-
1
-
-
0026437190
-
FDA's statement for the development of new stereoisomeric drugs
-
Food & Drug Administration
-
Food & Drug Administration: FDA's statement for the development of new stereoisomeric drugs. Chirality 1992;4:338-40
-
(1992)
Chirality
, vol.4
, pp. 338-340
-
-
-
3
-
-
16244379809
-
Enhancing catalytic promiscuity for biocatalysis
-
Kazlauskas RJ. Enhancing catalytic promiscuity for biocatalysis. Curr Opin Chem Biol 2005;9(2):195-201
-
(2005)
Curr Opin Chem Biol
, vol.9
, Issue.2
, pp. 195-201
-
-
Kazlauskas, R.J.1
-
5
-
-
0842325300
-
Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution
-
Reetz MT, Torre C, Eipper A, et al. Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution. Org Lett 2004;6(2):177-80
-
(2004)
Org Lett
, vol.6
, Issue.2
, pp. 177-180
-
-
Reetz, M.T.1
Torre, C.2
Eipper, A.3
-
6
-
-
32544436092
-
Preparation of human metabolites of propranolol using laboratory-evolved bacterial cytochromes P450
-
Otey CR, Bandara G, Lalonde J, et al. Preparation of human metabolites of propranolol using laboratory-evolved bacterial cytochromes P450. Biotech Bioeng 2006;93(3):494-9
-
(2006)
Biotech Bioeng
, vol.93
, Issue.3
, pp. 494-499
-
-
Otey, C.R.1
Bandara, G.2
Lalonde, J.3
-
7
-
-
84967138685
-
Enzyme evolution for chemical process applications
-
Patel RN, editor, CRC Press, FL
-
Huisman GW, Lalonde JJ. Enzyme evolution for chemical process applications. Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 717-42
-
(2007)
Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 717-742
-
-
Huisman, G.W.1
Lalonde, J.J.2
-
8
-
-
0036669389
-
Towards novel processes for the fine-chemical and pharmaceutical industries
-
Huisman GW, Gray D. Towards novel processes for the fine-chemical and pharmaceutical industries. Curr Opin Biotechnol 2002; 13(4):352-8
-
(2002)
Curr Opin Biotechnol
, vol.13
, Issue.4
, pp. 352-358
-
-
Huisman, G.W.1
Gray, D.2
-
9
-
-
0038433222
-
Towards large-scale synthetic applications of Baeyer-Villiger monooxygenases
-
Alphand V, Carrea G, Wohlgemuth R, et al. Towards large-scale synthetic applications of Baeyer-Villiger monooxygenases. Trends Biotechnol 2003;21(7):318-23
-
(2003)
Trends Biotechnol
, vol.21
, Issue.7
, pp. 318-323
-
-
Alphand, V.1
Carrea, G.2
Wohlgemuth, R.3
-
11
-
-
33745762337
-
Biocatalysis: Synthesis of chiral intermediates for pharmaceuticals
-
Patel RN. Biocatalysis: synthesis of chiral intermediates for pharmaceuticals. Curr Org Chem 2006;10(11):1289-321
-
(2006)
Curr Org Chem
, vol.10
, Issue.11
, pp. 1289-1321
-
-
Patel, R.N.1
-
12
-
-
39649097521
-
-
Patel RN, editor, CRC Press, FL
-
Simeo Y, Kroutil W, Faber K. Biocatalytic deracemization: dynamic resolution, stereoinversion, enantioconvergent processes, and cyclic deracemization. Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 27-51
-
(2007)
Biocatalytic deracemization: Dynamic resolution, stereoinversion, enantioconvergent processes, and cyclic deracemization. Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 27-51
-
-
Simeo, Y.1
Kroutil, W.2
Faber, K.3
-
13
-
-
84896837460
-
Towards catalytic cascade reactions: Asymmetric synthesis using combined chemo-enzymatic catalysts
-
Simons C, Hanefeld U, Arends IWCE, et al. Towards catalytic cascade reactions: asymmetric synthesis using combined chemo-enzymatic catalysts. Top Catalysis 2006;40(1-4):35-44
-
(2006)
Top Catalysis
, vol.40
, Issue.1-4
, pp. 35-44
-
-
Simons, C.1
Hanefeld, U.2
Arends, I.W.C.E.3
-
14
-
-
1842473615
-
Enzyme catalyzed deracemization and dynamic kinetic resolution reactions
-
Turner NJ. Enzyme catalyzed deracemization and dynamic kinetic resolution reactions. Curr Opin Chem Biol 2004;8(2):114-9
-
(2004)
Curr Opin Chem Biol
, vol.8
, Issue.2
, pp. 114-119
-
-
Turner, N.J.1
-
15
-
-
16244376779
-
Biocatalysis and biotransformation new technologies, enzymes and challenges
-
Robertson DE, Bornscheuer UT. Biocatalysis and biotransformation new technologies, enzymes and challenges. Curr Opin Chem Biol 2005; 9(2):164-5
-
(2005)
Curr Opin Chem Biol
, vol.9
, Issue.2
, pp. 164-165
-
-
Robertson, D.E.1
Bornscheuer, U.T.2
-
17
-
-
84886071182
-
Green chemical manufacturing with biocatalysis
-
Stewart JD. Green chemical manufacturing with biocatalysis. Environ Catalysis 2005;649-65
-
(2005)
Environ Catalysis
, pp. 649-665
-
-
Stewart, J.D.1
-
18
-
-
84887074117
-
Biotechnological applications of aldolases
-
Patel RN, editor, CRC Press, FL
-
Fessner W-D, Jennewein S. Biotechnological applications of aldolases. Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 363-400
-
(2007)
Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 363-400
-
-
Fessner, W.-D.1
Jennewein, S.2
-
19
-
-
33645677539
-
-
Boyd DR, Bugg TDH. Arene cis-dihydrodiol formation: from biology to application. Org Biomol Chem 2006;4(2):181-92
-
Boyd DR, Bugg TDH. Arene cis-dihydrodiol formation: from biology to application. Org Biomol Chem 2006;4(2):181-92
-
-
-
-
20
-
-
33846197938
-
Biocatalysis for pharmaceutical intermediates: The future is now
-
Pollard DJ, Woodley JM. Biocatalysis for pharmaceutical intermediates: The future is now. Trends Biotechnol 2007;25(2):66-73
-
(2007)
Trends Biotechnol
, vol.25
, Issue.2
, pp. 66-73
-
-
Pollard, D.J.1
Woodley, J.M.2
-
21
-
-
39649112971
-
Industrial processes using lyases for C-C, C-N, and C-C bond formation
-
Patel RN, editor, CRC Press, FL
-
Pohl M, Liese A. Industrial processes using lyases for C-C, C-N, and C-C bond formation. In: Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2006. p. 661-76
-
(2006)
Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 661-676
-
-
Pohl, M.1
Liese, A.2
-
22
-
-
0000532201
-
-
Biocatalysis, Patel RN, editor, Marcel Dekker, NY
-
Effenberger F. Hydroxynitrile lyases in stereoselective synthesis in Stereoselective Biocatalysis, Patel RN, editor, Marcel Dekker, NY. 2000. p. 321-42
-
(2000)
Hydroxynitrile lyases in stereoselective synthesis in Stereoselective
, pp. 321-342
-
-
Effenberger, F.1
-
23
-
-
39649095959
-
-
Biocatalysis. Bommarius AS, Riebel BR, editors, Wiley-VCH. 2004
-
Biocatalysis. Bommarius AS, Riebel BR, editors, Wiley-VCH. 2004
-
-
-
-
24
-
-
39649088340
-
-
Biotransformations in Organic Chemistry. Faber K, editor, Springer. 2005
-
Biotransformations in Organic Chemistry. Faber K, editor, Springer. 2005
-
-
-
-
26
-
-
84889331179
-
-
Industrial Biotransformations. Liese A, Seelbach K, Wandrey C, editors, Wiley-VCH. 2006
-
Industrial Biotransformations. Liese A, Seelbach K, Wandrey C, editors, Wiley-VCH. 2006
-
-
-
-
27
-
-
39649097737
-
-
Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007
-
Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007
-
-
-
-
28
-
-
39649100300
-
Continuous enzymic transformation of water-soluble α-keto carboxylic acids into the corresponding amino acids. Eur
-
Pat Appl, 14pp
-
Wandrey C, Wichmann R, Leuchtenberger W, et al. Continuous enzymic transformation of water-soluble α-keto carboxylic acids into the corresponding amino acids. Eur Pat Appl 1981. 14pp
-
(1981)
-
-
Wandrey, C.1
Wichmann, R.2
Leuchtenberger, W.3
-
29
-
-
0028587754
-
The biochemistry and enzymology of amino acid dehydrogenases
-
