-
1
-
-
0642282213
-
Biotransformations of non-natural compounds: State of the art and future development
-
K. Faber Biotransformations of non-natural compounds: state of the art and future development Pure Appl Chem 69 1997 1613 1632
-
(1997)
Pure Appl Chem
, vol.69
, pp. 1613-1632
-
-
Faber, K.1
-
2
-
-
0036900263
-
The production of fine chemicals by biotransformations
-
Straathof AJJ, S. Panke, and A. Schmid The production of fine chemicals by biotransformations Curr Opin Biotechnol 13 2002 548 556
-
(2002)
Curr Opin Biotechnol
, vol.13
, pp. 548-556
-
-
Ajj, S.1
Panke, S.2
Schmid, A.3
-
3
-
-
10044248344
-
Reaction specificity of enzymes: Catalytic promiscuity in biocatalysis: Using old enzymes to form new bonds and follow new pathways
-
U.T. Bornscheuer, and R.J. Kazlauskas Reaction specificity of enzymes: catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways Angew Chem Int Ed Engl 43 2004 6032 6040
-
(2004)
Angew Chem Int Ed Engl
, vol.43
, pp. 6032-6040
-
-
Bornscheuer, U.T.1
Kazlauskas, R.J.2
-
4
-
-
16244379809
-
Enhancing catalytic promiscuity for biocatalysis
-
in press.
-
Kazlauskas RJ: Enhancing catalytic promiscuity for biocatalysis. Curr Opin Chem Biol 2005, 9:in press.
-
(2005)
Curr Opin Chem Biol
, vol.9
-
-
Kazlauskas, R.J.1
-
5
-
-
0037021012
-
Enantioselective stereoinversion in the kinetic resolution of rac-sec-alkyl sulfates via hydrolysis using alkylsulfatase from Rhodococcus ruber DSM 44541 furnishes homochiral products
-
M. Pogorevc, W. Kroutil, S.M. Wallner, and K. Faber Enantioselective stereoinversion in the kinetic resolution of rac-sec-alkyl sulfates via hydrolysis using alkylsulfatase from Rhodococcus ruber DSM 44541 furnishes homochiral products Angew Chem Int Ed Engl 41 2002 4052 4054 The first application of a stereoselective and enantioselective alkylsulfatase in biocatalysis yields a homochiral product mixture of sec-alcohol and sec-alkyl sulfate ester from racemic starting material.
-
(2002)
Angew Chem Int Ed Engl
, vol.41
, pp. 4052-4054
-
-
Pogorevc, M.1
Kroutil, W.2
Wallner, S.M.3
Faber, K.4
-
6
-
-
0035802951
-
Non-sequential processes for the transformation of a racemate into a single stereoisomeric product: Proposal for stereochemical classification
-
K. Faber Non-sequential processes for the transformation of a racemate into a single stereoisomeric product: proposal for stereochemical classification Chemistry 7 2001 5004 5010
-
(2001)
Chemistry
, vol.7
, pp. 5004-5010
-
-
Faber, K.1
-
7
-
-
0037135406
-
Selectivity-enhancement in enantioselective hydrolysis of sec-alkyl sulfates by an alkylsulfatase from Rhodococcus ruber DSM 4454
-
M. Pogorevc, U.T. Strauss, T. Riermeier, and K. Faber Selectivity-enhancement in enantioselective hydrolysis of sec-alkyl sulfates by an alkylsulfatase from Rhodococcus ruber DSM 4454 Tetrahedron Asymmetry 13 2002 1443 1447
-
(2002)
Tetrahedron Asymmetry
, vol.13
, pp. 1443-1447
-
-
Pogorevc, M.1
Strauss, U.T.2
Riermeier, T.3
Faber, K.4
-
8
-
-
12344276523
-
Highly enantioselective sec-alkyl sulfatase activity of Sulfolobus acidocaldarius DSM 639
-
S.R. Wallner, B.M. Nestl, and K. Faber Highly enantioselective sec-alkyl sulfatase activity of Sulfolobus acidocaldarius DSM 639 Org Lett 6 2004 5009 5010
-
(2004)
Org Lett
, vol.6
, pp. 5009-5010
-
-
Wallner, S.R.1
Nestl, B.M.2
Faber, K.3
-
9
-
-
0037054398
-
Exploration of the biocatalytic potential of a halohydrin dehalogenase using chromogenic substrates
-
J.H. Lutje Spelberg, L. Tang, M. van Gelder, R.M. Kellogg, and D.B. Janssen Exploration of the biocatalytic potential of a halohydrin dehalogenase using chromogenic substrates Tetrahedron Asymmetry 13 2002 1083 1089 Biocatalytic nucleophilic opening of epoxides using a variety of non-natural nucleophiles.
