis of (S)-4-[(methoxycarbonyl) methyl]-2-azetidinone and (R)-4-[(methoxycarbonyl) methyl]-2-azetidinone by chemicoenzymatic approach, J. Am. Chem. Soc. 103, 2405-2406.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 2405-2406
    • Ohno, M.1    Kobayashi, S.2    Iimori, T.3    Wong, Y.-F.4    Izawa, T.5
  • 115
    • 0006884780 scopus 로고
    • Microbial synthesis of optically pure a-methoxy-a-trifluoromethyl- a-phenylacetic acid
    • OHTA, H., MIYAMAE, Y., KIMURA, Y. (1989a), Microbial synthesis of optically pure a-methoxy-a-trifluoromethyl- a-phenylacetic acid, Chem Lett., 379-380.
    • (1989) Chem Lett. , pp. 379-380
    • Ohta, H.1    Miyamae, Y.2    Kimura, Y.3
  • 116
    • 0001639775 scopus 로고
    • Enzymatic kinetic resolution of cyanohydrin acetates and its application to the synthesis of (S)-(-)frontalin
    • OHTA, H., KIMURA, Y., SUGANO, Y., SUGAI, T. (1989b), Enzymatic kinetic resolution of cyanohydrin acetates and its application to the synthesis of (S)-( - )frontalin, Tetruhedron 45, 5469-5476.
    • (1989) Tetruhedron , vol.45 , pp. 5469-5476
    • Ohta, H.1    Kimura, Y.2    Sugano, Y.3    Sugai, T.4
  • 121
    • 0001203360 scopus 로고
    • Total synthesis of (-)-chorismic acid and (- )-shikimic acid
    • PAWLAK, J. L., BERCHTOLD, G. A. (1987), Total synthesis of (-)-chorismic acid and (- )-shikimic acid, J. Org. Chem. 52,1765-1771.
    • (1987) J. Org. Chem. , vol.52 , pp. 1765-1771
    • Pawlak, J.L.1    Berchtold, G.A.2
  • 123
    • 0024356997 scopus 로고
    • Stereocontrolled functionalization of cycloheptadiene using organometallic chemistry - synthesis of the (+ )-Prelog Djerassi lactone and a tylosin subunit
    • PEARSON, A. J., LAI, Y.-S., Lu, W., PINKERTON, A. A. (1989), Stereocontrolled functionalization of cycloheptadiene using organometallic chemistry - synthesis of the (+ )-Prelog Djerassi lactone and a tylosin subunit, J. Org. Chem. 54,3882-3893.
    • (1989) J. Org. Chem. , vol.54 , pp. 3882-3893
    • Pearson, A.J.1    Lai, Y.-S.2    Lu, W.3    Pinkerton, A.A.4
  • 124
    • 0028968555 scopus 로고
    • Enhancement of the enantioselectivity of penicillin-G acylase from Escherichia coli by substrate tuning
    • POHL, T., WALDMANN, H. (1995), Enhancement of the enantioselectivity of penicillin-G acylase from Escherichia coli by substrate tuning, Tetrahedron Lett. 36,2963-2966.
    • (1955) Tetrahedron Lett. , vol.36 , pp. 2963-2966
    • Pohl, T.1    Waldmann, H.2
  • 125
    • 0025035608 scopus 로고
    • Specific esterase activity of subtilisin toward esters of a-haloacids
    • PUGNIèRE, M., SAN JUAN, C., PREVIERO, A. (1990), Specific esterase activity of subtilisin toward esters of a-haloacids, Tetrahedron Lett. 31, 4883-4886.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 4883-4886
    • PugnièRe, M.1    San Juan, C.2    Previero, A.3
  • 126
    • 37049066862 scopus 로고
    • Enantiomerically selective pig-liver esterase-catalyzed hydrolyses of racemic allenic esters
    • RAMASWANY, S., HUI, R. A. H. F., JONES, J. B. (1986), Enantiomerically selective pig-liver esterase-catalyzed hydrolyses of racemic allenic esters, J. Chem. Soc., Chem. Commun., 1545-1546.