Brunhuber NM, Blanchard JS. The biochemistry and enzymology of amino acid dehydrogenases. Crit Rev Biochem Mol Biol 1994;29(6):415-67
-
(1994)
Crit Rev Biochem Mol Biol
, vol.29
, Issue.6
, pp. 415-467
-
-
Brunhuber, N.M.1
Blanchard, J.S.2
-
31
-
-
0025024177
-
Synthesis of L-β-hydroxyvaline from α-keto-βhydroxyisovalerate using leucine dehydrogenase from Bacillus species
-
Hanson RL, Singh J, Kissick TP, et al. Synthesis of L-β-hydroxyvaline from α-keto-βhydroxyisovalerate using leucine dehydrogenase from Bacillus species. Bioorg Chem 1990; 18(2):116-30
-
(1990)
Bioorg Chem
, vol.18
, Issue.2
, pp. 116-130
-
-
Hanson, R.L.1
Singh, J.2
Kissick, T.P.3
-
32
-
-
17644438887
-
Dual metalloprotease inhibitors: Mercaptoacetyl-based fused heterocyclic dipeptide mimetics as inhibitors of angiotensin-converting enzyme and neutral endopeptidase
-
Robl J, Sun C, Stevenson J. Dual metalloprotease inhibitors: mercaptoacetyl-based fused heterocyclic dipeptide mimetics as inhibitors of angiotensin-converting enzyme and neutral endopeptidase. J Med Chem 1997;40:1570-7
-
(1997)
J Med Chem
, vol.40
, pp. 1570-1577
-
-
Robl, J.1
Sun, C.2
Stevenson, J.3
-
34
-
-
0035025463
-
Enzymatic synthesis of chiral intermediates for omapatrilat, an antihypertensive drug
-
Patel R. Enzymatic synthesis of chiral intermediates for omapatrilat, an antihypertensive drug. Biomol Eng 2001;17:167-82
-
(2001)
Biomol Eng
, vol.17
, pp. 167-182
-
-
Patel, R.1
-
35
-
-
0033995512
-
Synthesis of allylsine ethylene acetal using phenylalanine dehydrogenase from Thermoactinomyces intermedius
-
Hanson RL, Howell J, LaPorte T, et al. Synthesis of allylsine ethylene acetal using phenylalanine dehydrogenase from Thermoactinomyces intermedius. Enz Microb Technol 2000;26:348-58
-
(2000)
Enz Microb Technol
, vol.26
, pp. 348-358
-
-
Hanson, R.L.1
Howell, J.2
LaPorte, T.3
-
36
-
-
0017252385
-
Purification and properties of formaldehyde dehydrogenase and formate dehydrogenase from Candida boidinii
-
Schütte H, Flossdorf J, Sahm H, et al. Purification and properties of formaldehyde dehydrogenase and formate dehydrogenase from Candida boidinii. Eur J Biochem 1976;62:151-60
-
(1976)
Eur J Biochem
, vol.62
, pp. 151-160
-
-
Schütte, H.1
Flossdorf, J.2
Sahm, H.3
-
37
-
-
0020144640
-
NAD-linked formate dehydrogenase from methanol-grown Pichia pastoris NRRL-Y-7556
-
Hou CT, Patel RN, Laskin AI, et al. NAD-linked formate dehydrogenase from methanol-grown Pichia pastoris NRRL-Y-7556. Arch Biochem Biophys 1982;216(1):296-305
-
(1982)
Arch Biochem Biophys
, vol.216
, Issue.1
, pp. 296-305
-
-
Hou, C.T.1
Patel, R.N.2
Laskin, A.I.3
-
38
-
-
28644443140
-
Glucagon-like peptide-1-based therapies for the treatment of Type 2 diabetes mellitus
-
Gallwitz B. Glucagon-like peptide-1-based therapies for the treatment of Type 2 diabetes mellitus. Treat Endocrinol 2005;4:361-70
-
(2005)
Treat Endocrinol
, vol.4
, pp. 361-370
-
-
Gallwitz, B.1
-
39
-
-
17144374877
-
Glucagon-like peptide 1 receptor agonists and dipeptidyl peptidase IV inhibitors: New therapeutic agents for the treatment of Type 2 diabetes
-
Sinclair EM, Drucker DJ. Glucagon-like peptide 1 receptor agonists and dipeptidyl peptidase IV inhibitors: new therapeutic agents for the treatment of Type 2 diabetes. Curr Opin Endocrinol Diabet 2005;12:146-51
-
(2005)
Curr Opin Endocrinol Diabet
, vol.12
, pp. 146-151
-
-
Sinclair, E.M.1
Drucker, D.J.2
-
40
-
-
22744449063
-
A highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of Type 2 diabetes
-
Augeri DJ, Robl JA, Betebenner DA, et al. A highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of Type 2 diabetes. J Med Chem 2005;48:5025-37
-
(2005)
J Med Chem
, vol.48
, pp. 5025-5037
-
-
Augeri, D.J.1
Robl, J.A.2
Betebenner, D.A.3
-
41
-
-
39649120688
-
-
Vu TC, Brzozowski DB, Fox R, et al. Preparation of cyclopropyl-fused pyrrolidine based inhibitors of dipeptidyl peptidase IV. WO2004052850 (2004)
-
Vu TC, Brzozowski DB, Fox R, et al. Preparation of cyclopropyl-fused pyrrolidine based inhibitors of dipeptidyl peptidase IV. WO2004052850 (2004)
-
-
-
-
42
-
-
34547223622
-
-
Hanson RL, Goldberg SL, Brzozowski DB, et al. Preparation of an amino acid intermediate for the dipeptidyl peptidase IV inhibitor, saxagliptin, using a modified phenylalanine dehydrogenase. Adv Synthesis Catalysis 2007; 349(8+9):1369-78
-
Hanson RL, Goldberg SL, Brzozowski DB, et al. Preparation of an amino acid intermediate for the dipeptidyl peptidase IV inhibitor, saxagliptin, using a modified phenylalanine dehydrogenase. Adv Synthesis Catalysis 2007; 349(8+9):1369-78
-
-
-
-
43
-
-
39649103976
-
Enzymatic synthesis of (S)-phenylalanine and related (S)-amino acids by phenylalanine dehydrogenase
-
Asano Y. Enzymatic synthesis of (S)-phenylalanine and related (S)-amino acids by phenylalanine dehydrogenase. Methods Biotechnol (Microbial Enzymes Biotransformations) 2005;17:141-50
-
(2005)
Methods Biotechnol (Microbial Enzymes Biotransformations)
, vol.17
, pp. 141-150
-
-
Asano, Y.1
-
44
-
-
29844452149
-
Engineered phenylalanine dehydrogenase in organic solvents: Homogeneous and biphasic enzymatic reactions
-
Cainelli C, Engel PC, Galletti P, et al. Engineered phenylalanine dehydrogenase in organic solvents: homogeneous and biphasic enzymatic reactions. Org Biomol Chem 2005;3(24):4316-20
-
(2005)
Org Biomol Chem
, vol.3
, Issue.24
, pp. 4316-4320
-
-
Cainelli, C.1
Engel, P.C.2
Galletti, P.3
-
45
-
-
15144353143
-
New aza-dipeptide analogs as potent and orally absorbed HIV-1 protease inhibitors: Candidates for clinical development
-
Bold G, Faessler A, Capraro H-G, et al. New aza-dipeptide analogs as potent and orally absorbed HIV-1 protease inhibitors: candidates for clinical development. J Med Chem 1998; 41(18):3387-401
-
(1998)
J Med Chem
, vol.41
, Issue.18
, pp. 3387-3401
-
-
Bold, G.1
Faessler, A.2
Capraro, H.-G.3
-
46
-
-
0033931167
-
BMS-232632, a highly potent human immunodeficiency virus protease inhibitor that can be used in combination with other available antiretroviral agents
-
Robinson BS, Riccardi KA, Gong YF, et al. BMS-232632, a highly potent human immunodeficiency virus protease inhibitor that can be used in combination with other available antiretroviral agents. Antimicrob Agents Chemother 2000;44(8):2093-9
-
(2000)
Antimicrob Agents Chemother
, vol.44
, Issue.8
, pp. 2093-2099
-
-
Robinson, B.S.1
Riccardi, K.A.2
Gong, Y.F.3
-
47
-
-
0031005587
-
Cloning, sequencing and overexpression of the leucine dehydrogenase gene from Bacillus cereus
-
Stoyan T, Recktenwald A, Kula MR. Cloning, sequencing and overexpression of the leucine dehydrogenase gene from Bacillus cereus. J Biotechnol 1997;54(1):77-80
-
(1997)
J Biotechnol
, vol.54
, Issue.1
, pp. 77-80
-
-
Stoyan, T.1
Recktenwald, A.2
Kula, M.R.3
-
48
-
-
11144346350
-
From enzymes to "designer bugs" in reductive amination: A new process for the synthesis of L-tert-leucine using a whole cell-catalyst
-
Menzel A, Werner H, Altenbuchner J, et al. From enzymes to "designer bugs" in reductive amination: a new process for the synthesis of L-tert-leucine using a whole cell-catalyst. Eng Life Sci 2004;4(6):573-6
-
(2004)
Eng Life Sci
, vol.4
, Issue.6
, pp. 573-576
-
-
Menzel, A.1
Werner, H.2
Altenbuchner, J.3
-
49
-
-
33745753963
-
