-
1
-
-
0347474982
-
Recent developments in asymmetric reduction of ketones with biocatalysts
-
Nakamura K, Yamanaka R, Matsuda T, Harada T. Recent developments in asymmetric reduction of ketones with biocatalysts. Tetrahedron: Asym 2003, 14:2659-2681.
-
(2003)
Tetrahedron: Asym
, vol.14
, pp. 2659-2681
-
-
Nakamura, K.1
Yamanaka, R.2
Matsuda, T.3
Harada, T.4
-
2
-
-
0036843758
-
Microbial/enzymatic synthesis of chiral intermediates for pharmaceuticals
-
Patel RN. Microbial/enzymatic synthesis of chiral intermediates for pharmaceuticals. Enzyme Microb Technol 2002, 31:804-826.
-
(2002)
Enzyme Microb Technol
, vol.31
, pp. 804-826
-
-
Patel, R.N.1
-
3
-
-
48149085409
-
Sila-haloperidol, a silicon analogue of the dopamine (D-2) receptor antagonist haloperidol: synthesis, pharmacological properties, and metabolic fate
-
Tacke R, Popp F, Muller B, Theis B, Burschka C, Hamacher A, Kassack MU, Schepmann D, Wunsch B, Jurva U, Wellner E. Sila-haloperidol, a silicon analogue of the dopamine (D-2) receptor antagonist haloperidol: synthesis, pharmacological properties, and metabolic fate. Chem Med Chem 2008, 3:152-164.
-
(2008)
Chem Med Chem
, vol.3
, pp. 152-164
-
-
Tacke, R.1
Popp, F.2
Muller, B.3
Theis, B.4
Burschka, C.5
Hamacher, A.6
Kassack, M.U.7
Schepmann, D.8
Wunsch, B.9
Jurva, U.10
Wellner, E.11
-
4
-
-
0042074583
-
Silicon chemistry as a novel source of chemical diversity in drug design
-
Bains W, Tacke R. Silicon chemistry as a novel source of chemical diversity in drug design. Curr Opin Drug Discovery Devel 2003, 6:526-543.
-
(2003)
Curr Opin Drug Discovery Devel
, vol.6
, pp. 526-543
-
-
Bains, W.1
Tacke, R.2
-
5
-
-
0028898802
-
Effect of MDL 73,745 on acetylcholine and biogenic amine levels in rat cortex
-
10.1016/0014-2999(95)00014-C, 7781701
-
Zhu XD, Giacobini E, Hornsperger JM. Effect of MDL 73,745 on acetylcholine and biogenic amine levels in rat cortex. Eur J Pharmacol 1995, 276:93-99. 10.1016/0014-2999(95)00014-C, 7781701.
-
(1995)
Eur J Pharmacol
, vol.276
, pp. 93-99
-
-
Zhu, X.D.1
Giacobini, E.2
Hornsperger, J.M.3
-
6
-
-
0016739239
-
Changes produced in the male genital organs of rabbits and dogs by 2,6-cis-diphenylhexamethyl-cyclotetrasiloxane (KABI 1774)
-
Nicander L. Changes produced in the male genital organs of rabbits and dogs by 2,6-cis-diphenylhexamethyl-cyclotetrasiloxane (KABI 1774). Acta Pharmacol Toxicol 1975, 36:40-54.
-
(1975)
Acta Pharmacol Toxicol
, vol.36
, pp. 40-54
-
-
Nicander, L.1
-
7
-
-
0033790267
-
Anticancer effect of 4-[3,5-bis(trimethylsilyl)benzamido] benzoic acid (TAC-101) against A549 non-small cell lung cancer cell line is related to its anti-invasive activity
-
Shibata J, Murakami K, Wierzba K, Aoyagi Y, Hashimoto A, Sano M, Toko T, Yamada Y. Anticancer effect of 4-[3,5-bis(trimethylsilyl)benzamido] benzoic acid (TAC-101) against A549 non-small cell lung cancer cell line is related to its anti-invasive activity. Anticancer Res 2000, 20:3169-3176.
