-
1
-
-
0028888771
-
Yeast catalysed reduction of β-keto esters (2): Optimization of the stereospecific reduction by Zygosaccharomyces rouxii
-
Hallinan KO, Crout DHG, Hunt JR, Carter AS, Dalton H, Murrell JC, Holt RA, Crosby J (1995) Yeast catalysed reduction of β-keto esters (2): optimization of the stereospecific reduction by Zygosaccharomyces rouxii. Biocatalysis Biotransform 12: 179-191
-
(1995)
Biocatalysis Biotransform
, vol.12
, pp. 179-191
-
-
Hallinan, K.O.1
Crout, D.H.G.2
Hunt, J.R.3
Carter, A.S.4
Dalton, H.5
Murrell, J.C.6
Holt, R.A.7
Crosby, J.8
-
2
-
-
0025165652
-
Phosphorus-containing inhibitors of HMG-CoA reductase. 1. 4-[2-(Arylethyl)hydroxyphosphinyl]-3-hydroxy-butanoic acids: A new class of cell-selective inhibitors of cholesterol biosynthesis
-
Karanewsky DS, Badia MC, Ciosek CP Jr, Robl JF, Sofia MJ, Simpkins LM, DeLange B, Harrity TW, Biller SA, Gordon EM (1990) Phosphorus-containing inhibitors of HMG-CoA reductase. 1. 4-[2-(Arylethyl)hydroxyphosphinyl]-3-hydroxy-butanoic acids: a new class of cell-selective inhibitors of cholesterol biosynthesis. J Med Chem 33: 2952-2956
-
(1990)
J Med Chem
, vol.33
, pp. 2952-2956
-
-
Karanewsky, D.S.1
Badia, M.C.2
Ciosek C.P., Jr.3
Robl, J.F.4
Sofia, M.J.5
Simpkins, L.M.6
Delange, B.7
Harrity, T.W.8
Biller, S.A.9
Gordon, E.M.10
-
3
-
-
0026772563
-
A novel NADPH-dependent carbonyl reductase of Candida macedoniensis: Purification and characterization
-
Kataoka M, Doi Y, Sim T-S, Shimizu S, Yamada H (1992) A novel NADPH-dependent carbonyl reductase of Candida macedoniensis: purification and characterization. Arch Biochem Biophys 294: 469-474
-
(1992)
Arch Biochem Biophys
, vol.294
, pp. 469-474
-
-
Kataoka, M.1
Doi, Y.2
Sim, T.-S.3
Shimizu, S.4
Yamada, H.5
-
5
-
-
1542694981
-
Synthesis of 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl(BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of α-(acrylamino)acrylic acids
-
Miyashita A, Yasuda A, Takaya H, Toriumi K, Ito T, Souchi T, Noyori R (1980) Synthesis of 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl(BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of α-(acrylamino)acrylic acids. J Am Chem Soc 102: 7932-7934
-
(1980)
J Am Chem Soc
, vol.102
, pp. 7932-7934
-
-
Miyashita, A.1
Yasuda, A.2
Takaya, H.3
Toriumi, K.4
Ito, T.5
Souchi, T.6
Noyori, R.7
-
6
-
-
0026928572
-
Stereoselective reduction of β-keto esters by Geotrichum candidum
-
Patel RN, MCMamee CG, Banerjee A, Howell JM, Robison RS, Szarka LJ (1992) Stereoselective reduction of β-keto esters by Geotrichum candidum. Enzyme Microb Technol 14: 731-738
-
(1992)
Enzyme Microb Technol
, vol.14
, pp. 731-738
-
-
Patel, R.N.1
McMamee, C.G.2
Banerjee, A.3
Howell, J.M.4
Robison, R.S.5
Szarka, L.J.6
-
7
-
-
0027703642
-
A novel NADH-dependent carbonyl reductase with an extremely broad substrate range from Candida parapsilosis: Purification and characterization
-
Peters J, Minuth T, Kula M-R (1993) A novel NADH-dependent carbonyl reductase with an extremely broad substrate range from Candida parapsilosis: purification and characterization. Enzyme Microb Technol 15: 950-958
-
(1993)
Enzyme Microb Technol
, vol.15
, pp. 950-958
-
-
Peters, J.1
Minuth, T.2
Kula, M.-R.3
-
8
-
-
33847087242
-
Enzyme-catalyzed organic synthesis: NADH regeneration by using formate dehydrogenase
-
Shaked Z, Whitesides M (1980) Enzyme-catalyzed organic synthesis: NADH regeneration by using formate dehydrogenase. J Am Chem Soc 102: 7104-7105
-
(1980)
J Am Chem Soc
, vol.102
, pp. 7104-7105
-
-
Shaked, Z.1
Whitesides, M.2
-
9
-
-
33845379674
-
Stereochemical control of yeast reduction. 5. Characterization of the oxidoreductases involved in the reduction of β-keto esters
-
Shieh W-R, Gopalan AS, Sih CJ (1985) Stereochemical control of yeast reduction. 5. Characterization of the oxidoreductases involved in the reduction of β-keto esters. J Am Chem Soc 107: 2993-2994
-
(1985)
J Am Chem Soc
, vol.107
, pp. 2993-2994
-
-
Shieh, W.-R.1
Gopalan, A.S.2
Sih, C.J.3
-
10
-
-
0025697029
-