A "second-generation process" for the synthesis of L-neopentylglycine: Asymmetric reductive amination using a recombinant whole cell catalyst
-
Groeger H, May O, Werner H, et al. A "second-generation process" for the synthesis of L-neopentylglycine: asymmetric reductive amination using a recombinant whole cell catalyst. Org Process Res Dev 2006;10(3):666-9
-
(2006)
Org Process Res Dev
, vol.10
, Issue.3
, pp. 666-669
-
-
Groeger, H.1
May, O.2
Werner, H.3
-
51
-
-
14644431841
-
N-methyl-L-amino acid dehydrogenase from Pseudomonas putida. A novel member of an unusual NAD(P)-dependent oxidoreductase superfamily
-
Mihara H, Muramatsu H, Kakutani R, et al. N-methyl-L-amino acid dehydrogenase from Pseudomonas putida. A novel member of an unusual NAD(P)-dependent oxidoreductase superfamily. FEBS J 2005; 272(50):1117-23
-
(2005)
FEBS J
, vol.272
, Issue.50
, pp. 1117-1123
-
-
Mihara, H.1
Muramatsu, H.2
Kakutani, R.3
-
52
-
-
0030568596
-
Stereoselective synthesis of opine-type secondary amine carboxylic acids by a new enzyme opine dehydrogenase. Use of recombinant enzymes
-
Kato Y, Yamada H, Asano Y. Stereoselective synthesis of opine-type secondary amine carboxylic acids by a new enzyme opine dehydrogenase. Use of recombinant enzymes. J Mol Catalysis B Enzymatic 1996;1(3-6):151-60
-
(1996)
J Mol Catalysis B Enzymatic
, vol.1
, Issue.3-6
, pp. 151-160
-
-
Kato, Y.1
Yamada, H.2
Asano, Y.3
-
53
-
-
20644464337
-
Use of GNRH antagonists in reproductive medicine
-
Merviel P, Najas S, Campy H, et al. Use of GNRH antagonists in reproductive medicine. Minerva Ginecol 2005;57(1):29-43
-
(2005)
Minerva Ginecol
, vol.57
, Issue.1
, pp. 29-43
-
-
Merviel, P.1
Najas, S.2
Campy, H.3
-
54
-
-
0035712804
-
Pharmacokinetics of an emerging new class of anticoagulant antithrombotic drugs. A review of small-molecule thrombin inhibitors
-
Hauptmann J. Pharmacokinetics of an emerging new class of anticoagulant antithrombotic drugs. A review of small-molecule thrombin inhibitors. Eur J Clin Pharmacol 2002; 57(11):751-58
-
(2002)
Eur J Clin Pharmacol
, vol.57
, Issue.11
, pp. 751-758
-
-
Hauptmann, J.1
-
55
-
-
0036900263
-
The production of fine chemicals by biotransformations
-
Straathof AJJ, Panke SA. The production of fine chemicals by biotransformations. Curr Opin Bin technol 2002; 13(6):548-56
-
(2002)
Curr Opin Bin technol
, vol.13
, Issue.6
, pp. 548-556
-
-
Straathof, A.J.J.1
Panke, S.A.2
-
56
-
-
0032530505
-
Biocatalysis to amino acid-based chiral pharmaceuticals-examples and perspectives
-
Bommarius AS, Schwarm M, Drauz K. Biocatalysis to amino acid-based chiral pharmaceuticals-examples and perspectives. J Mol Catalysis B Enzymatic 1998;5(1-4):1-11
-
(1998)
J Mol Catalysis B Enzymatic
, vol.5
, Issue.1-4
, pp. 1-11
-
-
Bommarius, A.S.1
Schwarm, M.2
Drauz, K.3
-
57
-
-
33747808618
-
Creation of a broad-range and highly Stereoselective D-amino acid dehydrogenase for the one-step synthesis of D-amino acids
-
Vedha PK, Gunawardana M, Rozzell DJ, et al. Creation of a broad-range and highly Stereoselective D-amino acid dehydrogenase for the one-step synthesis of D-amino acids. J Am Chem Soc 2006; 128(33):10923-9
-
(2006)
J Am Chem Soc
, vol.128
, Issue.33
, pp. 10923-10929
-
-
Vedha, P.K.1
Gunawardana, M.2
Rozzell, D.J.3
-
58
-
-
0029866371
-
Effects of inogatran, a new low-molecular-weight thrombin inhibitor, in rat models of venous and arterial thrombosis, thrombolysis and bleeding time
-
Gustafsson D, Elg M, Lenfors S, et al. Effects of inogatran, a new low-molecular-weight thrombin inhibitor, in rat models of venous and arterial thrombosis, thrombolysis and bleeding time. Blood Coagul Fibrinolysis 1996; 7(1):69-79
-
(1996)
Blood Coagul Fibrinolysis
, vol.7
, Issue.1
, pp. 69-79
-
-
Gustafsson, D.1
Elg, M.2
Lenfors, S.3
-
59
-
-
0347526452
-
Diastereoselective microbial reduction of (S)-[3-chloro-2-oxo-1 (phenylmethyl) propyl]carbamic acid, 1,1-dimethylethyl ester
-
Patel RN, Chu L, Mueller RH. Diastereoselective microbial reduction of (S)-[3-chloro-2-oxo-1 (phenylmethyl) propyl]carbamic acid, 1,1-dimethylethyl ester. Tetrahedron:Asymmetry 2003; 14(20):3105-9
-
(2003)
Tetrahedron:Asymmetry
, vol.14
, Issue.20
, pp. 3105-3109
-
-
Patel, R.N.1
Chu, L.2
Mueller, R.H.3
-
60
-
-
0024803411
-
Metabolism of the antianxiety drug buspirone in human subjects
-
Jajoo HK, Mayol RF, LaBudde JA, et al. Metabolism of the antianxiety drug buspirone in human subjects. Drug Metab Dispos 1989;17(6):634-40
-
(1989)
Drug Metab Dispos
, vol.17
, Issue.6
, pp. 634-640
-
-
Jajoo, H.K.1
Mayol, R.F.2
LaBudde, J.A.3
-
61
-
-
39649117229
-
-
Mayol RF. Buspirone metabolite for the alleviation of anxiety. US6150365 2000
-
Mayol RF. Buspirone metabolite for the alleviation of anxiety. US6150365 (2000)
-
-
-
-
62
-
-
0027080120
-
Synthesis and biological characterization of α-(4-fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-1-piperazinebutanol and analogs as potential atypical antipsychotic agents
-
Yevich JP, New JS, Lobeck WG, et al. Synthesis and biological characterization of α-(4-fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-1-piperazinebutanol and analogs as potential atypical antipsychotic agents. J Med Chem 1992;35(24):4516-25
-
(1992)
J Med Chem
, vol.35
, Issue.24
, pp. 4516-4525
-
-
Yevich, J.P.1
New, J.S.2
Lobeck, W.G.3
-
63
-
-
39649118110
-
-
Yevich JP, Mayol RF, Li J, et al, S)-6-Hydroxy-buspirone for treatment of anxiety, depression and related disorders. US2003022899 2003
-
Yevich JP, Mayol RF, Li J, et al. (S)-6-Hydroxy-buspirone for treatment of anxiety, depression and related disorders. US2003022899 (2003)
-
-
-
-
64
-
-
24044496549
-
Enantioselective microbial reduction of 6-oxo-8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5] decane-7,9-dione
-
Patel RN, Chu L, Nanduri V, et al. Enantioselective microbial reduction of 6-oxo-8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5] decane-7,9-dione. Tetrahedron:Asymmetry 2005;16(16):2778-83
-
(2005)
Tetrahedron:Asymmetry
, vol.16
, Issue.16
, pp. 2778-2783
-
-
Patel, R.N.1
Chu, L.2
Nanduri, V.3
-
65
-
-
33748750991
-
Enantioselective microbial reduction of 6-oxo-8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5] decane-7,9-dione: Cloning and expression of reductases
-
Goldberg SL, Nanduri VB, Chu L, et al. Enantioselective microbial reduction of 6-oxo-8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5] decane-7,9-dione: cloning and expression of reductases. Enzyme Microb Technol 2006;39(7):1441-50
-
(2006)
Enzyme Microb Technol
, vol.39
, Issue.7
, pp. 1441-1450
-
-
Goldberg, S.L.1
Nanduri, V.B.2
Chu, L.3
-
66
-
-
24744437999
-
Discovery of a 1H-benzoimidazol-2-yl-1H-pyridin-2-one (BMS-536924) inhibitor of insulin-like growth factor I receptor kinase with in vivo antitumor activity
-
Wittman M, Carboni J, Attar R, et al. Discovery of a 1H-benzoimidazol-2-yl-1H-pyridin-2-one (BMS-536924) inhibitor of insulin-like growth factor I receptor kinase with in vivo antitumor activity. J Med Chem 2005;48(18):5639-43
-
(2005)
J Med Chem
, vol.48
, Issue.18
, pp. 5639-5643
-
-
Wittman, M.1
Carboni, J.2
Attar, R.3
-
67
-
-
33846607237
-
Novel 1H-(benzimidazol-2-yl)-1H-pyridin-2-one inhibitors of insulin-like growth factor I (IGF-1R) kinase