    • (1986) J. Chem. Soc., Chem. Commun. , pp. 1545-1546
    • Ramaswany, S.1    Hui, R.A.H.F.2    Jones, J.B.3
  • 127
    • 0027371777 scopus 로고
    • Stereoselective hydrolysis of dimethyl aziridin-2,3-dicarboxylates with pig-liver esterase (PLE)
    • RENOLD, T., TAMM, C., (1993), Stereoselective hydrolysis of dimethyl aziridin-2,3-dicarboxylates with pig-liver esterase (PLE), Tetrahedron: Asyrnrnetr 4,2295-2298.
    • (1993) Tetrahedron: Asyrnrnetr , vol.4 , pp. 2295-2298
    • Renold, T.1    Tamm, C.2
  • 128
    • 33845280481 scopus 로고
    • Protease-catalyzed regioselective esterification of sugars and related-compounds in anhydrous dimethylformamide
    • RIVA, S., CHOPINEAU, J., KIEBOOM, A. P. G., KLIBANOV, A. M. (1988), Protease-catalyzed regioselective esterification of sugars and related-compounds in anhydrous dimethylformamide, J. Am. Chem. Soc. 110,584-589.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 584-589
    • Riva, S.1    Chopineau, J.2    Kieboom, A.P.G.3    Klibanov, A.M.4
  • 129
    • 85004804006 scopus 로고
    • Synthesis of phenylalanines in high enantiomeric excess via enzymatic resolution
    • ROPER, J. M., BAUER, D. P. (1983), Synthesis of phenylalanines in high enantiomeric excess via enzymatic resolution, Synthesis, 1041-1043.
    • (1983) Synthesis , pp. 1041-1043
    • Roper, J.M.1    Bauer, D.P.2
  • 130
    • 33845283189 scopus 로고
    • Enzymes in organic-synthesis. 39. Preparations of chiral cyclic acidesters and bicyclic lactones via stereoselective pig-liver esterase-catalyzed hydrolyses of cyclic meso-diesters
    • SABBIONI, G., JONES, J. B. (1987), Enzymes in organic-synthesis. 39. Preparations of chiral cyclic acidesters and bicyclic lactones via stereoselective pig-liver esterase-catalyzed hydrolyses of cyclic meso-diesters, J. Org. Chem. 52,4565-4570.
    • (1987) J. Org. Chem. , vol.52 , pp. 4565-4570
    • Sabbioni, G.1    Jones, J.B.2
  • 131
    • 84985609364 scopus 로고
    • Enzymatic syntheses of chiral building blocks from racemates - preparation of (lR,3R)-chrysanthemic, (lR,3R)-perrnethrinic and (1R,3R)- caronic acids from racemic, diastereomeric mixtures
    • SCHNEIDER, M., ENGEL, N., BOENSMANN, H., (1984a), Enzymatic syntheses of chiral building blocks from racemates - preparation of (lR,3R)-chrysanthemic, (lR,3R)-perrnethrinic and (1R,3R)- caronic acids from racemic, diastereomeric mixtures, Angew Chem. (Int. Edn. Engl.) 23,6446.
    • (1984) Angew Chem. (Int. Edn. Engl.) , vol.23 , pp. 6446
    • Schneider, M.1    Engel, N.2    Boensmann, H.3
  • 132
    • 84985544969 scopus 로고
    • Hydrolytic enzymes in organic-synthesis. 3. Enzymatic syntheses of chiral building-blocks from prochiral mesosubstrates - preparation of methyl(hydr0gen)- 1,2-~ycloalkanedicarboxylates
    • SCHNEIDER, M., ENGEL, N., HONICKE, P., HEINEMANN, G., GORISCH, H. (1984b), Hydrolytic enzymes in organic-synthesis. 3. Enzymatic syntheses of chiral building-blocks from prochiral mesosubstrates - preparation of methyl(hydr0gen)- 1,2-~ycloalkanedicarboxylates, Angew. Chem. (Int. Edn. Engl.) 23,6748.
