-
1
-
-
0000337135
-
Biocatalytic approaches for the synthesis of enantiopure epoxides
-
Archelas A., Furstoss R. Biocatalytic approaches for the synthesis of enantiopure epoxides. Top. Curr. Chem. 200:1999;160-191.
-
(1999)
Top. Curr. Chem.
, vol.200
, pp. 160-191
-
-
Archelas, A.1
Furstoss, R.2
-
2
-
-
37049067047
-
Regio- And enantio-selectivity of the cytosolic epoxide hydrolase-catalyzed hydrolysis of racemic monosubstituted alkyloxiranes
-
Bellucci G., Chiappe C., Marioni F., Benetti M. Regio- and enantio-selectivity of the cytosolic epoxide hydrolase-catalyzed hydrolysis of racemic monosubstituted alkyloxiranes. J. Chem. Soc. Perkin Trans. 1:1991;361-363.
-
(1991)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 361-363
-
-
Bellucci, G.1
Chiappe, C.2
Marioni, F.3
Benetti, M.4
-
3
-
-
0029040624
-
Stereocontrolled hydrolysis of the linoleic acid monoepoxide regioisomers catalyzed by soy-bean epoxide hydrolase
-
Blée E., Schuber F. Stereocontrolled hydrolysis of the linoleic acid monoepoxide regioisomers catalyzed by soy-bean epoxide hydrolase. Eur. J. Biochem. 230:1995;229-234.
-
(1995)
Eur. J. Biochem.
, vol.230
, pp. 229-234
-
-
Blée, E.1
Schuber, F.2
-
5
-
-
0025969930
-
Increased yield of a lysozyme after self-cloning of the gene in Streptomyces coelicolor "müller"
-
Bräu B., Hilgenfeld R., Schlingmann M. et al. Increased yield of a lysozyme after self-cloning of the gene in Streptomyces coelicolor "Müller" Appl. Microbiol. Biotechnol. 34:1991;481-487.
-
(1991)
Appl. Microbiol. Biotechnol.
, vol.34
, pp. 481-487
-
-
Bräu, B.1
Hilgenfeld, R.2
Schlingmann, M.3
-
6
-
-
20644469267
-
Quantitative analyses of biochemical kinetic resolutions of enantiomers
-
Chen C.S., Fujimoto Y., Girdaukas G., Sih C.J. Quantitative analyses 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.S.1
Fujimoto, Y.2
Girdaukas, G.3
Sih, C.J.4
-
8
-
-
0030222084
-
Novel aliphatic epoxide hydrolase activities from dematiaceous fungi
-
Grogan G., Roberts S.M., Willetts A.J. Novel aliphatic epoxide hydrolase activities from dematiaceous fungi. FEMS Microbiol. Lett. 141:1996;239-243.
-
(1996)
FEMS Microbiol. Lett.
, vol.141
, pp. 239-243
-
-
Grogan, G.1
Roberts, S.M.2
Willetts, A.J.3
-
9
-
-
0031558404
-
Biohydrolysis of substituted styrene oxides by Beauveria densa CMC 3240
-
Grogan G., Rippe C., Willetts A. Biohydrolysis of substituted styrene oxides by Beauveria densa CMC 3240. J. Mol. Catal. B Enzym. 3:1997;253-257.
-
(1997)
J. Mol. Catal. B Enzym.
, vol.3
, pp. 253-257
-
-
Grogan, G.1
Rippe, C.2
Willetts, A.3
-
10
-
-
0028356107
-
Rational design of Mn-Salen epoxidation catalysts: Preliminary results
-
Hosoya N., Hatayama A., Irie R., Sasaki H., Katsuki T. Rational design of Mn-Salen epoxidation catalysts: preliminary results. Tetrahedron. 50:1994;4311-4322.
-
(1994)
Tetrahedron
, vol.50
, pp. 4311-4322
-
-
Hosoya, N.1
Hatayama, A.2
Irie, R.3
Sasaki, H.4
Katsuki, T.5
-
11
-
-
0001780886
-
Asymmetric epoxidation of allylic alcohols: The Katsuki-Sharpless epoxidation reaction
-
Katsuki T., Martin V.S. Asymmetric epoxidation of allylic alcohols: the Katsuki-Sharpless epoxidation reaction. Org. React. (NY). 48:1996;1-299.