-
(2000)
Anticancer Res
, vol.20
, pp. 3169-3176
-
-
Shibata, J.1
Murakami, K.2
Wierzba, K.3
Aoyagi, Y.4
Hashimoto, A.5
Sano, M.6
Toko, T.7
Yamada, Y.8
-
8
-
-
0030249436
-
Synthesis and resolution of 2-(cyclohexyl-4-(2-quinolylmethoxy)phenyl)methoxyiminopropionic acid, leukotriene biosynthesis inhibitors
-
Kolasa T, Gunn DE, Stewart AO, Brooks CDW. Synthesis and resolution of 2-(cyclohexyl-4-(2-quinolylmethoxy)phenyl)methoxyiminopropionic acid, leukotriene biosynthesis inhibitors. Tetrahedron: Asym 1996, 7:729-736.
-
(1996)
Tetrahedron: Asym
, vol.7
, pp. 729-736
-
-
Kolasa, T.1
Gunn, D.E.2
Stewart, A.O.3
Brooks, C.D.W.4
-
9
-
-
0035177201
-
Enantioselective synthesis of both enantiomers of various propargylic alcohols by use of two oxidoreductases
-
Schubert T, Hummel W, Kula MR, Muller M. Enantioselective synthesis of both enantiomers of various propargylic alcohols by use of two oxidoreductases. Eur J Org Chem 2001, 22:4181-4187.
-
(2001)
Eur J Org Chem
, vol.22
, pp. 4181-4187
-
-
Schubert, T.1
Hummel, W.2
Kula, M.R.3
Muller, M.4
-
10
-
-
47549096858
-
Efficient synthesis of enantiopure (S)-4-(trimethylsilyl)-3-butyn-2-ol via asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one with immobilized Candida parapsilosis CCTCC M203011 cells
-
Zhang BB, Lou WY, Zong MH, Wu H. Efficient synthesis of enantiopure (S)-4-(trimethylsilyl)-3-butyn-2-ol via asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one with immobilized Candida parapsilosis CCTCC M203011 cells. J Mol Catal B: Enzym 2008, 54:122-129.
-
(2008)
J Mol Catal B: Enzym
, vol.54
, pp. 122-129
-
-
Zhang, B.B.1
Lou, W.Y.2
Zong, M.H.3
Wu, H.4
-
11
-
-
34249914542
-
Purification, characterization, gene cloning, and expression of a novel alcohol dehydrogenase with anti-prelog stereospecificity from Candida parapsilosis
-
Nie Y, Xu Y, Mu XQ, Wang HY, Yang M, Xiao R. Purification, characterization, gene cloning, and expression of a novel alcohol dehydrogenase with anti-prelog stereospecificity from Candida parapsilosis. Appl Environment Microbiol 2007, 73:3759-3764.
-
(2007)
Appl Environment Microbiol
, vol.73
, pp. 3759-3764
-
-
Nie, Y.1
Xu, Y.2
Mu, X.Q.3
Wang, H.Y.4
Yang, M.5
Xiao, R.6
-
12
-
-
1842558913
-
Highly enantioselective conversion of racemic 1-phenyl-1,2-ethanediol by stereoinversion involving a novel cofactor-dependent oxidoreduction system of Candida parapsilosis CCTCC M203011
-
Nie Y, Xu Y, Mu XQ. Highly enantioselective conversion of racemic 1-phenyl-1,2-ethanediol by stereoinversion involving a novel cofactor-dependent oxidoreduction system of Candida parapsilosis CCTCC M203011. Org Process 2004, 8:246-251.
-
(2004)
Org Process
, vol.8
, pp. 246-251
-
-
Nie, Y.1
Xu, Y.2
Mu, X.Q.3
-
13
-
-
34547137887
-
Biocatalytic ketone reduction - a powerful tool for the production of chiral alcohols - part II: whole-cell reductions
-
10.1007/s00253-007-1005-x, 17486338
-
Goldberg K, Schroer K, Lutz S, Liese A. Biocatalytic ketone reduction - a powerful tool for the production of chiral alcohols - part II: whole-cell reductions. Appl Microbiol Biotechnol 2007, 76:249-255. 10.1007/s00253-007-1005-x, 17486338.
-
(2007)
Appl Microbiol Biotechnol
, vol.76
, pp. 249-255
-
-
Goldberg, K.1
Schroer, K.2
Lutz, S.3
Liese, A.4
-
14
-
-
3142634523
-
Efficient synthesis of optically active organosilyl alcohol via asymmetric reduction of acyl silane with immobilized yeast
-
Lou WY, Zong MH, Zhang YY, Wu H. Efficient synthesis of optically active organosilyl alcohol via asymmetric reduction of acyl silane with immobilized yeast. Enzyme Microb Technol 2004, 35:190-196.