    • (1984) Angew. Chem. (Int. Edn. Engl.) , vol.23 , pp. 6748
    • Schneider, M.1    Engel, N.2    Honicke, P.3    Heinemann, G.4    Gorisch, H.5
  • 133
    • 0022839369 scopus 로고
    • Total synthesis of the macrodiolide (+)-Conglobatin
    • SCHREGENBERGER, C., SEEBACH, D. (1986), Total synthesis of the macrodiolide (+)-Conglobatin, Liebigs Ann. Chem., 2081-2103.
    • (1986) Liebigs Ann. Chem. , pp. 2081-2103
    • Schregenberger, C.1    Seebach, D.2
  • 134
    • 0026662593 scopus 로고
    • a-Chymotrypsin catalyzed enantioselective hydrolysis of alkenyl-a-amino acid-esters
    • SCHRICKER, B., THIRRING, K., BERNER, H. (1992), a-Chymotrypsin catalyzed enantioselective hydrolysis of alkenyl-a-amino acid-esters, Bioorg. Med. Chem. Lett. U,38 7-390.
    • (1992) Bioorg. Med. Chem. Lett. , vol.12 , pp. 387-390
    • Schricker, B.1    Thirring, K.2    Berner, H.3
  • 135
    • 0004020909 scopus 로고
    • Enantioselective cleavage of meso-nitrodiol diacetates by an esterase concentrate from fresh pig-liver - preparation of useful nitroaliphatic building-blocks for EPC syntheses
    • SEEBACH, D., EBERLE, M. (1986), Enantioselective cleavage of meso-nitrodiol diacetates by an esterase concentrate from fresh pig-liver - preparation of useful nitroaliphatic building-blocks for EPC syntheses, Chimia 40,315-318.
    • (1986) Chimia , vol.40 , pp. 315-318
    • Seebach, D.1    Eberle, M.2
  • 136
    • 0001318830 scopus 로고
    • Kinetic resolution of phosphines and phosphine oxides with phosphorus stereocenters by hydrolases
    • SERREOI, A. N., KAZLAUSKAS, R. J. (1994), Kinetic resolution of phosphines and phosphine oxides with phosphorus stereocenters by hydrolases, J. Org. Chem. 59,7609-7615.
    • (1994) J. Org. Chem. , vol.59 , pp. 7609-7615
    • Serreoi, A.N.1    Kazlauskas, R.J.2
  • 137
    • 84952947682 scopus 로고
    • Very selective enzymatic-hydrolysis of a-ester of dimethyl a-dehydroglutamate with papain
    • SHIN, C., TAKAHASHI, N., YONEZAWA, Y., (1988), Very selective enzymatic-hydrolysis of a-ester of dimethyl a-dehydroglutamate with papain, Chem. Lett., 2001-2002.
    • (1988) Chem. Lett. , pp. 2001-2002
    • Shin, C.1    Takahashi, N.2    Yonezawa, Y.3
  • 138
    • 0343045298 scopus 로고
    • Novel and selective enzymatic-hydrolysis of y-ester of dimethyl a-dehydroglutamate with a-chymotrypsin
    • SHIN, C., SEKI, M., TAKAHASHI, N.,(1990). Novel and selective enzymatic-hydrolysis of y-ester of dimethyl a-dehydroglutamate with a-chymotrypsin, Chem. Lett., 2089-2090.
    • (1990) Chem. Lett. , pp. 2089-2090
    • Shin, C.1    Seki, M.2    Takahashi, N.3
  • 139
    • 0007669055 scopus 로고
    • Dehydrooligopeptides. 13. Selective enzymatic hydrolysis of N-protected a-dehydroglutamic acid diesters and their analogs using papain as catalyst
    • SHIN, C., TAKAHASHI, N., SEKI, M. (1991), Dehydrooligopeptides. 13. Selective enzymatic hydrolysis of N-protected a-dehydroglutamic acid diesters and their analogs using papain as catalyst, Bull. Chem. Soc. Jpn. 64,3575-3580.