Stereospecific reduction of 3-keto acid esters by a novel aldehyde reductase of Sporobolomyces salmonicolor in a water-organic solvent two-phasic system
-
Shimizu S, Yamada H (1990) Stereospecific reduction of 3-keto acid esters by a novel aldehyde reductase of Sporobolomyces salmonicolor in a water-organic solvent two-phasic system. Ann NY Acad Sci 613: 628-632
-
(1990)
Ann NY Acad Sci
, vol.613
, pp. 628-632
-
-
Shimizu, S.1
Yamada, H.2
-
11
-
-
0013620538
-
Microbial carbonyl reductases-their diversity and application to the synthesis of optically active alcohols
-
Shimizu S, Yamada H (1991) Microbial carbonyl reductases-their diversity and application to the synthesis of optically active alcohols. Yuki Gousei Kagaku 49: 52-62
-
(1991)
Yuki Gousei Kagaku
, vol.49
, pp. 52-62
-
-
Shimizu, S.1
Yamada, H.2
-
12
-
-
0025281564
-
Stereoselective reduction of ethyl 4-chloro-3-oxobutanoate by a microbial aldehyde reductase in an organic solvent-water diphasic system
-
Shimizu S, Kataoka M, Katoh M, Morikawa T, Miyoshi T, Yamada H (1990) Stereoselective reduction of ethyl 4-chloro-3-oxobutanoate by a microbial aldehyde reductase in an organic solvent-water diphasic system. Appl Environ Microb 56: 2374-2377
-
(1990)
Appl Environ Microb
, vol.56
, pp. 2374-2377
-
-
Shimizu, S.1
Kataoka, M.2
Katoh, M.3
Morikawa, T.4
Miyoshi, T.5
Yamada, H.6
-
13
-
-
0022101149
-
Chiral compounds synthesized by biocatalytic reductions
-
Simon H, Bader J, Gunther H, Neumann S, Thanos J (1985) Chiral compounds synthesized by biocatalytic reductions. Angew Chem Int Ed Engl 24: 539-553
-
(1985)
Angew Chem Int Ed Engl
, vol.24
, pp. 539-553
-
-
Simon, H.1
Bader, J.2
Gunther, H.3
Neumann, S.4
Thanos, J.5
-
14
-
-
0025294272
-
A novel NADPH-dependent aldehyde reductase, catalyzing asymmetric reduction of β-keto esters, from Sporobolomyces salmonicolor: Purification and characterization
-
Yamada H, Shimizu S. Kataoka M, Sakai H, Miyoshi T (1990) A novel NADPH-dependent aldehyde reductase, catalyzing asymmetric reduction of β-keto esters, from Sporobolomyces salmonicolor: purification and characterization. FEMS Microbiol Lett 70: 45-48
-
(1990)
FEMS Microbiol Lett
, vol.70
, pp. 45-48
-
-
Yamada, H.1
Shimizu, S.2
Kataoka, M.3
Sakai, H.4
Miyoshi, T.5
-
15
-
-
0013621771
-
The co-immobilization of NAD and dehydrogenases and its application to bioreactors for synthesis and analysis
-
Yamazaki Y, Maeda H (1982) The co-immobilization of NAD and dehydrogenases and its application to bioreactors for synthesis and analysis. Agric Biol Chem 46: 1571-1581
-
(1982)
Agric Biol Chem
, vol.46
, pp. 1571-1581
-
-
Yamazaki, Y.1
Maeda, H.2
-
16
-
-
0000999905
-
Enzyme-catalyzed organic synthesis: NAD(P)H cofactor regeneration by using glucose 6-phosphate and the glucose-6-phosphate dehydrogenase from Leuconostoc mesenteroides
-
Wong C-H, Whitesides GM (1981) Enzyme-catalyzed organic synthesis: NAD(P)H cofactor regeneration by using glucose 6-phosphate and the glucose-6-phosphate dehydrogenase from Leuconostoc mesenteroides. J Am Chem Soc 103: 4890-4899
-
(1981)
J Am Chem Soc
, vol.103
, pp. 4890-4899
-
-
Wong, C.-H.1
Whitesides, G.M.2
-
17
-
-
0022076889
-
Enzymatic vs. fermentative synthesis: Thermostable glucose dehydrogenase catalyzed regeneration of NAD(P)H for use in enzymatic synthesis
-
Wong C-H, Drueckhammer DG, Sweers HM (1985) Enzymatic vs. fermentative synthesis: thermostable glucose dehydrogenase catalyzed regeneration of NAD(P)H for use in enzymatic synthesis. J Am Chem Soc. 107: 4028-4031
-
(1985)
J Am Chem Soc
, vol.107
, pp. 4028-4031
-
-
Wong, C.-H.1
Drueckhammer, D.G.2
Sweers, H.M.3
-
18
-
-
33845552079
-
Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine
-
Zhou B, Gopalan AS, VanMiddlesworth F, Shieh W-R, Sih CJ (1983) Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine. J Am Chem Soc 105: 5925-5926
-
(1983)
J Am Chem Soc
, vol.105
, pp. 5925-5926
-
-
Zhou, B.1
Gopalan, A.S.2
Van Middlesworth, F.3
Shieh, W.-R.4
Sih, C.J.5
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