-
(1996)
Org. React. (NY)
, vol.48
, pp. 1-299
-
-
Katsuki, T.1
Martin, V.S.2
-
12
-
-
0030580210
-
Deracemization of (±)-cis-2,3-epoxyheptane via enantioconvergent biocatalytic hydrolysis using Nocardia EH1-epoxide hydrolase
-
Kroutil W., Mischitz M., Plachota P., Faber K. Deracemization of (±)-cis-2,3-epoxyheptane via enantioconvergent biocatalytic hydrolysis using Nocardia EH1-epoxide hydrolase. Tetrahedron Lett. 37:1996;8379-8382.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 8379-8382
-
-
Kroutil, W.1
Mischitz, M.2
Plachota, P.3
Faber, K.4
-
13
-
-
0032522192
-
Purification and characterization of a highly selective epoxide hydrolase from Nocardia sp. EH1
-
Kroutil W., Genzel Y., Pietzsch M., Syldatk C., Faber K. Purification and characterization of a highly selective epoxide hydrolase from Nocardia sp. EH1. J. Biotechnol. 61:1998;143-150.
-
(1998)
J. Biotechnol.
, vol.61
, pp. 143-150
-
-
Kroutil, W.1
Genzel, Y.2
Pietzsch, M.3
Syldatk, C.4
Faber, K.5
-
14
-
-
0031944878
-
Stabilization of Nocardia EH1 epoxide hydrolase by immobilization
-
Kroutil W., Orru R.V.A., Faber K. Stabilization of Nocardia EH1 epoxide hydrolase by immobilization. Biotechnol. Lett. 20:1998;373-377.
-
(1998)
Biotechnol. Lett.
, vol.20
, pp. 373-377
-
-
Kroutil, W.1
Orru, R.V.A.2
Faber, K.3
-
15
-
-
0031692755
-
Stereo- And regioselective hydroxylation of α-ionone by Streptomyces strains
-
Lutz-Wahl S., Fischer P., Schmidt-Dannert C., Wohlleben W., Hauer B., Schmid R.D. Stereo- and regioselective hydroxylation of α-ionone by Streptomyces strains. Appl. Environ. Microbiol. 64:1998;3878-3881.
-
(1998)
Appl. Environ. Microbiol.
, vol.64
, pp. 3878-3881
-
-
Lutz-Wahl, S.1
Fischer, P.2
Schmidt-Dannert, C.3
Wohlleben, W.4
Hauer, B.5
Schmid, R.D.6
-
16
-
-
0342817475
-
-
1997. Process for enriching R,S-1,2-epoxide in one enantiomer by using microbes to convert one enantiomer to the other or to preferentially open the epoxide ring, US Patent 5 672 504
-
Matsuyama, A., Kobayashi, Y. 1997. Process for enriching R,S-1,2-epoxide in one enantiomer by using microbes to convert one enantiomer to the other or to preferentially open the epoxide ring, US Patent 5 672 504.
-
-
-
Matsuyama, A.1
Kobayashi, Y.2
-
17
-
-
0032054946
-
Characterization of a catabolic epoxide hydrolase from Corynebacterium sp.
-
Misawa E., Chan Kwo Chion C.K.C., Archer I.V. et al. Characterization of a catabolic epoxide hydrolase from Corynebacterium sp. Eur. J. Biochem. 253:1998;173-183.
-
(1998)
Eur. J. Biochem.
, vol.253
, pp. 173-183
-
-
Misawa, E.1
Chan Kwo Chion, C.K.C.2
Archer, I.V.3
-
18
-
-
0002752120
-
Chemo-enzymatic synthesis of (2R,5S)- And (2R,5R)-5-(1-hydroxy-1-methylethyl)-2-methyl-2-vinyl-tetrahydrofuran ('linalool oxide'): preparative application of a highly selective epoxide hydrolase
-
Mischitz, M., Faber, K., 1996. Chemo-enzymatic synthesis of (2R,5S)- and (2R,5R)-5-(1-hydroxy-1-methylethyl)-2-methyl-2-vinyl-tetrahydrofuran ('linalool oxide'): preparative application of a highly selective epoxide hydrolase. Syn. Lett. 978-979.
-
(1996)
Syn. Lett.
, pp. 978-979
-
-
Mischitz, M.1
Faber, K.2
-
19
-
-
0029090931
-
Isolation of a highly enantioselective epoxide hydrolase from Rhodococcus sp. NCIMB11216
-
Mischitz M., Faber K., Willetts A. Isolation of a highly enantioselective epoxide hydrolase from Rhodococcus sp. NCIMB11216. Biotechnol. Lett. 17:1995;893-898.
-
(1995)
Biotechnol. Lett.