-
(2004)
Enzyme Microb Technol
, vol.35
, pp. 190-196
-
-
Lou, W.Y.1
Zong, M.H.2
Zhang, Y.Y.3
Wu, H.4
-
15
-
-
28944451564
-
Biocatalytic synthesis of ethyl (S)-4-chloro-3-hydroxybutanoate in an aqueous-organic solvent biphasic system using Aureobasidium pullulans CGMCC 1244
-
He JY, Sun ZH, Ruan WQ, Xu Y. Biocatalytic synthesis of ethyl (S)-4-chloro-3-hydroxybutanoate in an aqueous-organic solvent biphasic system using Aureobasidium pullulans CGMCC 1244. Process Biochem 2006, 41:244-249.
-
(2006)
Process Biochem
, vol.41
, pp. 244-249
-
-
He, J.Y.1
Sun, Z.H.2
Ruan, W.Q.3
Xu, Y.4
-
16
-
-
0041981949
-
Whole-cell biocatalysis in organic media
-
Leon R, Fernandes P, Pinheiro HM, Cabral JMS. Whole-cell biocatalysis in organic media. Enzyme Microb Technol 1998, 23:483-500.
-
(1998)
Enzyme Microb Technol
, vol.23
, pp. 483-500
-
-
Leon, R.1
Fernandes, P.2
Pinheiro, H.M.3
Cabral, J.M.S.4
-
17
-
-
34447136294
-
Biocatalysis in ionic liquids
-
10.1021/cr050946x, 17564484
-
van Rantwijk F, Sheldon RA. Biocatalysis in ionic liquids. Chem Rev 2007, 107:2757-2785. 10.1021/cr050946x, 17564484.
-
(2007)
Chem Rev
, vol.107
, pp. 2757-2785
-
-
van Rantwijk, F.1
Sheldon, R.A.2
-
18
-
-
2442698764
-
Enantioselective chemo- and bio-catalysis in ionic liquids
-
Song CE. Enantioselective chemo- and bio-catalysis in ionic liquids. Chem Commun 2004, 9:1033-1043.
-
(2004)
Chem Commun
, vol.9
, pp. 1033-1043
-
-
Song, C.E.1
-
19
-
-
18144362501
-
Ionic liquids: Green solvents for nonaqueous biocatalysis
-
Yang Z, Pan WB. Ionic liquids: Green solvents for nonaqueous biocatalysis. Enzyme Microb Technol 2005, 37:19-28.
-
(2005)
Enzyme Microb Technol
, vol.37
, pp. 19-28
-
-
Yang, Z.1
Pan, W.B.2
-
20
-
-
22544477827
-
Markedly improving lipase-mediated asymmetric ammonolysis of D, L-p-hydroxyphenylglycine methyl ester by using an ionic liquid as the reaction medium
-
Lou WY, Zong MH, Wu H, Xu R, Wang JF. Markedly improving lipase-mediated asymmetric ammonolysis of D, L-p-hydroxyphenylglycine methyl ester by using an ionic liquid as the reaction medium. Green Chem 2005, 7:500-506.
-
(2005)
Green Chem
, vol.7
, pp. 500-506
-
-
Lou, W.Y.1
Zong, M.H.2
Wu, H.3
Xu, R.4
Wang, J.F.5
-
21
-
-
33750368436
-
Efficient kinetic resolution of (R, S)-1-trimethylsilylethanol via lipase-mediated enantioselective acylation in ionic liquids
-
10.1002/chir.20307, 16917836
-
Lou WY, Zong MH. Efficient kinetic resolution of (R, S)-1-trimethylsilylethanol via lipase-mediated enantioselective acylation in ionic liquids. Chirality 2006, 18:814-821. 10.1002/chir.20307, 16917836.
