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Volumn 35, Issue 6-7, 2004, Pages 574-580

Resolution of 1,3-dioxolane derivatives using the lipase from an Acinetobacter junii SY-01

Author keywords

1,3 Dioxolane; Acinetobacter junii; Enantioselective lipase; Resolution

Indexed keywords

ENANTIOSELECTIVITY; SUBSTRATE CONCENTRATION;

EID: 7544234628     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.enzmictec.2004.08.009     Document Type: Conference Paper
Times cited : (11)

References (26)
  • 1
    • 4243101632 scopus 로고
    • FDA issues flexible policy on chiral drugs
    • S. Borman FDA issues flexible policy on chiral drugs Chem. Eng. News 6 1992 5 6
    • (1992) Chem. Eng. News , vol.6 , pp. 5-6
    • Borman, S.1
  • 2
    • 0009775884 scopus 로고
    • Chiral drugs: The coming revolution
    • D.H. Deutsch Chiral drugs: the coming revolution Chemtech 3 1991 157 159
    • (1991) Chemtech , vol.3 , pp. 157-159
    • Deutsch, D.H.1
  • 3
    • 0002312023 scopus 로고
    • Drug chirality-scale-up, manufacturing, and control
    • H.J. Federsel Drug chirality-scale-up, manufacturing, and control Chemtech 12 1993 24 33
    • (1993) Chemtech , vol.12 , pp. 24-33
    • Federsel, H.J.1
  • 4
    • 0029968911 scopus 로고    scopus 로고
    • Drug chirality: A consideration of the significance of the stereochemistry of antimicrobial agents
    • A.J. Hutt, and J. O'Grady Drug chirality: a consideration of the significance of the stereochemistry of antimicrobial agents J. Antimicrob. Chemotherap. 37 1996 7 32
    • (1996) J. Antimicrob. Chemotherap. , vol.37 , pp. 7-32
    • Hutt, A.J.1    O'Grady, J.2
  • 5
    • 33749942544 scopus 로고
    • Chiral drugs
    • S. Stinson Chiral drugs Chem. Eng. News 72 38 1994 38 72
    • (1994) Chem. Eng. News , vol.72 , Issue.38 , pp. 38-72
    • Stinson, S.1
  • 6
    • 0003735680 scopus 로고    scopus 로고
    • Counting on chiral drugs
    • S. Stinson Counting on chiral drugs Chem. Eng. News 76 38 1998 83 104
    • (1998) Chem. Eng. News , vol.76 , Issue.38 , pp. 83-104
    • Stinson, S.1
  • 7
    • 0002341111 scopus 로고    scopus 로고
    • Chiral pharmaceuticals
    • S. Stinson Chiral pharmaceuticals Chem. Eng. News 79 40 2001 79 97
    • (2001) Chem. Eng. News , vol.79 , Issue.40 , pp. 79-97
    • Stinson, S.1
  • 8
    • 0000714772 scopus 로고
    • Enzymes in organic synthesis
    • J.B. Jones Enzymes in organic synthesis Tetrahedron 42 1986 3351 3403
    • (1986) Tetrahedron , vol.42 , pp. 3351-3403
    • Jones, J.B.1
  • 9
    • 0027588112 scopus 로고
    • Enzymes in the synthesis of chiral drugs
    • A. Margolin Enzymes in the synthesis of chiral drugs Enzyme Microb. Technol. 15 1993 266 280
    • (1993) Enzyme Microb. Technol. , vol.15 , pp. 266-280
    • Margolin, A.1
  • 10
    • 0028922019 scopus 로고
    • Enantioselective hydrolysis of ethyl 2-hydroxyalkanoates by an extracellular esterase from a Bacillus sphaericus strain
    • A.J. Michael, P.L. David, and A.B. Lynne Enantioselective hydrolysis of ethyl 2-hydroxyalkanoates by an extracellular esterase from a Bacillus sphaericus strain Enzyme Microb. Technol. 17 1995 175 179
    • (1995) Enzyme Microb. Technol. , vol.17 , pp. 175-179
    • Michael, A.J.1    David, P.L.2    Lynne, A.B.3
  • 11
    • 4243794106 scopus 로고