-
(2002)
Tetrahedron Asymmetry
, vol.13
, pp. 1083-1089
-
-
Lutje Spelberg, J.H.1
Tang, L.2
Van Gelder, M.3
Kellogg, R.M.4
Janssen, D.B.5
-
10
-
-
0042367657
-
Highly enantioselective and regioselective biocatalytic azidolysis of aromatic epoxides
-
J.H. Lutje Spelberg, J.E.T. van Hyckama Vlieg, L. Tang, D.B. Janssen, and R.M. Kellogg Highly enantioselective and regioselective biocatalytic azidolysis of aromatic epoxides Org Lett 3 2001 41 43
-
(2001)
Org Lett
, vol.3
, pp. 41-43
-
-
Lutje Spelberg, J.H.1
Van Hyckama Vlieg, J.E.T.2
Tang, L.3
Janssen, D.B.4
Kellogg, R.M.5
-
11
-
-
0042628455
-
Thiamin-diphosphate-dependent enzymes: New aspects of asymmetric C-C bond formation
-
M. Pohl, B. Lingen, and M. Müller Thiamin-diphosphate-dependent enzymes: new aspects of asymmetric C-C bond formation Chemistry 8 2002 5289 5295 Excellent overview on lyase-catalyzed acyloin reactions, featuring benzaldehyde lyase and benzoylformate decarboxylase.
-
(2002)
Chemistry
, vol.8
, pp. 5289-5295
-
-
Pohl, M.1
Lingen, B.2
Müller, M.3
-
12
-
-
0037120881
-
Development of a donor-acceptor concept for enzymatic cross-coupling reactions of aldehydes: The first asymmetric cross-benzoin condensation
-
P. Dünkelmann, D. Kolter-Jung, A. Nitsche, A.S. Demit, P. Siegert, B. Lingen, M. Baumann, M. Pohl, and M. Müller Development of a donor-acceptor concept for enzymatic cross-coupling reactions of aldehydes: the first asymmetric cross-benzoin condensation J Am Chem Soc 124 2002 12084 12085 The first asymmetric enzymatic cross-benzoin reaction catalyzed by benzaldehyde lyase or benzoylformate decarboxylase.
-
(2002)
J Am Chem Soc
, vol.124
, pp. 12084-12085
-
-
Dünkelmann, P.1
Kolter-Jung, D.2
Nitsche, A.3
Demit, A.S.4
Siegert, P.5
Lingen, B.6
Baumann, M.7
Pohl, M.8
Müller, M.9
-
13
-
-
1842578074
-
Industrial methods for the production of optically active intermediates
-
M. Breuer, K. Ditrich, T. Habicher, B. Hauer, M. Kesseler, R. Stürmer, and T. Zelinski Industrial methods for the production of optically active intermediates Angew Chem Int Ed Engl 43 2004 788 824
-
(2004)
Angew Chem Int Ed Engl
, vol.43
, pp. 788-824
-
-
Breuer, M.1
Ditrich, K.2
Habicher, T.3
Hauer, B.4
Kesseler, M.5
Stürmer, R.6
Zelinski, T.7
-
14
-
-
0037385630
-
Semisynthetic production of unnatural L-α-amino acids by metabolic engineering of cysteine-biosynthetic pathway
-
Maier THP Semisynthetic production of unnatural L-α-amino acids by metabolic engineering of cysteine-biosynthetic pathway Nat Biotechnol 21 2003 422 427 Elegant and innovative approach of combining re-engineering of a biosynthetic pathway with exploiting the broad spectrum of O-acetylserine sulfhydrylase.