    • (1991) Bull. Chem. Soc. Jpn. , vol.64 , pp. 3575-3580
    • Shin, C.1    Takahashi, N.2    Seki, M.3
  • 140
    • 0029591661 scopus 로고
    • Dehydrooligopeptides. 18. Enzymatic hydrolysis and coupling of dehydrodipeptide esters containing a-dehydroamino acid residue by using papain
    • SHIN, C., KAKUSHO, T., ARAI, K., SEKI, M. (1995), Dehydrooligopeptides. 18. Enzymatic hydrolysis and coupling of dehydrodipeptide esters containing a-dehydroamino acid residue by using papain, Bull. Chem. Soc. Jpn. 68,3549-3555.
    • (1995) Bull. Chem. Soc. Jpn. , vol.68 , pp. 3549-3555
    • Shin, C.1    Kakusho, T.2    Arai, K.3    Sek I., M.4
  • 141
    • 0023185132 scopus 로고
    • Chemoenzymatic approach to carbocyclic analogs of ribonucleosides and nicotinamide ribose
    • SICSIC, S., IKBAL, M., LE GOFFIC, F. (1987), Chemoenzymatic approach to carbocyclic analogs of ribonucleosides and nicotinamide ribose, Tetrahedron Lett. 28,1887-1888.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 1887-1888
    • Sicsic, S.1    Ikbal, M.2    Le Goffic, F.3
  • 142
    • 0026680754 scopus 로고
    • Optically active compounds via biocatalytic methods
    • SIH, C. J., GU, Q. M., HOLDGRUN, X., HARRIS, K. (1992). Optically active compounds via biocatalytic methods, Chirality 4, 91-97.
    • (1992) Chirality , vol.4 , pp. 91-97
    • Sih C.J.Gu, Q.M.1    Holdgrun, X.2    Harris, K.3
  • 143
    • 0023546553 scopus 로고
    • Regioselective enzymic-hydrolysis in the isolation of isomers of Mupirocin
    • SIME, J. T., POOL, C. R., TYLER, J. W. (1987), Regioselective enzymic-hydrolysis in the isolation of isomers of Mupirocin, Tetrahedron Lett. 28, 5169-5172.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 5169-5172
    • Sime, J.T.1    Pool, C.R.2    Tyler, J.W.3
  • 145
    • 4243077546 scopus 로고
    • Bifunctional chiral synthons via microbiological methods. 2. Optically-active a-hydroxy aldehydes
    • TAKAISHI, Y., YANG, Y.-L., DITULLIO, D., SIH, C. J. (1982), Bifunctional chiral synthons via microbiological methods. 2. Optically-active a-hydroxy aldehydes. Tetrahedron Lett. 23,5489-5492.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 5489-5492
    • Takaishi, Y.1    Yang, Y.-L.2    Ditullio, D.3    Sih, C.J.4
  • 146
    • 84952903043 scopus 로고    scopus 로고
    • The 107th Annual Meeting
    • Pharmaceutical Society of Japan
    • TANAKA, S., OHAISHI, H., SUEMUNE, H., SAKAI, K. (1987), at The 107th Annual Meeting, Pharmaceutical Society of Japan.
    • Tanaka, S.1    Ohaishi, H.2    Suemune, H.3    Sakai, K.4
  • 148
    • 0025828981 scopus 로고
    • Enzymes in organic synthesis. 49. Resolutions of racemic monocyclic esters with pig-liver esterase
    • TOONE, E. J., JONES, J. B. (1991a), Enzymes in organic synthesis. 49. Resolutions of racemic monocyclic esters with pig-liver esterase, Tetrahedron: Asymmetry 2,207-222.