    • The biocatalytic approach to the preparation of enantiomerically pure chiral building blocks
    • E. Santoniello, P. Ferraloschi, P. Grisent, and A. Monzouchi The biocatalytic approach to the preparation of enantiomerically pure chiral building blocks Chem. Rev. 92 1992 1071 1140
    • (1992) Chem. Rev. , vol.92 , pp. 1071-1140
    • Santoniello, E.1    Ferraloschi, P.2    Grisent, P.3    Monzouchi, A.4
  • 12
    • 0031737276 scopus 로고    scopus 로고
    • Lipase-catalyzed kinetic resolution of the racemic mixtures of 1-aryloxy-3-nitrato and 1-aryloxy-3-azido-2-propanols
    • P. Beata, R. Justyna, and Plenkiewicz Lipase-catalyzed kinetic resolution of the racemic mixtures of 1-aryloxy-3-nitrato and 1-aryloxy-3-azido-2- propanols Synthetic Commun. 28 1998 4355 4364
    • (1998) Synthetic Commun. , vol.28 , pp. 4355-4364
    • Beata, P.1    Justyna, R.2
  • 13
    • 0036211041 scopus 로고    scopus 로고
    • Purification and characterization of lipase from the anaerobic lipolytic bacterium Selenomonas lipolytica
    • A. Behere, A.S. Dighe, S.B. Bhosale, and D.R. Ranade Purification and characterization of lipase from the anaerobic lipolytic bacterium Selenomonas lipolytica J. Microbiol. Biotechnol. 12 2002 142 144
    • (2002) J. Microbiol. Biotechnol. , vol.12 , pp. 142-144
    • Behere, A.1    Dighe, A.S.2    Bhosale, S.B.3    Ranade, D.R.4
  • 14
    • 0031054955 scopus 로고    scopus 로고
    • Process development for the production of the (S)-acid precursor of a novel elastase inhibitor (L-694, 458) through the lipase-catalyzed kinetic resolution of a β-lactam benzyl ester
    • R. Christopher, J.C. Raymond, S.A. Joseph, P. Victor, W.H. Frederick, and G. Randolph Process development for the production of the (S)-acid precursor of a novel elastase inhibitor (L-694, 458) through the lipase-catalyzed kinetic resolution of a β-lactam benzyl ester J. Ferm Bioeng. 83 1997 48 53
    • (1997) J. Ferm Bioeng. , vol.83 , pp. 48-53
    • Christopher, R.1    Raymond, J.C.2    Joseph, S.A.3    Victor, P.4    Frederick, W.H.5    Randolph, G.6
  • 15
    • 20644455034 scopus 로고
    • Resolution of racemic mixtures via lipase catalysis in organic solvents
    • G. Kirchner, M.P. Scollar, and A.M. Klibanov Resolution of racemic mixtures via lipase catalysis in organic solvents J. Am. Chem. Soc. 107 1985 7072 7076
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 7072-7076
    • Kirchner, G.1    Scollar, M.P.2    Klibanov, A.M.3
  • 16
    • 0027999035 scopus 로고
    • Production of optically active 3-phenylglycidic acid ester by the lipase from Serratia marcescens on a hollow-fiber membrane reactor
    • H. Matsumae, M. Furui, T. Shibatani, and T. Tosa Production of optically active 3-phenylglycidic acid ester by the lipase from Serratia marcescens on a hollow-fiber membrane reactor J. Ferment. Bioeng. 78 1994 59 63
    • (1994) J. Ferment. Bioeng. , vol.78 , pp. 59-63
    • Matsumae, H.1    Furui, M.2    Shibatani, T.3    Tosa, T.4
  • 17
    • 0033587799 scopus 로고    scopus 로고
    • Optimizing lipase activity, enantioselectivity, and stability with medium engineering and immobilization for β-blocker synthesis
    • S.C. Mohapatra, and J.T. Hsu Optimizing lipase activity, enantioselectivity, and stability with medium engineering and immobilization for β-blocker synthesis Biotech. Bioeng. 64 1999 213 220