-
(2003)
Nat Biotechnol
, vol.21
, pp. 422-427
-
-
Thp, M.1
-
15
-
-
0035433593
-
Comparison of the ω-transaminases from different microorganisms and application to production of chiral amines
-
J.-S. Shin, and B.-G. Kim Comparison of the ω-transaminases from different microorganisms and application to production of chiral amines Biosci Biotechnol Biochem 65 2001 1782 1788
-
(2001)
Biosci Biotechnol Biochem
, vol.65
, pp. 1782-1788
-
-
Shin, J.-S.1
Kim, B.-G.2
-
16
-
-
0037012917
-
Exploring the active site of amine:pyruvate aminotransferase on the basis of substrate structure-reactivity relationship: How the enzyme controls substrate specificity and stereoselectivity
-
J.-S. Shin, and B.-G. Kim Exploring the active site of amine:pyruvate aminotransferase on the basis of substrate structure-reactivity relationship: how the enzyme controls substrate specificity and stereoselectivity J Org Chem 67 2002 2848 2853
-
(2002)
J Org Chem
, vol.67
, pp. 2848-2853
-
-
Shin, J.-S.1
Kim, B.-G.2
-
17
-
-
0345393284
-
Microbial synthesis of (R)- and (S)-3,4-dimethoxyamphetamines through stereoselective transamination
-
A. Iwasaki, Y. Yamada, Y. Ikenaka, and J. Hasegawa Microbial synthesis of (R)- and (S)-3,4-dimethoxyamphetamines through stereoselective transamination Biotechnol Lett 25 2003 1843 1846
-
(2003)
Biotechnol Lett
, vol.25
, pp. 1843-1846
-
-
Iwasaki, A.1
Yamada, Y.2
Ikenaka, Y.3
Hasegawa, J.4
-
18
-
-
0035931377
-
One-pot chemo-enzymatic enantiomerisation of racemates
-
K. Soda, T. Oikawa, and K. Yokoigawa One-pot chemo-enzymatic enantiomerisation of racemates J Mol Catal, B Enzym 11 2001 149 153
-
(2001)
J Mol Catal, B Enzym
, vol.11
, pp. 149-153
-
-
Soda, K.1
Oikawa, T.2
Yokoigawa, K.3
-
19
-
-
0037148008
-
Amine boranes: Effective reducing agents for the deracemisation of DL-amino acids using L-amino acid oxidase from Proteus myxofaciens
-
F.-R. Alexandre, D.P. Pantaleone, P.P. Taylor, I.G. Fotheringham, D.J. Ager, and N.J. Turner Amine boranes: effective reducing agents for the deracemisation of DL-amino acids using L-amino acid oxidase from Proteus myxofaciens Tetrahedron Lett 43 2002 707 710
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 707-710
-
-
Alexandre, F.-R.1
Pantaleone, D.P.2
Taylor, P.P.3
Fotheringham, I.G.4
Ager, D.J.5
Turner, N.J.6
-
20
-
-
1842473615
-
Enzyme catalyzed deracemization and dynamic kinetic resolution reactions
-
N.J. Turner Enzyme catalyzed deracemization and dynamic kinetic resolution reactions Curr Opin Chem Biol 8 2004 114 119
-
(2004)
Curr Opin Chem Biol
, vol.8
, pp. 114-119
-
-
Turner, N.J.1
-
21
-
-
0032555561
-
Deracemisation of compounds possessing a sec-alcohol or -amino group through a cyclic oxidation-reduction sequence: A kinetic treatment
-
W. Kroutil, and K. Faber Deracemisation of compounds possessing a sec-alcohol or -amino group through a cyclic oxidation-reduction sequence: a kinetic treatment Tetrahedron Asymmetry 9 1998 2901 2913
-
(1998)
Tetrahedron Asymmetry
, vol.9