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 207-222
    • Toone, E.J.1    Jones, J.B.2
  • 149
    • 0026072363 scopus 로고
    • Enzymes in organic synthesis. 50. Probing the dimensions of the large hydrophobic binding region of the active-site of pig-liver esterase using substituted aryl malonate substrates
    • TOONE, E. J., JONES, J. B. (1991b), Enzymes in organic synthesis. 50. Probing the dimensions of the large hydrophobic binding region of the active-site of pig-liver esterase using substituted aryl malonate substrates, Tetrahedron: Asymmetry 2,1041-1052.
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 1041-1052
    • Toone, E.J.1    Jones, J.B.2
  • 150
    • 0025100296 scopus 로고
    • Enzymes in organic synthesis. 47. Active-site model for interpreting and predicting the specificity of pig-liver esterase
    • TOONE, E. J., WERTH, M. J., JONES, J. B. (1990), Enzymes in organic synthesis. 47. Active-site model for interpreting and predicting the specificity of pig-liver esterase, J. Am. Chem. Soc. 112, 4946-4952.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 4946-4952
    • Toone, E.J.1    Werth, M.J.2    Jones, J.B.3
  • 151
    • 0027415816 scopus 로고
    • Resolution of methyl cis-3-chloromethyl-2-tetrahydrofuran carboxylate via enzymatic hydrolysis
    • UDDING, J. H., FRAANJE, J., GOUBITZ, K., HIEMSTRA, H., SPECKAMP, W. N. (1993), Resolution of methyl cis-3-chloromethyl-2-tetrahydrofuran carboxylate via enzymatic hydrolysis, Tetrahedron: Asymmetry 4, 425-432.
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 425-432
    • Udding, J.H.1    Fraanje, J.2    Goubitz, K.3    Hiemstra, H.4    Speckamp, W.N.5
  • 152
    • 0024391175 scopus 로고
    • Regioselective deprotection of 3 ', 5 '- 0-acylated pyrimidine nucleosides by lipase and esterase
    • UEMURA, A., NOZAKI, K., YAMASHITA, J., YASUMOTO, M. (1989), Regioselective deprotection of 3 ', 5 '- 0-acylated pyrimidine nucleosides by lipase and esterase, Tetrahedron Lett. 30,3819-3820.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 3819-3820
    • Uemura, A.1    Nozaki, K.2    Yamashita, J.3    Yasumoto, M.4
  • 153
    • 84985204874 scopus 로고
    • The phenylacetyl (PHAC) group as enzymatically removable protecting function for peptides and carbohydrates - selective deprotections with penicillin acylase
    • WALDMANN, H. (1988). The phenylacetyl (PHAC) group as enzymatically removable protecting function for peptides and carbohydrates - selective deprotections with penicillin acylase, Liebigs Ann. Chem., 1175-1180.
    • (1988) Liebigs Ann. Chem. , pp. 1175-1180
    • Waldmann, H.1
  • 154
    • 0001313089 scopus 로고
    • A new access to chiral2-furylcarbinols by enantioselective hydrolysis with penicillin acylase
    • WALDMANN, H., (1989), A new access to chiral2-furylcarbinols by enantioselective hydrolysis with penicillin acylase, Tetrahedron Lett. 30,3057-3058.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 3057-3058
    • Waldmann, H.1
  • 155
    • 0025082964 scopus 로고
    • Enzymes as synthetic catalysts - mechanistic and active-site considerations of natural and modified chymotrypsin,
    • WEST, J. B., HENNEN, W. J., LALONDE, J. L., BIBBS, J. A., ZHONG, Z. et al. (1990), Enzymes as synthetic catalysts - mechanistic and active-site considerations of natural and modified chymotrypsin, J. Am. Chem. Soc. 112,5313-5320.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 5313-5320
    • West, J.B.1    Hennen, W.J.2    Lalonde, J.L.3    Bibbs, J.A.4    Zhong, Z.5
  • 156
    • 0027442373 scopus 로고
    • PLE-catalyzed resolution of a-substituted P-ketoesters, application to the synthesis of ( + )- nitramine and ( - )-isonitratnine
    • WESTERMANN, B., SCHARMANN, H. G., KARTMANN, I., (1993), PLE-catalyzed resolution of a-substituted P-ketoesters, application to the synthesis of ( + )- nitramine and ( - )-isonitratnine, Tetrahedron: Asymmetry 4,2119-2122.
