-
1
-
-
84987255198
-
Synthesis of enantiomers of 1,2-heptanediol
-
Barry, J., Kagan, H. B. 1981. Synthesis of enantiomers of 1,2-heptanediol. Synthesis 6: 453-455.
-
(1981)
Synthesis
, vol.6
, pp. 453-455
-
-
Barry, J.1
Kagan, H.B.2
-
2
-
-
0001142793
-
Reaction engineering for enzyme-catalyzed biotransformations
-
K. Drauz and H, Waldmann, VCH, Weinheim, Germany
-
Biselli, M., Kragl, U., Wandrey, C. 1995. Reaction engineering for enzyme-catalyzed biotransformations, pp 89-155. In: K. Drauz and H, Waldmann, Enzyme catalysis in organic synthesis, 1st edition. VCH, Weinheim, Germany.
-
(1995)
Enzyme Catalysis in Organic Synthesis, 1st Edition
, pp. 89-155
-
-
Biselli, M.1
Kragl, U.2
Wandrey, C.3
-
4
-
-
37049074250
-
Enzymatic resolution of 1,2-diols: Comparison between hydrolysis and transesterification reactions
-
Bosetti, A., Bianchi, D., Cest, P., Golini, P., Spezia, S. 1992. Enzymatic resolution of 1,2-diols: comparison between hydrolysis and transesterification reactions, J. Chem. Soc. Perkin Trans. I: 2395-2398.
-
(1992)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 2395-2398
-
-
Bosetti, A.1
Bianchi, D.2
Cest, P.3
Golini, P.4
Spezia, S.5
-
5
-
-
37049094941
-
The mechanism of asymmetric hydrogenation: Chiral bis(diphenylphosphino)-α-phenylalkane complexes in catalytic and structural studies
-
Brown, J. M., Murrer, B. A. 1982. The mechanism of asymmetric hydrogenation: chiral bis(diphenylphosphino)-α-phenylalkane complexes in catalytic and structural studies. J. Chem. Soc. Perkin Trans. II: 489-497.
-
(1982)
J. Chem. Soc. Perkin Trans.
, vol.2
, pp. 489-497
-
-
Brown, J.M.1
Murrer, B.A.2
-
6
-
-
1842437388
-
The synthesis of benzoyl- and naphthoylcarbinol [experimental note]
-
Cebrián, G. R. 1948. The synthesis of benzoyl- and naphthoylcarbinol [experimental note]. Ann. Soc. Espãn [B] 44: 587-592.
-
(1948)
Ann. Soc. Espãn [B]
, vol.44
, pp. 587-592
-
-
Cebrián, G.R.1
-
7
-
-
0345817539
-
Regeneration of nicotinamide cofactors for use in organic synthesis
-
Chenault, H. K., Whitesides, G. M. 1987. Regeneration of nicotinamide cofactors for use in organic synthesis. Appl. Biochem. Biotechnol. 14: 147-197.
-
(1987)
Appl. Biochem. Biotechnol.
, vol.14
, pp. 147-197
-
-
Chenault, H.K.1
Whitesides, G.M.2
-
9
-
-
84985667706
-
Potential of hollow-fibre modules for non-dispersive chemical extraction
-
Daiminger, U., Plucinski, P., Nitsch, W. 1995. Potential of hollow-fibre modules for non-dispersive chemical extraction. Chem.-Ing.-Technol. 67: 217-220.
-
(1995)
Chem.-Ing.-Technol.
, vol.67
, pp. 217-220
-
-
Daiminger, U.1
Plucinski, P.2
Nitsch, W.3
-
11
-
-
37049088202
-
Enzymes in organic synthesis: Oxidoreductions
-
Fang, J.-M., Lin, C-H., Bradshaw, C.-W., Wong, C-W. 1995. Enzymes in organic synthesis: oxidoreductions. J. Chem. Soc. Perkin Trans 1: 967-978.
-
(1995)
J. Chem. Soc. Perkin Trans
, vol.1
, pp. 967-978
-
-
Fang, J.-M.1
Lin, C.-H.2
Bradshaw, C.-W.3
Wong, C.-W.4
-
12
-
-
84949070047
-
High-yield production of optically active 1,2-diols from the corresponding racemates by microbial stereoinversion
-
Hasegawa, J., Ogura, M., Tsuda, S., Maemoto, S., Kutsuki, H., Ohashi T. 1990. High-yield production of optically active 1,2-diols from the corresponding racemates by microbial stereoinversion. Agric. Biol. Chem. 54: 1819-1827.
-
(1990)
Agric. Biol. Chem.
, vol.54
, pp. 1819-1827
-
-
Hasegawa, J.1
Ogura, M.2
Tsuda, S.3
Maemoto, S.4
Kutsuki, H.5
Ohashi, T.6
-
15
-
-
0001585520
-
Gas chromatographic enantiomer separation of chiral alcohols
-
König, W. A., Francke, W., Benecke, I. 1982. Gas chromatographic enantiomer separation of chiral alcohols. J. Chromatogr. 239: 227-231.
-
(1982)
J. Chromatogr.
, vol.239
, pp. 227-231
-
-
König, W.A.1
Francke, W.2
Benecke, I.3
-
16
-
-
8044223226
-
Enzyme engineering aspects of biocatalysis: Cofactor regeneration as example
-
to appear
-
Kragl, U., Kruse, W., Hummel, W., Wandrey, C. 1995. Enzyme engineering aspects of biocatalysis: cofactor regeneration as example. Biotechnol. Bioeng., to appear.