    • (1999) Biotech. Bioeng. , vol.64 , pp. 213-220
    • Mohapatra, S.C.1    Hsu, J.T.2
  • 18
    • 7544221848 scopus 로고    scopus 로고
    • Methods and compositions of (2R, 4S) itraconazole for treating fungal yeast and dermatophyte infections, US Patent No. 5474997 (1995).
    • Gray N.M., Woosley R.L., Methods and compositions of (2R, 4S) itraconazole for treating fungal yeast and dermatophyte infections, US Patent No. 5474997 (1995).
    • Gray, N.M.1    Woosley, R.L.2
  • 19
    • 7544232937 scopus 로고    scopus 로고
    • 2R, 4S, R, S- and 2S, 4R, R, S-hydroxy itraconazole. US Patent No. 5952502 (1999).
    • McCullough J.R., Senanayake C.H., Tanoury G.J., Hohg Y., Koch P., 2R, 4S, R, S- and 2S, 4R, R, S-hydroxy itraconazole. US Patent No. 5952502 (1999).
    • McCullough, J.R.1    Senanayake, C.H.2    Tanoury, G.J.3    Hohg, Y.4    Koch, P.5
  • 21
    • 51249170526 scopus 로고
    • Screening of lipase activities with cultures from the agricultural research services culture collection
    • C.T. Hou, and T.M. Johnston Screening of lipase activities with cultures from the agricultural research services culture collection JAOACS 69 1992 1088 1097
    • (1992) JAOACS , vol.69 , pp. 1088-1097
    • Hou, C.T.1    Johnston, T.M.2
  • 22
    • 20644469267 scopus 로고
    • Quantitative analysis of biochemical kinetic resolutions of enantiomers
    • C.H. Chen, Y. Fujimoto, G. Girdaukas, and C.J. Sih Quantitative analysis of biochemical kinetic resolutions of enantiomers J. Am. Chem. Soc. 104 1982 7294 7299
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 7294-7299
    • Chen, C.H.1    Fujimoto, Y.2    Girdaukas, G.3    Sih, C.J.4
  • 23
    • 0035956401 scopus 로고    scopus 로고
    • Study of the enantioselectivity of the CAL-B-catalyzed transesterification of α-substituted α-propylmethanols and α-substituted benzyl alcohols
    • G.U. Eduardo, F. Rebolledo, and V. Gotor Study of the enantioselectivity of the CAL-B-catalyzed transesterification of α-substituted α-propylmethanols and α-substituted benzyl alcohols Tetrahedron Asymmetry 12 2001 3047 3052
    • (2001) Tetrahedron Asymmetry , vol.12 , pp. 3047-3052
    • Eduardo, G.U.1    Rebolledo, F.2    Gotor, V.3
  • 24
    • 0030271174 scopus 로고    scopus 로고
    • Kinetic resolutions of amine and thiol analogues of secondary alcohols catalyzed by the Candida Antarctica lipase B
    • O. Niklas, C. Orrenius, A. Mattson, T. Norin, and K. Hult Kinetic resolutions of amine and thiol analogues of secondary alcohols catalyzed by the Candida Antarctica lipase B Enzyme Microb. Technol. 19 1996 328 331
    • (1996) Enzyme Microb. Technol. , vol.19 , pp. 328-331
    • Niklas, O.1    Orrenius, C.2    Mattson, A.3    Norin, T.4    Hult, K.5
  • 25
    • 0029128992 scopus 로고
    • Structure of solvent affects enantioselectivity of lipase-catalyzed transesterification
    • N. Kaoru, K. Masamichi, and O. Atsuyoshi Structure of solvent affects enantioselectivity of lipase-catalyzed transesterification Tetrahedron 51 1995 8799 8808
    • (1995) Tetrahedron , vol.51 , pp. 8799-8808
    • Kaoru, N.1    Masamichi, K.2    Atsuyoshi, O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.