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 2119-2122
    • Westermann, B.1    Scharmann, H.G.2    Kartmann, I.3
  • 157
    • 0021052681 scopus 로고
    • Enantioselective hydrolysis of 3-hydroxy-3-methylalkanoica cid esters with pig-liver esterase
    • WILSON, W. K., BACA, S. B., BARBER, Y. J., SCALLEN, T. J., MORROW, C. J. (1983), Enantioselective hydrolysis of 3-hydroxy-3-methylalkanoica cid esters with pig-liver esterase, J. Org. Chem. 48,3960-3966.
    • (1983) J. Org. Chem. , vol.48 , pp. 3960-3966
    • Wilson, W.K.1    Baca, S.B.2    Barber, Y.J.3    Scallen, T.J.4    Morrow, C.J.5
  • 158
    • 0343531747 scopus 로고
    • Preparation of optically pure N-tert-butyloxycarbonyl- 0-benzyl-L-serine and its antipode
    • WONG, C.-H., Ho, M.-F., WANG, K.-T. (1978), Preparation of optically pure N-tert-butyloxycarbonyl- 0-benzyl-L-serine and its antipode, J. Org. Chem. 43,3604-3610.
    • (1978) J. Org. Chem. , vol.43 , pp. 3604-3610
    • Wong, C.-H.1    Ho, M.-F.2    Wang, K.-T.3
  • 159
    • 0025264347 scopus 로고
    • Enzymes in organic synthesis - use of subtilisin and a highly stable mutant derived from multiple site-specific mutation
    • WONG, C.-H., CHEN, S.-T., HENNEN, W. J., BIBBS, J. A., WANG, Y.-F. et al. (1990), Enzymes in organic synthesis - use of subtilisin and a highly stable mutant derived from multiple site-specific mutation, J. Am. Chem. Soc. 112,945-953.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 945-953
    • Wong, C.-H.1    Chen, S.-T.2    Hennen, W.J.3    Bibbs, J.A.4    Wang, Y.-F.5
  • 160
    • 0028094181 scopus 로고
    • A highly regioselective esterase from Penicillium frequentans IMI- 92265
    • WORONIECKI, S. R., ARMITAGE, P. A., ELSON, S. W., FORD, B. D., SIME, J. T. (1994), A highly regioselective esterase from Penicillium frequentans IMI- 92265, Biocatalysis 8,309-320.
    • (1994) Biocatalysis , vol.8 , pp. 309-320
    • Woroniecki, S.R.1    Armitage, P.A.2    Elson, S.W.3    Ford, B.D.4    Sime, J.T.5
  • 161
    • 0025032799 scopus 로고
    • Applications of pig-liver esterases (ple) in asymmetric synthesis
    • ZHU, L.-M., TEDFORD, M. C. (1990), Applications of pig-liver esterases (ple) in asymmetric synthesis, Tetrahedron 46, 6587-6611.
    • (1990) Tetrahedron , vol.46 , pp. 6587-6611
    • Zhu, L.-M.1    Tedford, M.C.2
  • 162
    • 0000231743 scopus 로고
    • Microbially mediated enantioselective ester hydrolyses utilizing Rhitopus nigricans - a new method of assigning the absolute stereochemistry of acyclic 1-arylalkanols
    • ZIWER, H., KASAI, K., IMUTA, M., FROUSSIOS, C. (1983), Microbially mediated enantioselective ester hydrolyses utilizing Rhitopus nigricans - a new method of assigning the absolute stereochemistry of acyclic 1-arylalkanols, J. Org. Chem. 48,3017-3021.
    • (1983) J. Org. Chem. , vol.48 , pp. 3017-3021
    • Ziwer, H.1    Kasai, K.2    Imuta, M.3    Froussios, C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.