-
Wittman MD, Balasubramanian B, Stoffan K, et al. Novel 1H-(benzimidazol-2-yl)-1H-pyridin-2-one inhibitors of insulin-like growth factor I (IGF-1R) kinase. Bioorg Med Chem Lett 2007; 17(4);974-7
-
(2007)
Bioorg Med Chem Lett
, vol.17
, Issue.4
, pp. 974-977
-
-
Wittman, M.D.1
Balasubramanian, B.2
Stoffan, K.3
-
68
-
-
20544475647
-
-
Hanson RL, Goldberg S, Goswami A, et al. Purification and cloning of a ketoreductase used for the preparation of chiral alcohols. Adv Synthesis Catalysis 2005; 347(7+8):1073-80
-
Hanson RL, Goldberg S, Goswami A, et al. Purification and cloning of a ketoreductase used for the preparation of chiral alcohols. Adv Synthesis Catalysis 2005; 347(7+8):1073-80
-
-
-
-
69
-
-
0027897733
-
Enantioselective microbial reduction of 3,5-dioxo-6-(benzyloxy) hexanoic acid, ethyl ester
-
Patel RN, Banerjee A, McNamee CC, et al. Enantioselective microbial reduction of 3,5-dioxo-6-(benzyloxy) hexanoic acid, ethyl ester. Enzyme Microb Technol 1993;15(12):1014-21
-
(1993)
Enzyme Microb Technol
, vol.15
, Issue.12
, pp. 1014-1021
-
-
Patel, R.N.1
Banerjee, A.2
McNamee, C.C.3
-
70
-
-
0036986060
-
The discovery and development of atorvastatin, a potent novel hypolipidemic agent
-
Roth BD. The discovery and development of atorvastatin, a potent novel hypolipidemic agent. Prog Med Chem 2002;40:1-22
-
(2002)
Prog Med Chem
, vol.40
, pp. 1-22
-
-
Roth, B.D.1
-
71
-
-
33745357176
-
Synthesis of ethyl and t-butyl (3R,5S)-dihydroxy-6-benzyloxy hexanoates via diastereo- and enantioselective microbial reduction
-
Guo Z, Chen Y, Goswami A, et al. Synthesis of ethyl and t-butyl (3R,5S)-dihydroxy-6-benzyloxy hexanoates via diastereo- and enantioselective microbial reduction. Tetrahedron:Asymmetry 2006;17(1):1589-602
-
(2006)
Tetrahedron:Asymmetry
, vol.17
, Issue.1
, pp. 1589-1602
-
-
Guo, Z.1
Chen, Y.2
Goswami, A.3
-
72
-
-
0033859659
-
New advances in the discovery of thrombin and factor Xa inhibitors
-
Vacca JP. New advances in the discovery of thrombin and factor Xa inhibitors. Curr Opin Chem Biol 2000;4(4):394-400
-
(2000)
Curr Opin Chem Biol
, vol.4
, Issue.4
, pp. 394-400
-
-
Vacca, J.P.1
-
73
-
-
0036161816
-
Bivalirudin. A direct thrombin inhibitor
-
Gladwell TD. Bivalirudin. A direct thrombin inhibitor. Clin Ther 2002;24(1):38-58
-
(2002)
Clin Ther
, vol.24
, Issue.1
, pp. 38-58
-
-
Gladwell, T.D.1
-
74
-
-
77956750628
-
Anticoagulants: Thrombin and factor Xa inhibitors
-
Fevig JM, Wexler RR. Anticoagulants: thrombin and factor Xa inhibitors. Annu Rep Med Chem 1999;34:81-100
-
(1999)
Annu Rep Med Chem
, vol.34
, pp. 81-100
-
-
Fevig, J.M.1
Wexler, R.R.2
-
75
-
-
39649087894
-
-
Williams PD, Coburn C, Burgey C, et al. Preparation of triazolopyrimidines as thrombin inhibitors. WO2002064211 (2002)
-
Williams PD, Coburn C, Burgey C, et al. Preparation of triazolopyrimidines as thrombin inhibitors. WO2002064211 (2002)
-
-
-
-
76
-
-
2542468051
-
Stereoselective synthesis of a potent thrombin inhibitor by a novel P2-P3 lactone ring opening
-
Nelson TD, LeBlond CR, Frantz DE, et al. Stereoselective synthesis of a potent thrombin inhibitor by a novel P2-P3 lactone ring opening. J Org Chem 2004;69(11):3620-7
-
(2004)
J Org Chem
, vol.69
, Issue.11
, pp. 3620-3627
-
-
Nelson, T.D.1
LeBlond, C.R.2
Frantz, D.E.3
-
77
-
-
0024369162
-
Retinobenzoic acids. 1. Structure-activity relationships of aromatic amides with retinoidal activity
-
Kagechika H, Kawachi E, Hashimoto Y, et al. Retinobenzoic acids. 1. Structure-activity relationships of aromatic amides with retinoidal activity. J Med Chem 1989;32(12):2583-8
-
(1989)
J Med Chem
, vol.32
, Issue.12
, pp. 2583-2588
-
-
Kagechika, H.1
Kawachi, E.2
Hashimoto, Y.3
-
78
-
-
39649115085
-
Retinoids. Vitamin A for clinical applications
-
Kagechika H, Shudo K. Retinoids. Vitamin A for clinical applications. Farumashia 1990;26:35-40
-
(1990)
Farumashia
, vol.26
, pp. 35-40
-
-
Kagechika, H.1
Shudo, K.2
-
79
-
-
77956833990
-
Retinoids: Their physiological function and therapeutic potential
-
Morriss-Kay GM. Retinoids: their physiological function and therapeutic potential. Adv Organ Biol 1997;3:79
-
(1997)
Adv Organ Biol
, vol.3
, pp. 79
-
-
Morriss-Kay, G.M.1
-
80
-
-
0022839127
-
Anticarcinogenic effects of retinoids in animals
-
Moon RC, Mehta RG. Anticarcinogenic effects of retinoids in animals. Adv Exp Med Biol 1986;206:399-411
-
(1986)
Adv Exp Med Biol
, vol.206
, pp. 399-411
-
-
Moon, R.C.1
Mehta, R.G.2
-
81
-
-
0037155676
-
-
Patel RN, Chu L, Chidambaram R, et al. Enantioselective microbial reduction of 2-oxo-2-(1′,2′,3′,4′-tetrahydro- 1′,1′,4′,4′-tetramethyl- 6′-naphthalenyl)acetic acid and its ethyl ester. Tetrahedron:Asymmetry 2002;13(4):349-55
-
Patel RN, Chu L, Chidambaram R, et al. Enantioselective microbial reduction of 2-oxo-2-(1′,2′,3′,4′-tetrahydro- 1′,1′,4′,4′-tetramethyl- 6′-naphthalenyl)acetic acid and its ethyl ester. Tetrahedron:Asymmetry 2002;13(4):349-55
-
-
-
-
82
-
-
0031638091
-
Enhancement of pulmonary artery contraction induced by endothelin-β receptor antagonism
-
Fukuroda T, Nishikibe M. Enhancement of pulmonary artery contraction induced by endothelin-β receptor antagonism. J Cardiovasc Pharmacol 1998;31:169-71
-
(1998)
J Cardiovasc Pharmacol
, vol.31
, pp. 169-171
-
-
Fukuroda, T.1
Nishikibe, M.2
-
83
-
-
0026615759
-
Endothelin ETA and ETB receptors mediate vascular smooth muscle contraction
-
Sumner MJ, Cannon TR, Mundin JW, et al. Endothelin ETA and ETB receptors mediate vascular smooth muscle contraction. Br J Pharmacol 1992;107(3):858-60
-
(1992)
Br J Pharmacol
, vol.107
, Issue.3
, pp. 858-860
-
-
Sumner, M.J.1
Cannon, T.R.2
Mundin, J.W.3
-
84
-
-
0035203285
-
Asymmetric biosynthesis of key aromatic intermediates in the synthesis of an endothelin receptor antagonist
-
Krulewicz B, Tschaen D, Devine P, et al. Asymmetric biosynthesis of key aromatic intermediates in the synthesis of an endothelin receptor antagonist. Biocatalysis Biotransformation 2001; 19(4):267-79
-
(2001)
Biocatalysis Biotransformation
, vol.19
, Issue.4
, pp. 267-279
-
-
Krulewicz, B.1
Tschaen, D.2
Devine, P.3
-
85
-
-
85127651620
-
Semisynthesis of taxol and taxotere
-
Suffness M, editor, CRC Press, NY
-
Holton R, Biediger R, Boatman D. Semisynthesis of taxol and taxotere. In: Taxol: Science and Application. Suffness M, editor, CRC Press, NY. 1995. p. 97-121
-
(1995)
Taxol: Science and Application
, pp. 97-121
-
-
Holton, R.1
Biediger, R.2
Boatman, D.3
-
86
-
-
0031754884
-
Tour de paclitaxel: Biocatalysis for semisynthesis
-
Patel RN. Tour de paclitaxel: biocatalysis for semisynthesis. Annu Rev Microbiol 1995;98:361-95
-
(1995)
Annu Rev Microbiol
, vol.98
, pp. 361-395
-
-
Patel, R.N.1
-
87
-
-
0027176327
-
Microbial synthesis of (2R,3S)-(-)-N-benzoyl-3-phenyl isoserine ethyl ester, a taxol side-chain synthon
-
Patel RN, Banerjee A, Howell JM, et al. Microbial synthesis of (2R,3S)-(-)-N-benzoyl-3-phenyl isoserine ethyl ester, a taxol side-chain synthon. Tetrahedron: Asymmetry 1993;4(9):2069-84
-
(1993)
Tetrahedron: Asymmetry
, vol.4
, Issue.9
, pp. 2069-2084
-
-
Patel, R.N.1
Banerjee, A.2
Howell, J.M.3
-
88
-
-
0024355566
-