, vol.17
, pp. 893-898
-
-
Mischitz, M.1
Faber, K.2
Willetts, A.3
-
21
-
-
0031149795
-
Asymmetric hydrolysis of racemic para-nitrostyrene oxide using an epoxide hydrolase preparation from Aspergillus niger
-
Morisseau C., Nellaiah H., Archelas A., Furstoss R., Baratti J.C. Asymmetric hydrolysis of racemic para-nitrostyrene oxide using an epoxide hydrolase preparation from Aspergillus niger. Enzym. Microb. Technol. 20:1997;446-452.
-
(1997)
Enzym. Microb. Technol.
, vol.20
, pp. 446-452
-
-
Morisseau, C.1
Nellaiah, H.2
Archelas, A.3
Furstoss, R.4
Baratti, J.C.5
-
23
-
-
0030569736
-
Enantioselective hydrolysis of p-nitrostyrene oxide by an epoxide hydrolase preparation from Aspergillus niger
-
Nellaiah H., Morisseau C., Archelas A., Furstoss R., Baratti J.C. Enantioselective hydrolysis of p-nitrostyrene oxide by an epoxide hydrolase preparation from Aspergillus niger. Biotechnol. Bioeng. 49:1996;70-77.
-
(1996)
Biotechnol. Bioeng.
, vol.49
, pp. 70-77
-
-
Nellaiah, H.1
Morisseau, C.2
Archelas, A.3
Furstoss, R.4
Baratti, J.C.5
-
24
-
-
0015849224
-
Mammalian epoxide hydrases: Inducible enzymes catalysing the inactivation of carcinogenic and cytotoxic metabolites derived from aromatic and olefinic compounds
-
Oesch F. Mammalian epoxide hydrases: inducible enzymes catalysing the inactivation of carcinogenic and cytotoxic metabolites derived from aromatic and olefinic compounds. Xenobiotica. 3:1973;305-340.
-
(1973)
Xenobiotica
, vol.3
, pp. 305-340
-
-
Oesch, F.1
-
25
-
-
0019412892
-
Biosynthesis of nanaomycin: Syntheses of nanaomycin E from nanaomycin A and of nanaomycin B from nanaomycin E in a cell-free system
-
Omura S., Minami S., Tanaka H. Biosynthesis of nanaomycin: syntheses of nanaomycin E from nanaomycin A and of nanaomycin B from nanaomycin E in a cell-free system. J. Biochem. 90:1981;291-293.
-
(1981)
J. Biochem.
, vol.90
, pp. 291-293
-
-
Omura, S.1
Minami, S.2
Tanaka, H.3
-
26
-
-
0007753895
-
Microbial alkene epoxidation - merits and limitations
-
Onumonu A.N., Colocoussi A., Mathews C., Woodland M.P., Leak D.J. Microbial alkene epoxidation - merits and limitations. Biocatalysis. 10:1994;211-218.
-
(1994)
Biocatalysis
, vol.10
, pp. 211-218
-
-
Onumonu, A.N.1
Colocoussi, A.2
Mathews, C.3
Woodland, M.P.4
Leak, D.J.5
-
27
-
-
0031562470
-
Deracemization of (±)-22-disubstituted epoxides via enantioconvergent chemoenzymic hydrolysis using Nocardia EH1 epoxide hydrolase and sulfuric acid
-
Orru R.V.A., Kroutil W., Faber K. Deracemization of (±)-22-disubstituted epoxides via enantioconvergent chemoenzymic hydrolysis using Nocardia EH1 epoxide hydrolase and sulfuric acid. Tetrahedron Lett. 38:1997;1753-1754.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 1753-1754
-
-
Orru, R.V.A.1
Kroutil, W.2
Faber, K.3
-
29
-
-
0031690074
-
An efficient large-scale synthesis of (R)-(-)-mevalonolactone using simple biological and chemical catalysts
-
Orru, R.V.A., Osprian, I., Kroutil, W., Faber, K., 1998. An efficient large-scale synthesis of (R)-(-)-mevalonolactone using simple biological and chemical catalysts. Synthesis, 1259-1263.
-
(1998)
Synthesis
, pp. 1259-1263
-
-
Orru, R.V.A.1
Osprian, I.2
Kroutil, W.3
Faber, K.4
-
30
-
-
0031016293
-
Biocatalytic resolution of 2-methyl-2-(aryl)alkyloxiranes using novel bacterial epoxide hydrolases
-
Osprian I., Kroutil W., Mischitz M., Faber K. Biocatalytic resolution of 2-methyl-2-(aryl)alkyloxiranes using novel bacterial epoxide hydrolases. Tetrahedron Asymmetry. 8:1997;65-71.