-
(2006)
Chirality
, vol.18
, pp. 814-821
-
-
Lou, W.Y.1
Zong, M.H.2
-
22
-
-
33645452986
-
Use of ionic liquids to improve whole-cell biocatalytic asymmetric reduction of acetyltrimethylsilane for efficient synthesis of enantiopure (S)-1-trimethylsilylethanol
-
Lou WY, Zong MH, Smith TJ. Use of ionic liquids to improve whole-cell biocatalytic asymmetric reduction of acetyltrimethylsilane for efficient synthesis of enantiopure (S)-1-trimethylsilylethanol. Green Chem 2006, 8:147-155.
-
(2006)
Green Chem
, vol.8
, pp. 147-155
-
-
Lou, W.Y.1
Zong, M.H.2
Smith, T.J.3
-
23
-
-
34548526273
-
Asymmetric whole cell biotransformations in biphasic ionic liquid/water-systems by use of recombinant Escherichia coli with intracellular cofactor regeneration
-
Bräutigam S, Bringer-Meyer S, Weuster-Botz D. Asymmetric whole cell biotransformations in biphasic ionic liquid/water-systems by use of recombinant Escherichia coli with intracellular cofactor regeneration. Tetrahedron: Asym 2007, 18:1883-887.
-
(2007)
Tetrahedron: Asym
, vol.18
, pp. 1883-1887
-
-
Bräutigam, S.1
Bringer-Meyer, S.2
Weuster-Botz, D.3
-
24
-
-
33744522590
-
An effective method to use ionic liquids as reaction media for asymmetric reduction by Geotrichum candidum
-
Matsuda T, Yamagishi Y, Koguchi S, Iwai N, Kitazume T. An effective method to use ionic liquids as reaction media for asymmetric reduction by Geotrichum candidum. Tetrahedron Lett 2006, 47:4619-4622.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 4619-4622
-
-
Matsuda, T.1
Yamagishi, Y.2
Koguchi, S.3
Iwai, N.4
Kitazume, T.5
-
25
-
-
56049101391
-
Use of an ionic liquid to improve asymmetric reduction of 4'-methoxyacetophenone catalyzed by immobilized Rhodotorula sp AS2.2241 cells
-
Wang W, Zong MH, Lou WY. Use of an ionic liquid to improve asymmetric reduction of 4'-methoxyacetophenone catalyzed by immobilized Rhodotorula sp AS2.2241 cells. J Mol Catal B: Enzym 2009, 56:70-76.
-
(2009)
J Mol Catal B: Enzym
, vol.56
, pp. 70-76
-
-
Wang, W.1
Zong, M.H.2
Lou, W.Y.3
-
26
-
-
58349085768
-
Microbial reduction of ethyl acetoacetate to ethyl (R)-3-hydroxybutyrate in an ionic liquid containing system
-
He JY, Zhou LM, Wang P, Zu L. Microbial reduction of ethyl acetoacetate to ethyl (R)-3-hydroxybutyrate in an ionic liquid containing system. Process Biochem 2009, 44:316-321.
-
(2009)
Process Biochem
, vol.44
, pp. 316-321
-
-
He, J.Y.1
Zhou, L.M.2
Wang, P.3
Zu, L.4
-
27
-
-
4544250331
-
Efficient whole-cell biotransformation in a biphasic ionic liquid/water system
-
Pfruender H, Amidjojo M, Kragl U, Weuster-Botz D. Efficient whole-cell biotransformation in a biphasic ionic liquid/water system. Angew Chem Int Ed 2004, 43:4529-4531.
-
(2004)
Angew Chem Int Ed
, vol.43
, pp. 4529-4531
-
-
Pfruender, H.1
Amidjojo, M.2
Kragl, U.3
Weuster-Botz, D.4
-
28
-
-
0034691792
-
Room temperature ionic liquids as replacements for organic solvents in multiphase bioprocess operations
-
10.1002/(SICI)1097-0290(20000720)69:2<227::AID-BIT12>3.0.CO;2-0, 10861402
-
Cull SG, Holbrey JD, Vargas MV, Seddon KR, Lye GJ. Room temperature ionic liquids as replacements for organic solvents in multiphase bioprocess operations. Biotechnol Bioeng 2000, 69:227-233. 10.1002/(SICI)1097-0290(20000720)69:2<227::AID-BIT12>3.0.CO;2-0, 10861402.