Drugs acting on sigma and phencyclidine receptors: A review of their nature, function, and possible therapeutic importance
-
Junien JL, Leonard BE. Drugs acting on sigma and phencyclidine receptors: a review of their nature, function, and possible therapeutic importance. Clin Neuropharmacol 1989;12(5);353-74
-
(1989)
Clin Neuropharmacol
, vol.12
, Issue.5
, pp. 353-374
-
-
Junien, J.L.1
Leonard, B.E.2
-
89
-
-
0026347822
-
σ Receptors: From molecule to man
-
Ferris, CD, Hirsch DJ, Brooks BP, et al. σ Receptors: from molecule to man. J Neurochem 1991;57(3):729-37
-
(1991)
J Neurochem
, vol.57
, Issue.3
, pp. 729-737
-
-
Ferris, C.D.1
Hirsch, D.J.2
Brooks, B.P.3
-
90
-
-
84981976205
-
Microbial reduction of 1-(4-fluorophenyl)-4-[4-(5-fluoro-2-pyrimidinyl)-1-piperazinyl] butan-1-one
-
Patel RN, Banerjee A, Liu M, et al. Microbial reduction of 1-(4-fluorophenyl)-4-[4-(5-fluoro-2-pyrimidinyl)-1-piperazinyl] butan-1-one. Biotechnol Appl Biochem 1993;17(2):139-53
-
(1993)
Biotechnol Appl Biochem
, vol.17
, Issue.2
, pp. 139-153
-
-
Patel, R.N.1
Banerjee, A.2
Liu, M.3
-
91
-
-
4544384606
-
Nonpeptide α vβ 3 antagonists. Part 11. Discovery and preclinical evaluation of potent α vβ 3 antagonists for the prevention and treatment of osteoporosis
-
Coleman PJ, Brashear KM, Askew BC, Nonpeptide α vβ 3 antagonists. Part 11. Discovery and preclinical evaluation of potent α vβ 3 antagonists for the prevention and treatment of osteoporosis. J Med Chem 2004;47(20):4829-37
-
(2004)
J Med Chem
, vol.47
, Issue.20
, pp. 4829-4837
-
-
Coleman, P.J.1
Brashear, K.M.2
Askew, B.C.3
-
92
-
-
33644889382
-
Asymmetric reduction of alpha, beta-unsaturated ketone to (R) allylic alcohol by Candida chilensis
-
Pollard DJ, Telari K, Lane J et al. Asymmetric reduction of alpha, beta-unsaturated ketone to (R) allylic alcohol by Candida chilensis. Biotechnol Bioeng 2006;93:674-86
-
(2006)
Biotechnol Bioeng
, vol.93
, pp. 674-686
-
-
Pollard, D.J.1
Telari, K.2
Lane, J.3
-
93
-
-
0037467063
-
Efficient synthesis of NK1 receptor antagonist aprepitant using a crystallization - induced diastereoselective transformation
-
Brands KMJ, Payack JF, Rosen JD, et al. Efficient synthesis of NK1 receptor antagonist aprepitant using a crystallization - induced diastereoselective transformation. J Am Chem Soc 2003;125(8):2129-35
-
(2003)
J Am Chem Soc
, vol.125
, Issue.8
, pp. 2129-2135
-
-
Brands, K.M.J.1
Payack, J.F.2
Rosen, J.D.3
-
94
-
-
33645922462
-
Effective synthesis of (S)-3,5-bistrifluoro methylphenyl ethanol by asymmetric enzymatic reduction
-
Pollard D, Truppo M, Pollard J, et al. Effective synthesis of (S)-3,5-bistrifluoro methylphenyl ethanol by asymmetric enzymatic reduction. Tetrahedron:Asymmetry 2006;17(4):554-9
-
(2006)
Tetrahedron:Asymmetry
, vol.17
, Issue.4
, pp. 554-559
-
-
Pollard, D.1
Truppo, M.2
Pollard, J.3
-
95
-
-
33846629495
-
Enzyme-catalyzed enantioselective diaryl ketone reductions
-
Truppo MD, Pollard D, Devine P. Enzyme-catalyzed enantioselective diaryl ketone reductions. Org Lett 2007; 9(2):335-8
-
(2007)
Org Lett
, vol.9
, Issue.2
, pp. 335-338
-
-
Truppo, M.D.1
Pollard, D.2
Devine, P.3
-
96
-
-
0033934330
-
Treatment of hepatitis C with interferon and ribavirin
-
Pianko S, McHutchison JG. Treatment of hepatitis C with interferon and ribavirin. J Gastroenterol Hepatol 2000;15(6):581-6
-
(2000)
J Gastroenterol Hepatol
, vol.15
, Issue.6
, pp. 581-586
-
-
Pianko, S.1
McHutchison, J.G.2
-
97
-
-
0034763066
-
Combination of interferon induction therapy and ribavirin in chronic hepatitis C
-
Ferenci P, Brunner H, Nachbaur K, et al. Combination of interferon induction therapy and ribavirin in chronic hepatitis C. Hepatology 2001;34(5):1006-11
-
(2001)
Hepatology
, vol.34
, Issue.5
, pp. 1006-1011
-
-
Ferenci, P.1
Brunner, H.2
Nachbaur, K.3
-
98
-
-
0034798908
-
Comparative effects of different doses of ribavirin plus interferon-α2b for therapy of chronic hepatitis C: Results of a controlled, randomized trial
-
Bonkovsky HL, Stefancyk D, McNeal K, et al. Comparative effects of different doses of ribavirin plus interferon-α2b for therapy of chronic hepatitis C: results of a controlled, randomized trial. Dig Dis Sci 2001;46(10):2051-9
-
(2001)
Dig Dis Sci
, vol.46
, Issue.10
, pp. 2051-2059
-
-
Bonkovsky, H.L.1
Stefancyk, D.2
McNeal, K.3
-
99
-
-
0347365747
-
Pilot-scale lipase-catalyzed regioselective acylation of ribavirin in anhydrous media in the synthesis of a novel prodrug intermediate
-
Tamarez M, Morgan B, Wong GSK, et al. Pilot-scale lipase-catalyzed regioselective acylation of ribavirin in anhydrous media in the synthesis of a novel prodrug intermediate. Org Proc Res Dev 2003;7(6):951-3
-
(2003)
Org Proc Res Dev
, vol.7
, Issue.6
, pp. 951-953
-
-
Tamarez, M.1
Morgan, B.2
Wong, G.S.K.3
-
100
-
-
0030873624
-
A very short, efficient and inexpensive synthesis of the prodrug form of SC-54701A a platelet aggregation inhibitor
-
Cossy J, Schmitt A, Cinquin C, et al. A very short, efficient and inexpensive synthesis of the prodrug form of SC-54701A a platelet aggregation inhibitor. Bioorg Med Chem Lett 1997;7(13):1699-700
-
(1997)
Bioorg Med Chem Lett
, vol.7
, Issue.13
, pp. 1699-1700
-
-
Cossy, J.1
Schmitt, A.2
Cinquin, C.3
-
101
-
-
1542268869
-
An efficient synthesis of the orally-active GpIIb/IIIa antagonist FR184764
-
Yamanaka T, Ohkubo M, Takahashi F, et al. An efficient synthesis of the orally-active GpIIb/IIIa antagonist FR184764. Tetrahedron Lett 2004;45(13):2843-5
-
(2004)
Tetrahedron Lett
, vol.45
, Issue.13
, pp. 2843-2845
-
-
Yamanaka, T.1
Ohkubo, M.2
Takahashi, F.3
-
102
-
-
0036330143
-
Kinetic resolution of β-amino esters by acylation using immobilized penicillin amidohydrolase
-
Landis BH, Mullins PB, Mullins KB, et al. Kinetic resolution of β-amino esters by acylation using immobilized penicillin amidohydrolase. Org Proc Res Dev 2002;6(4):539-46
-
(2002)
Org Proc Res Dev
, vol.6
, Issue.4
, pp. 539-546
-
-
Landis, B.H.1
Mullins, P.B.2
Mullins, K.B.3
-
103
-
-
7844233665
-
(+)-4-[2-[4-(8-Chloro-3, 10-dibromo-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]-pyridin-11 (R)-yl)-1-piperidinyl]-2-oxoethyl]-1-piperidinecarboxamide (SCH-66336): A very potent farnesyl protein transferase inhibitor as a novel antitumor agent
-
Njoroge FG, Taveras AG, Kelly J, et al. (+)-4-[2-[4-(8-Chloro-3, 10-dibromo-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]-pyridin-11 (R)-yl)-1-piperidinyl]-2-oxoethyl]-1-piperidinecarboxamide (SCH-66336): a very potent farnesyl protein transferase inhibitor as a novel antitumor agent. J Med Chem 1998;41:4890-902
-
(1998)
J Med Chem
, vol.41
, pp. 4890-4902
-
-
Njoroge, F.G.1
Taveras, A.G.2
Kelly, J.3
-
104
-
-
0033828991
-
Enzymatic kinetic resolution of piperidine atropisomers: Synthesis of a key intermediate of the farnesyl protein transferase inhibitor, SCH66336
-
Morgan B, Zaks A, Dodds DR, et al. Enzymatic kinetic resolution of piperidine atropisomers: synthesis of a key intermediate of the farnesyl protein transferase inhibitor, SCH66336. J Org Chem 2000;65(18):5451-9
-
(2000)
J Org Chem
, vol.65
, Issue.18
, pp. 5451-5459
-
-
Morgan, B.1
Zaks, A.2
Dodds, D.R.3
-
106
-
-
0033757127
-
Regioselective enzymatic aminoacylation of lobucavir to give an intermediate for lobucavir prodrug