-
(1995)
Biotechnol. Bioeng.
-
-
Kragl, U.1
Kruse, W.2
Hummel, W.3
Wandrey, C.4
-
17
-
-
0026873227
-
Kontinuierliche Reaktions-führung mit löslichen Enzymen
-
Kragl, U., Racki, D.-V., Wandrey, C. 1992. Kontinuierliche Reaktions-führung mit löslichen Enzymen. Chem.-Eng.-Technol. 64:499-509.
-
(1992)
Chem.-Eng.-Technol.
, vol.64
, pp. 499-509
-
-
Kragl, U.1
Racki, D.-V.2
Wandrey, C.3
-
19
-
-
0023620670
-
Continuous enzymatic transformation in an enzyme-membrane reactor with simultaneous NADH regeneration
-
Kula, M.-R., Wandrey, C. 1987. Continuous enzymatic transformation in an enzyme-membrane reactor with simultaneous NADH regeneration. Methods Enzymol. 136: 9-21.
-
(1987)
Methods Enzymol.
, vol.136
, pp. 9-21
-
-
Kula, M.-R.1
Wandrey, C.2
-
20
-
-
0018544778
-
Preparation of optically active poly-β-propiolactones
-
Leborgne, A., Spassky, N., Sigwalt, P. 1979. Preparation of optically active poly-β-propiolactones. Polym. Bull. 1: 825-832.
-
(1979)
Polym. Bull.
, vol.1
, pp. 825-832
-
-
Leborgne, A.1
Spassky, N.2
Sigwalt, P.3
-
21
-
-
0000697019
-
Enzyme-catalyzed organic synthesis: A comparison of strategies for in situ regeneration of NAD from NADH
-
Lee, L. G., Whitesides, G. M. 1985. Enzyme-catalyzed organic synthesis: a comparison of strategies for in situ regeneration of NAD from NADH. J. Am. Chem. Soc. 107: 6999-7008.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 6999-7008
-
-
Lee, L.G.1
Whitesides, G.M.2
-
22
-
-
0001275962
-
Preparation of optically active 1,2-diols and α-hydroxy ketones using glycerol dehydrogenase as catalyst: Limits to enzyme-catalyzed synthesis due to noncompetitive and mixed inhibition to product
-
Lee, L. G., Whitesides, G. M. 1986. Preparation of optically active 1,2-diols and α-hydroxy ketones using glycerol dehydrogenase as catalyst: limits to enzyme-catalyzed synthesis due to noncompetitive and mixed inhibition to product. J. Org. Chem. 51: 25-36.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 25-36
-
-
Lee, L.G.1
Whitesides, G.M.2
-
23
-
-
72849172526
-
The activation of glycerol dehydrogenase from Aerobacter aerogenes by monovalent cations
-
Lin, E. C. C., Magasanik, B. 1960. The activation of glycerol dehydrogenase from Aerobacter aerogenes by monovalent cations. J. Biol. Chem. 235: 1820-1823.
-
(1960)
J. Biol. Chem.
, vol.235
, pp. 1820-1823
-
-
Lin, E.C.C.1
Magasanik, B.2
-
26
-
-
0016159929
-
Purification and kinetic characterization of a monovalent cation-activated glycerol dehydrogenase from Aerobacter aerogenes
-
McGregor, W. G., Phillips, J., Suelter, H. 1974. Purification and kinetic characterization of a monovalent cation-activated glycerol dehydrogenase from Aerobacter aerogenes. J. Biol. Chem. 249: 3132-3139.
-
(1974)
J. Biol. Chem.
, vol.249
, pp. 3132-3139
-
-
McGregor, W.G.1
Phillips, J.2
Suelter, H.3
-
27
-
-
0010325555
-
Preparative methods for chiral synthons using enzymes
-
Spring Innovations Ltd, Stockport, England
-
Ohashi, T. 1990. Preparative methods for chiral synthons using enzymes, pp. 65-71. In: Proceedings of the Chiral 90 Symposium, Spring Innovations Ltd, Stockport, England.
-
(1990)
Proceedings of the Chiral 90 Symposium
, pp. 65-71
-
-
Ohashi, T.1
-
30
-
-
0027459651
-
Kinetic resolution of aliphatic 1,2-diols by a lipase-catalyzed sequential acetylation
-
Theil, F., Weidner, J., Ballschuh, S., Kunath, A., Schick, H. 1993. Kinetic resolution of aliphatic 1,2-diols by a lipase-catalyzed sequential acetylation. Tetrahedron Lett. 34: 305-306.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 305-306
-
-
Theil, F.1
Weidner, J.2
Ballschuh, S.3
Kunath, A.4
Schick, H.5
-
31
-
-
0004081262
-
-
Verlag Chemie, Weinheim, Germany
-
Voet, D., Voet, J. G. 1992. Biochemie. Verlag Chemie, Weinheim, Germany.
-
(1992)
Biochemie
-
-
Voet, D.1
Voet, J.G.2
-
33
-
-
84941889613
-
Continuous enzymatic transformation in an enzyme membrane reactor with simultaneous NAD(H) regeneration
-
Wichmann, R., Wandrey, C., Bückmann, A. F., Kula, M.-R. 1981. Continuous enzymatic transformation in an enzyme membrane reactor with simultaneous NAD(H) regeneration. Biotechnol. Bioeng. 23: 2789-2802.
-
(1981)
Biotechnol. Bioeng.
, vol.23
, pp. 2789-2802
-
-
Wichmann, R.1
Wandrey, C.2
Bückmann, A.F.3
Kula, M.-R.4
|