-
(2000)
Biotechnol Bioeng
, vol.69
, pp. 227-233
-
-
Cull, S.G.1
Holbrey, J.D.2
Vargas, M.V.3
Seddon, K.R.4
Lye, G.J.5
-
29
-
-
33744536417
-
Water immiscible ionic liquids as solvents for whole cell biocatalysis
-
10.1016/j.jbiotec.2005.12.004, 16413078
-
Pfruender H, Jones R, Weuster-Botz D. Water immiscible ionic liquids as solvents for whole cell biocatalysis. J Biotechnol 2006, 124:182-190. 10.1016/j.jbiotec.2005.12.004, 16413078.
-
(2006)
J Biotechnol
, vol.124
, pp. 182-190
-
-
Pfruender, H.1
Jones, R.2
Weuster-Botz, D.3
-
30
-
-
44649095105
-
Using a biphasic ionic liquid/water reaction system to improve oxygenase-catalysed biotransformation with whole cells
-
Cornmell RJ, Winder CL, Schuler S, Goodacre R, Stephens G. Using a biphasic ionic liquid/water reaction system to improve oxygenase-catalysed biotransformation with whole cells. Green Chem 2008, 10:685-691.
-
(2008)
Green Chem
, vol.10
, pp. 685-691
-
-
Cornmell, R.J.1
Winder, C.L.2
Schuler, S.3
Goodacre, R.4
Stephens, G.5
-
31
-
-
36148952478
-
Asymmetric biocatalytic reduction of ketones using hydroxy-functionalised water-miscible ionic liquids as solvents
-
de Gonzalo G, Lavandera I, Durchschein K, Wurm D, Faber K, Kroutil W. Asymmetric biocatalytic reduction of ketones using hydroxy-functionalised water-miscible ionic liquids as solvents. Tetrahedron: Asym 2007, 18:2541-2546.
-
(2007)
Tetrahedron: Asym
, vol.18
, pp. 2541-2546
-
-
de Gonzalo, G.1
Lavandera, I.2
Durchschein, K.3
Wurm, D.4
Faber, K.5
Kroutil, W.6
-
32
-
-
0242275111
-
Preparation and characterization of three room-temperature ionic liquids
-
Zhao H, Malhotra SV, Luo RG. Preparation and characterization of three room-temperature ionic liquids. Phys Chem Liquids 2003, 41:545-557.
-
(2003)
Phys Chem Liquids
, vol.41
, pp. 545-557
-
-
Zhao, H.1
Malhotra, S.V.2
Luo, R.G.3
-
33
-
-
0029117101
-
Biotransformations with Rhizopus arrhizus - Preparation of the enantiomers of 1-phenylethanol and 1-(o-methoxyphenyl, m-methoxyphenyl and p-methoxyphenyl)ethanols
-
Salvi NA, Patil PN, Udupa SR, Banerji A. Biotransformations with Rhizopus arrhizus - Preparation of the enantiomers of 1-phenylethanol and 1-(o-methoxyphenyl, m-methoxyphenyl and p-methoxyphenyl)ethanols. Tetrahedron: Asym 1995, 6:2287-2290.
-
(1995)
Tetrahedron: Asym
, vol.6
, pp. 2287-2290
-
-
Salvi, N.A.1
Patil, P.N.2
Udupa, S.R.3
Banerji, A.4
-
34
-
-
0033890961
-
Organic transformations catalyzed by engineered yeast cells and related systems
-
10.1016/S0958-1669(00)00111-7, 10975455
-
Stewart JD. Organic transformations catalyzed by engineered yeast cells and related systems. Curr Opin Biotechnol 2000, 11:363-368. 10.1016/S0958-1669(00)00111-7, 10975455.
-
(2000)
Curr Opin Biotechnol
, vol.11
, pp. 363-368
-
-
Stewart, J.D.1
-
35
-
-
0037164165
-
Significantly improved esterase activity of Trichosporon brassicae cells for ketoprofen resolution by 2-propanol treatment
-
Shen D, Xu JH, Wu HY, Liu YY. Significantly improved esterase activity of Trichosporon brassicae cells for ketoprofen resolution by 2-propanol treatment. J Mol Catal B: Enzym 2002, 18:219-224.
-
(2002)
J Mol Catal B: Enzym
, vol.18
, pp. 219-224
-
-
Shen, D.1
Xu, J.H.2
Wu, H.Y.3
Liu, Y.Y.4
|