-
Hanson RL, Shi Z, Brzozowski DB, et al. Regioselective enzymatic aminoacylation of lobucavir to give an intermediate for lobucavir prodrug. Bioorg Med Chem 2000;8(12):2681-7
-
(2000)
Bioorg Med Chem
, vol.8
, Issue.12
, pp. 2681-2687
-
-
Hanson, R.L.1
Shi, Z.2
Brzozowski, D.B.3
-
107
-
-
0019841289
-
Structure of an antitumor antibiotic, spergaulin
-
Umezawa H, Kondo S, Iinuma H, et al. Structure of an antitumor antibiotic, spergaulin. J Antibiot 1981;34(12):1622-4
-
(1981)
J Antibiot
, vol.34
, Issue.12
, pp. 1622-1624
-
-
Umezawa, H.1
Kondo, S.2
Iinuma, H.3
-
108
-
-
0023638940
-
Synthesis and antitumor activity of spergualin analogues. III. Novel method for synthesis of optically active 15-deoxyspergualin and 15-deoxy-11-O-methylspergualin
-
Umeda Y, Moriguchi M, Ikai K, et al. Synthesis and antitumor activity of spergualin analogues. III. Novel method for synthesis of optically active 15-deoxyspergualin and 15-deoxy-11-O-methylspergualin. J Antibiot 1987;40(9):1316-24
-
(1987)
J Antibiot
, vol.40
, Issue.9
, pp. 1316-1324
-
-
Umeda, Y.1
Moriguchi, M.2
Ikai, K.3
-
109
-
-
0030937175
-
Stereoselective acetylation of [1-(hydroxy)-4-(3-phenoxyphenyl)butyl] phosphonic acid diethyl ester
-
Patel RN, Banerjee A, Szarka LJ. Stereoselective acetylation of [1-(hydroxy)-4-(3-phenoxyphenyl)butyl] phosphonic acid diethyl ester. Tetrahedron:Asymmetry 1997; 8(7):1055-9
-
(1997)
Tetrahedron:Asymmetry
, vol.8
, Issue.7
, pp. 1055-1059
-
-
Patel, R.N.1
Banerjee, A.2
Szarka, L.J.3
-
110
-
-
0027260855
-
Synthesis and background chemistry of 15-deoxyspergualin
-
Maeda K, Umeda Y, Saino T. Synthesis and background chemistry of 15-deoxyspergualin. Ann NY Acad Sci 1993;685:123-35
-
(1993)
Ann NY Acad Sci
, vol.685
, pp. 123-135
-
-
Maeda, K.1
Umeda, Y.2
Saino, T.3
-
111
-
-
0025000298
-
Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors
-
Sit SY, Parker BA, Motoc I, et al. Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors. J Med Chem 1990;33(11):2982-99
-
(1990)
J Med Chem
, vol.33
, Issue.11
, pp. 2982-2999
-
-
Sit, S.Y.1
Parker, B.A.2
Motoc, I.3
-
112
-
-
0026485637
-
Enantioselective enzymic acetylation of racemic [4-[4α,6β(E)]]-6-[4,4-bis (4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl] tetrahydro-4-hydroxy-2H-pyran-2-one
-
Patel RN, McNamee CM, Szarka LJ. Enantioselective enzymic acetylation of racemic [4-[4α,6β(E)]]-6-[4,4-bis (4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl] tetrahydro-4-hydroxy-2H-pyran-2-one. Appl Microbiol Biotechnol 1992;38:56-60
-
(1992)
Appl Microbiol Biotechnol
, vol.38
, pp. 56-60
-
-
Patel, R.N.1
McNamee, C.M.2
Szarka, L.J.3
-
113
-
-
0035169318
-
Potential treatment opportunities for Alzheimer's disease through inhibition of secretases and Aβ immunization
-
Schenk D, Games D, Seubert P. Potential treatment opportunities for Alzheimer's disease through inhibition of secretases and Aβ immunization. J Mol Neurosci 2001;17(2):259-67
-
(2001)
J Mol Neurosci
, vol.17
, Issue.2
, pp. 259-267
-
-
Schenk, D.1
Games, D.2
Seubert, P.3
-
114
-
-
39649120439
-
-
Audia JE, James E, Britton TC, et al. Preparation of N-(phenylacetyl) di- and tripeptide derivatives for inhibiting β-amyloid peptide release. WO9822494 (1998)
-
Audia JE, James E, Britton TC, et al. Preparation of N-(phenylacetyl) di- and tripeptide derivatives for inhibiting β-amyloid peptide release. WO9822494 (1998)
-
-
-
-
115
-
-
0034300323
-
Enzymatic resolution of racemic secondary alcohols by lipase B from Candida antarctica
-
Patel RN, Banerjee A, Nanduri VB, et al. Enzymatic resolution of racemic secondary alcohols by lipase B from Candida antarctica. J Am Oil Chem Soc 2000;77(10):1015-9
-
(2000)
J Am Oil Chem Soc
, vol.77
, Issue.10
, pp. 1015-1019
-
-
Patel, R.N.1
Banerjee, A.2
Nanduri, V.B.3
-
116
-
-
39649105120
-
-
Bisacchi G, Slusarchyk WA, Treuner U, et al. Preparation of amidino and guanidine azetidinone compounds as tryptase inhibitors. WO9967215 (1999)
-
Bisacchi G, Slusarchyk WA, Treuner U, et al. Preparation of amidino and guanidine azetidinone compounds as tryptase inhibitors. WO9967215 (1999)
-
-
-
-
117
-
-
0035614127
-
Chemical and enzymatic resolution of (R,S)-N-(tert-butoxycarbonyl)-3-hydroxymethylpiperidine
-
Goswami A, Howell JM, Hua EY, et al. Chemical and enzymatic resolution of (R,S)-N-(tert-butoxycarbonyl)-3-hydroxymethylpiperidine. Org Proc Res Dev 2001;5(4):415-20
-
(2001)
Org Proc Res Dev
, vol.5
, Issue.4
, pp. 415-420
-
-
Goswami, A.1
Howell, J.M.2
Hua, E.Y.3
-
118
-
-
0034029015
-
Aromatic hydrocarbon dioxygenases in environmental biotechnology
-
Gibson DT, Parales RE. Aromatic hydrocarbon dioxygenases in environmental biotechnology. Curr Opin Biotech 2000;11(3):236-43
-
(2000)
Curr Opin Biotech
, vol.11
, Issue.3
, pp. 236-243
-
-
Gibson, D.T.1
Parales, R.E.2
-
119
-
-
84944760802
-
Applications of aromatic hydrocarbon dioxygenases
-
Patel RN, editor, CRC Press, FL
-
Parales RE, Resnick SM. Applications of aromatic hydrocarbon dioxygenases. Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 299-331
-
(2007)
Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 299-331
-
-
Parales, R.E.1
Resnick, S.M.2
-
121
-
-
85047699463
-
Purification, crystallization and preliminary X-ray diffraction studies of the three components of the toluene 2,3-dioxygenase enzyme system
-
Lee K, Friemann R, Parales JV, et al. Purification, crystallization and preliminary X-ray diffraction studies of the three components of the toluene 2,3-dioxygenase enzyme system. Acta Crystallograph Sect F Struct Biol Cryst Commun F61 2005;7:669-72
-
(2005)
Acta Crystallograph Sect F Struct Biol Cryst Commun
, vol.F61
, Issue.7
, pp. 669-672
-
-
Lee, K.1
Friemann, R.2
Parales, J.V.3
-
122
-
-
0347264753
-
Crystal structure of naphthalene dioxygenase: Side-on binding of dioxygen to iron
-
Karlsson A, Parales JV, Parales RE, et al. Crystal structure of naphthalene dioxygenase: side-on binding of dioxygen to iron. Science 2003; 299(5609):1039-42
-
(2003)
Science
, vol.299
, Issue.5609
, pp. 1039-1042
-
-
Karlsson, A.1
Parales, J.V.2
Parales, R.E.3
-
123
-
-
0001846314
-
Enzymatic dihydroxylation of aromatics in enantioselective synthesis: Expanding asymmetric methodology
-
Hudlicky T, Gonzalez D, Gibson DT. Enzymatic dihydroxylation of aromatics in enantioselective synthesis: expanding asymmetric methodology. Aldrichimica Acta 1999;32(2):35-62
-
(1999)
Aldrichimica Acta
, vol.32
, Issue.2
, pp. 35-62
-
-
Hudlicky, T.1
Gonzalez, D.2
Gibson, D.T.3
-
124
-
-
0035711112
-
Aromatic dioxygenases: Molecular biocatalysis and applications
-
Boyd DR, Sharma ND, Allen CCR. Aromatic dioxygenases: molecular biocatalysis and applications. Curr Opin Biotechnol 2001; 12(6):564-73
-
(2001)
Curr Opin Biotechnol
, vol.12
, Issue.6
, pp. 564-573
-
-
Boyd, D.R.1
Sharma, N.D.2
Allen, C.C.R.3
-
125
-
-
33645677539
-
Arene cis-dihydrodiol formation: From biology to application
-
Boyd DR, Bugg TDH. Arene cis-dihydrodiol formation: from biology to application. Org Biomol Chem 2006;4(2):181-92
-
(2006)
Org Biomol Chem
, vol.4
, Issue.2
, pp. 181-192
-
-
Boyd, D.R.1
Bugg, T.D.H.2
-
126
-
-
34547212769
-
Enzyme-catalysed synthesis and absolute configuration assignments of cis-dihydrodiol metabolites from 1,4-disubstituted benzenes