, pp. 2901-2913
-
-
Kroutil, W.1
Faber, K.2
-
22
-
-
0037008967
-
Deracemization of α-methylbenzylamine using an enzyme obtained by in vitro evolution
-
M. Alexeeva, A. Enright, M.J. Dawson, M. Mahmoudian, and N.J. Turner Deracemization of α-methylbenzylamine using an enzyme obtained by in vitro evolution Angew Chem Int Ed Engl 41 2002 3177 3180
-
(2002)
Angew Chem Int Ed Engl
, vol.41
, pp. 3177-3180
-
-
Alexeeva, M.1
Enright, A.2
Dawson, M.J.3
Mahmoudian, M.4
Turner, N.J.5
-
23
-
-
0142214752
-
Directed evolution of an amine oxidase possessing both broad substrate specificity and high enantioselectivity
-
R. Carr, M. Alexeeva, A. Enright, T.S.C. Eve, M.J. Dawson, and N.J. Turner Directed evolution of an amine oxidase possessing both broad substrate specificity and high enantioselectivity Angew Chem Int Ed Engl 42 2003 4807 4810 Expanding the substrate spectrum of an enantioselective amine oxidase so that the enzyme can be used for deracemisation of a broad spectrum of amines.
-
(2003)
Angew Chem Int Ed Engl
, vol.42
, pp. 4807-4810
-
-
Carr, R.1
Alexeeva, M.2
Enright, A.3
Eve, T.S.C.4
Dawson, M.J.5
Turner, N.J.6
-
24
-
-
0346780250
-
Directed evolution of enzymes: New biocatalysts for asymmetric synthesis
-
M. Alexeeva, R. Carr, and N.J. Turner Directed evolution of enzymes: new biocatalysts for asymmetric synthesis Org Biomol Chem 1 2003 4133 4137
-
(2003)
Org Biomol Chem
, vol.1
, pp. 4133-4137
-
-
Alexeeva, M.1
Carr, R.2
Turner, N.J.3
-
25
-
-
0032611028
-
Stereoinversions using microbial redox-reactions
-
A.J. Carnell Stereoinversions using microbial redox-reactions Adv Biochem Eng Biotechnol 63 1999 57 72
-
(1999)
Adv Biochem Eng Biotechnol
, vol.63
, pp. 57-72
-
-
Carnell, A.J.1
-
26
-
-
0037034332
-
Microbial deracemization of α-substituted carboxylic acids
-
D. Kato, S. Mitsuda, and H. Ohta Microbial deracemization of α-substituted carboxylic acids Org Lett 4 2002 371 373
-
(2002)
Org Lett
, vol.4
, pp. 371-373
-
-
Kato, D.1
Mitsuda, S.2
Ohta, H.3
-
27
-
-
0141677961
-
Microbial deracemization of α-substituted carboxylic acids: Substrate specificity and mechanistic investigation
-
D. Kato, S. Mitsuda, and H. Ohta Microbial deracemization of α-substituted carboxylic acids: substrate specificity and mechanistic investigation J Org Chem 68 2003 7234 7242 Deracemization of α-aryl- and α-aryloxy-propanoic acids by whole Nocardia cells was shown to proceed via the corresponding CoA intermediate involving a 2-arylpropionyl-CoA epimerase.
-
(2003)
J Org Chem
, vol.68
, pp. 7234-7242
-
-
Kato, D.1
Mitsuda, S.2
Ohta, H.3
-
28
-
-
4644299277
-
Microbial deracemization of α-substituted carboxylic acids: Control of the reaction path
-
D. Kato, K. Miyamaoto, and H. Ohta Microbial deracemization of α-substituted carboxylic acids: control of the reaction path Tetrahedron Asymmetry 15 2004 2965 2973
-
(2004)
Tetrahedron Asymmetry
, vol.15
, pp. 2965-2973
-
-
Kato, D.1
Miyamaoto, K.2
Ohta, H.3
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