-
(1997)
Tetrahedron Asymmetry
, vol.8
, pp. 65-71
-
-
Osprian, I.1
Kroutil, W.2
Mischitz, M.3
Faber, K.4
-
31
-
-
0000462782
-
Epoxydes énantiopurs: Obtention par voie chimique ou par voie enzymatique
-
Pedragosa-Moreau S., Archelas A., Furstoss R. Epoxydes énantiopurs: obtention par voie chimique ou par voie enzymatique. Bull. Soc. Chim. Fr. 132:1995;769-800.
-
(1995)
Bull. Soc. Chim. Fr.
, vol.132
, pp. 769-800
-
-
Pedragosa-Moreau, S.1
Archelas, A.2
Furstoss, R.3
-
32
-
-
0029856005
-
Microbiological transformations. 33. Fungal epoxide hydrolases applied to the synthesis of enantiopure para-substituted styrene oxides. A mechanistic approach
-
Pedragosa-Moreau S., Morisseau C., Zylber J., Archelas A., Baratti J., Furstoss R. Microbiological transformations. 33. Fungal epoxide hydrolases applied to the synthesis of enantiopure para-substituted styrene oxides. A mechanistic approach. J. Org. Chem. 61:1996;7402-7407.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 7402-7407
-
-
Pedragosa-Moreau, S.1
Morisseau, C.2
Zylber, J.3
Archelas, A.4
Baratti, J.5
Furstoss, R.6
-
33
-
-
0025954760
-
Opposite facial specificity for two hydroquinone epoxidases: (3-si,4-re)-2,5-dihydroacetanilide epoxidase from Streptomyces LL-C10037 and (3-re,4-si)-2,5-dihydroxyacetanilide epoxidase from Streptomyces MPP3051
-
Shen B., Gould S.J. Opposite facial specificity for two hydroquinone epoxidases: (3-si,4-re)-2,5-dihydroacetanilide epoxidase from Streptomyces LL-C10037 and (3-re,4-si)-2,5-dihydroxyacetanilide epoxidase from Streptomyces MPP3051. Biochemistry. 30:1991;8936-8944.
-
(1991)
Biochemistry
, vol.30
, pp. 8936-8944
-
-
Shen, B.1
Gould, S.J.2
-
34
-
-
0032512591
-
Enantioselectivity of a recombinant epoxide hydrolase from Agrobacterium radiobacter
-
Spelberg J.H.L., Rink R., Kellogg R.M., Janssen D.B. Enantioselectivity of a recombinant epoxide hydrolase from Agrobacterium radiobacter. Tetrahedron Asymmetry. 9:1998;459-466.
-
(1998)
Tetrahedron Asymmetry
, vol.9
, pp. 459-466
-
-
Spelberg, J.H.L.1
Rink, R.2
Kellogg, R.M.3
Janssen, D.B.4
-
36
-
-
0031579475
-
Enantioselective hydrolysis of aryl, alicyclic and aliphatic epoxides by Rhodotorula glutinis
-
Weijers C.A.G.M. Enantioselective hydrolysis of aryl, alicyclic and aliphatic epoxides by Rhodotorula glutinis. Tetrahedron Asymmetry. 8:1997;639-647.
-
(1997)
Tetrahedron Asymmetry
, vol.8
, pp. 639-647
-
-
Weijers, C.A.G.M.1
-
37
-
-
0033545515
-
Epoxide hydrolases from yeast and other sources: Versatile tools in biocatalysis
-
Weijers C.A.G.M., de Bont J.A.M. Epoxide hydrolases from yeast and other sources: versatile tools in biocatalysis. J. Mol. Catal. B Enzym. 6:1999;199-214.
-
(1999)
J. Mol. Catal. B Enzym.
, vol.6
, pp. 199-214
-
-
Weijers, C.A.G.M.1
De Bont, J.A.M.2
-
38
-
-
0033522895
-
A colorimetric assay suitable for screening epoxide hydrolase activity
-
Zocher F., Enzelberger M.M., Bornscheuer U.T., Hauer B., Schmid R.D. A colorimetric assay suitable for screening epoxide hydrolase activity. Anal. Chim. Acta. 391:1999;345-351.
-
(1999)
Anal. Chim. Acta
, vol.391
, pp. 345-351
-
-
Zocher, F.1
Enzelberger, M.M.2
Bornscheuer, U.T.3
Hauer, B.4
Schmid, R.D.5
|