-
Boyd DR, Sharma ND, Coen GP, et al. Enzyme-catalysed synthesis and absolute configuration assignments of cis-dihydrodiol metabolites from 1,4-disubstituted benzenes. Chem A Eur J 2007;13(20):5804-11
-
(2007)
Chem A Eur J
, vol.13
, Issue.20
, pp. 5804-5811
-
-
Boyd, D.R.1
Sharma, N.D.2
Coen, G.P.3
-
127
-
-
0005470103
-
Bioconversion of indene to cis-(1S,2R)-indandiol and trans-(1R,2R)-indandiol by Rhodococcus sp
-
Chartrain M, Jackey B, Taylor C, et al. Bioconversion of indene to cis-(1S,2R)-indandiol and trans-(1R,2R)-indandiol by Rhodococcus sp. J Ferment Technol 1998;86:550-8
-
(1998)
J Ferment Technol
, vol.86
, pp. 550-558
-
-
Chartrain, M.1
Jackey, B.2
Taylor, C.3
-
128
-
-
0033943997
-
Biocatalysis for pharmaceuticals-status and prospects for a key technology
-
Buckland BC, Robinson DK, Chartrain M. Biocatalysis for pharmaceuticals-status and prospects for a key technology. Metab Eng 2000;2:42-8
-
(2000)
Metab Eng
, vol.2
, pp. 42-48
-
-
Buckland, B.C.1
Robinson, D.K.2
Chartrain, M.3
-
129
-
-
0034026210
-
Metabolic engineering and directed evolution for the production of pharmaceuticals
-
Chartrain M, Salmon PM, Robinson DK, et al. Metabolic engineering and directed evolution for the production of pharmaceuticals. Curr Opin Biotechnol 2000;11:209-14
-
(2000)
Curr Opin Biotechnol
, vol.11
, pp. 209-214
-
-
Chartrain, M.1
Salmon, P.M.2
Robinson, D.K.3
-
130
-
-
0034503418
-
Directed evolution of toluene dioxygense from Pseudomonas putida for improved selectivity toward cis-(1S,2R)-indanediol during indane
-
Zhang N, Stewart BG, Moore IC, et al. Directed evolution of toluene dioxygense from Pseudomonas putida for improved selectivity toward cis-(1S,2R)-indanediol during indane. Metab Eng 2000;2(4):339-48
-
(2000)
Metab Eng
, vol.2
, Issue.4
, pp. 339-348
-
-
Zhang, N.1
Stewart, B.G.2
Moore, I.C.3
-
131
-
-
0346036070
-
Measurement of strain-dependent toxicity in the indene bioconversion using multiparameter flow cytometry
-
Amanullah A, Hewitt CJ, Nienow AW, et al. Measurement of strain-dependent toxicity in the indene bioconversion using multiparameter flow cytometry. Biotechnol Bioeng 2003;81(4):405-20
-
(2003)
Biotechnol Bioeng
, vol.81
, Issue.4
, pp. 405-420
-
-
Amanullah, A.1
Hewitt, C.J.2
Nienow, A.W.3
-
132
-
-
0025641047
-
Potassium channel openers and vascular smooth muscle relaxation
-
Edwards G, Weston AH. Potassium channel openers and vascular smooth muscle relaxation. Pharmacol Ther 1990;48(2):237-58
-
(1990)
Pharmacol Ther
, vol.48
, Issue.2
, pp. 237-258
-
-
Edwards, G.1
Weston, A.H.2
-
133
-
-
0001777548
-
Potassium channel openers: New biological probes
-
Robertson DW, Steinberg MI. Potassium channel openers: new biological probes. Annu Rep Med Chem 1989;24:91-100
-
(1989)
Annu Rep Med Chem
, vol.24
, pp. 91-100
-
-
Robertson, D.W.1
Steinberg, M.I.2
-
134
-
-
0024534172
-
Cromakalim, nicorandil and pinacidil: Novel drugs which open potassium channels in smooth muscle
-
Hamilton TC, Weston AH. Cromakalim, nicorandil and pinacidil: novel drugs which open potassium channels in smooth muscle. Gen Pharmacol 1989;20(1):1-9
-
(1989)
Gen Pharmacol
, vol.20
, Issue.1
, pp. 1-9
-
-
Hamilton, T.C.1
Weston, A.H.2
-
135
-
-
0023030013
-
Synthesis and antihypertensive activity of 4-(cyclic amido)-2H-1-benzopyrans
-
Ashwood VA, Buckingham RE, Cassidy F, et al. Synthesis and antihypertensive activity of 4-(cyclic amido)-2H-1-benzopyrans. J Med Chem 1986;29(11):2194-201
-
(1986)
J Med Chem
, vol.29
, Issue.11
, pp. 2194-2201
-
-
Ashwood, V.A.1
Buckingham, R.E.2
Cassidy, F.3
-
136
-
-
0028458151
-
Stereoselective epoxidation of 2,2-dimethyl-2H-1-benzopyran-6-carbonitrile
-
Patel RN, Banerjee A, Davis B, et al. Stereoselective epoxidation of 2,2-dimethyl-2H-1-benzopyran-6-carbonitrile. Bioorg Med Chem 1994;2(6):535-42
-
(1994)
Bioorg Med Chem
, vol.2
, Issue.6
, pp. 535-542
-
-
Patel, R.N.1
Banerjee, A.2
Davis, B.3
-
137
-
-
0026078484
-
Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase and human DNA polymerases α, β, and γ by the 5′-triphosphates of carbovir, 3′-azido-3′-deoxythymidine, 2′,3′-dideoxyguanosine, and 3′-deoxythymidine. A novel RNA template for the evaluation of antiretroviral drugs
-
Parker WB, White EC, Shaddix SC, et al. Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase and human DNA polymerases α, β, and γ by the 5′-triphosphates of carbovir, 3′-azido-3′-deoxythymidine, 2′,3′-dideoxyguanosine, and 3′-deoxythymidine. A novel RNA template for the evaluation of antiretroviral drugs. J Biol Chem 1991;266(3):1754-62
-
(1991)
J Biol Chem
, vol.266
, Issue.3
, pp. 1754-1762
-
-
Parker, W.B.1
White, E.C.2
Shaddix, S.C.3
-
138
-
-
20444488179
-
-
Muenzer DF, Meinhold P, Peters MW, et al. Stereoselective hydroxylation of an achiral cyclopentanecarboxylic acid derivative using engineered P450s BM-3. Chem Commun (Cambridge, United Kingdom) 2005;20:2597-9
-
Muenzer DF, Meinhold P, Peters MW, et al. Stereoselective hydroxylation of an achiral cyclopentanecarboxylic acid derivative using engineered P450s BM-3. Chem Commun (Cambridge, United Kingdom) 2005;20:2597-9
-
-
-
-
139
-
-
0030063747
-
Microbial hydroxylation of 2-cycloalkylbenzoxazoles. Part III. Determination of product enantiomeric excess and cleavage of benzoxazoles
-
de Raadt A, Griengl H, Petsch M, et al. Microbial hydroxylation of 2-cycloalkylbenzoxazoles. Part III. Determination of product enantiomeric excess and cleavage of benzoxazoles. Tetrahedron:Asymmetry 1996;7(2):491-6
-
(1996)
Tetrahedron:Asymmetry
, vol.7
, Issue.2
, pp. 491-496
-
-
de Raadt, A.1
Griengl, H.2
Petsch, M.3
-
141
-
-
0035830723
-
Rational evolution of a medium chain-specific cytochrome P-450 BM-3 variant
-
Li Q-S, Schwaneberg U, Fischer M, et al. Rational evolution of a medium chain-specific cytochrome P-450 BM-3 variant. Biochim Biophys Acta 2001;1545(1-2):114-21
-
(2001)
Biochim Biophys Acta
, vol.1545
, Issue.1-2
, pp. 114-121
-
-
Li, Q.-S.1
Schwaneberg, U.2
Fischer, M.3
-
142
-
-
39649098137
-
-
Arnold FH, Otey CR. Libraries of optimized cytochrome P450 enzymes and the optimized P450 enzymes exhibiting higher activities and new substrate specificities. WO2005017106 (2005)
-
Arnold FH, Otey CR. Libraries of optimized cytochrome P450 enzymes and the optimized P450 enzymes exhibiting higher activities and new substrate specificities. WO2005017106 (2005)
-
-
-
-
143
-
-
0142164488
-
Myxobacteria: Proficient producers of novel natural products with various biological activities-past and future biotechnological aspects with the focus on the genus Sorangium
-
Gerth K, Pradella S, Perlova O, et al. Myxobacteria: proficient producers of novel natural products with various biological activities-past and future biotechnological aspects with the focus on the genus Sorangium. J Biotechnol 2003; 106(2-3)233-53
-
(2003)
J Biotechnol
, vol.106
, Issue.2-3
, pp. 233-253
-
-
Gerth, K.1
Pradella, S.2
Perlova, O.3
-
144
-
-
39649104699
-
-
Benigni D, Stankavage R, Chiang S-J, et al. Methods for the preparation, isolation and purification of epothilone B, and X-ray crystal structures of epothilone B. WO2004026254 (2004)
-
Benigni D, Stankavage R, Chiang S-J, et al. Methods for the preparation, isolation and purification of epothilone B, and X-ray crystal structures of epothilone B. WO2004026254 (2004)
-
-
-
-
145
-
-
3042701597
-
Epothilones: Mechanism of action and biologic activity
-
Goodin S, Kane MP, Robin EH. Epothilones: mechanism of action and biologic activity. J Clin Oncol 2004;22(1):2015-25
-
(2004)
J Clin Oncol
, vol.22
, Issue.1
, pp. 2015-2025
-
-
Goodin, S.1
Kane, M.P.2
Robin, E.H.3
-
147
-
-
4344607834
-
The merger of natural product synthesis and medicinal chemistry: On the chemistry and chemical biology of epothilones
-
Altmann K-H. The merger of natural product synthesis and medicinal chemistry: on the chemistry and chemical biology of epothilones. Org Biomol Chem 2004;2(15):2137-52
-
(2004)
Org Biomol Chem
, vol.2
, Issue.15
, pp. 2137-2152
-
-
Altmann, K.-H.1
-
148
-
-
2942635105
-
Precursor-directed biosynthesis of epothilone in Escherichia coli
-
Boddy CN, Hotta K, Tse ML, et al. Precursor-directed biosynthesis of epothilone in Escherichia coli. J Am Chem Soc 2004;126(24):7436-7
-
(2004)
J Am Chem Soc
, vol.126
, Issue.24
, pp. 7436-7437
-
-
Boddy, C.N.1
Hotta, K.2
Tse, M.L.3
-
150
-
-
33846417686
-
Cloning and expression of acytochrome P450 hydroxylase gene from Amycolatopsis orientalis: Hydroxylation of epothilone B for the production of epothilone F
-
Basch J, Chiang S-H. Cloning and expression of acytochrome P450 hydroxylase gene from Amycolatopsis orientalis: hydroxylation of epothilone B for the production of epothilone F. J Ind Microbiol Biotechnol 2007;34(2):171-6
-
(2007)
J Ind Microbiol Biotechnol
, vol.34
, Issue.2
, pp. 171-176
-
-
Basch, J.1
Chiang, S.-H.2
-
151
-
-
11344268494
-
BMS-310705 Bristol-Myers Squibb/GBF
-
Kolman A. BMS-310705 Bristol-Myers Squibb/GBF. Curr Opin Investig Drugs 2004;5(12):1292-7
-
(2004)
Curr Opin Investig Drugs
, vol.5
, Issue.12
, pp. 1292-1297
-
-
Kolman, A.1
-
152
-
-
0001417898
-
Mechanism of action of antibacterial agents. Tiamulin and pleuromutilin
-
Hoegenauer G. Mechanism of action of antibacterial agents. Tiamulin and pleuromutilin. Antibiotics (New York) 1979;5(1):344-60
-
(1979)
Antibiotics (New York)
, vol.5
, Issue.1
, pp. 344-360
-
-
Hoegenauer, G.1
-
153
-
-
0009528835
-
Chemistry of pleuromutilins. V. Photoisomerization of AB-trans-anellated mutilan-11-one
-
Berner H, Vyplel H, Schulz C, et al. Chemistry of pleuromutilins. V. Photoisomerization of AB-trans-anellated mutilan-11-one. Tetrahedron 1983;39(10):1745-8
-
(1983)
Tetrahedron
, vol.39
, Issue.10
, pp. 1745-1748
-
-
Berner, H.1
Vyplel, H.2
Schulz, C.3
-
154
-
-
0036322329
-
Hydroxylation of mutilin by Streptomyces griseus and Cunninghamella echinulata
-
Hanson RL, Matson JA, Brzozowski DB, et al. Hydroxylation of mutilin by Streptomyces griseus and Cunninghamella echinulata. Org Proc Res Dev 2002;6(4):482-7
-
(2002)
Org Proc Res Dev
, vol.6
, Issue.4
, pp. 482-487
-
-
Hanson, R.L.1
Matson, J.A.2
Brzozowski, D.B.3
-
155
-
-
0038363790
-
Synthesis and activity of a C-8 keto pleuromutilin derivative
-
Springer DM, Sorenson ME, Huang S, et al. Synthesis and activity of a C-8 keto pleuromutilin derivative. Bioorg Med Chem Lett 2003;13(10):1751-3
-
(2003)
Bioorg Med Chem Lett
, vol.13
, Issue.10
, pp. 1751-1753
-
-
Springer, D.M.1
Sorenson, M.E.2
Huang, S.3
-
156
-
-
79953270102
-
-
Janssen DB. Dehalogenases in biodegradation and biocatalysis. In: Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 441-62
-
Janssen DB. Dehalogenases in biodegradation and biocatalysis. In: Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 441-62
-
-
-
-
157
-
-
0031716312
-
Optically active chlorohydrins as chiral C3 and C4 building units: Microbial resolution and synthetic applications
-
Kasai N, Suzuki T, Furukawa Y. Optically active chlorohydrins as chiral C3 and C4 building units: microbial resolution and synthetic applications. Chirality 1998;1097:682-92
-
(1998)
Chirality
, vol.1097
, pp. 682-692
-
-
Kasai, N.1
Suzuki, T.2
Furukawa, Y.3
-
158
-
-
0242438879
-
Industrialization of the microbial resolution of chiral C3 and C4 synthetic units: From a small beginning to a major operation, a personal account
-
Kasai N, Suzuki T. Industrialization of the microbial resolution of chiral C3 and C4 synthetic units: from a small beginning to a major operation, a personal account. Adv Synthesis Catalysis 2003;345(4):437-55
-
(2003)
Adv Synthesis Catalysis
, vol.345
, Issue.4
, pp. 437-455
-
-
Kasai, N.1
Suzuki, T.2
-
159
-
-
0025744330
-
A novel method for the generation of (R)- and (S)-3-chloro-1,2-propanediol by stereospecific dehalogenating bacteria and their use in the preparation of (R)- and (S)-glycidol
-
Suzuki T, Kasai N. A novel method for the generation of (R)- and (S)-3-chloro-1,2-propanediol by stereospecific dehalogenating bacteria and their use in the preparation of (R)- and (S)-glycidol. Bioorg Med Chem Lett 1991;1(7):343-6
-
(1991)
Bioorg Med Chem Lett
, vol.1
, Issue.7
, pp. 343-346
-
-
Suzuki, T.1
Kasai, N.2
-
160
-
-
0030575817
-
A novel generation of optically active ethyl 4-chloro-3-hydroxybutyrate as a C4 chiral building unit using microbial dechlorination
-
Suzuki T, Idogaki H, Kasai N. A novel generation of optically active ethyl 4-chloro-3-hydroxybutyrate as a C4 chiral building unit using microbial dechlorination. Tetrahedron:Asymmetry 1996;7(11):3109-12
-
(1996)
Tetrahedron:Asymmetry
, vol.7
, Issue.11
, pp. 3109-3112
-
-
Suzuki, T.1
Idogaki, H.2
Kasai, N.3
-
161
-
-
17844391799
-
Improved catalytic properties of halohydrin dehalogenase by modification of the halide-binding site
-
Tang L, Pazmino DET, Fraaije MW, et al. Improved catalytic properties of halohydrin dehalogenase by modification of the halide-binding site. Biochemistry 2005;44(17):6609-18
-
(2005)
Biochemistry
, vol.44
, Issue.17
, pp. 6609-6618
-
-
Tang, L.1
Pazmino, D.E.T.2
Fraaije, M.W.3
-
162
-
-
0037074924
-
Improved stability of halohydrin dehalogenase from Agrobacterium radiobacter AD1 by replacement of cysteine residues
-
Tang L, van Hylckama Vlieg JET, et al. Improved stability of halohydrin dehalogenase from Agrobacterium radiobacter AD1 by replacement of cysteine residues. Enzyme Microb Technol 2002;30(2):251-8
-
(2002)
Enzyme Microb Technol
, vol.30
, Issue.2
, pp. 251-258
-
-
Tang, L.1
van Hylckama Vlieg, J.E.T.2
-
163
-
-
0025998074
-
A new catalytic function of halohydrin hydrogen-halide-lyase, synthesis of β-hydroxynitriles from epoxides and cyanide
-
Nakamura T, Nagasawa T, Yu F, et al. A new catalytic function of halohydrin hydrogen-halide-lyase, synthesis of β-hydroxynitriles from epoxides and cyanide. Biochem Biophys Res Commun 1991;180(1):124-30
-
(1991)
Biochem Biophys Res Commun
, vol.180
, Issue.1
, pp. 124-130
-
-
Nakamura, T.1
Nagasawa, T.2
Yu, F.3
-
164
-
-
0037054398
-
Exploration of the biocatalytic potential of a halohydrin dehalogenase using chromogenic substrates
-
Lutje Spelberg JHL, Tang L, van Gelder M, et al. Exploration of the biocatalytic potential of a halohydrin dehalogenase using chromogenic substrates. Tetrahedron:Asymmetry 2002;13(10):1083-9
-
(2002)
Tetrahedron:Asymmetry
, vol.13
, Issue.10
, pp. 1083-1089
-
-
Lutje Spelberg, J.H.L.1
Tang, L.2
van Gelder, M.3
-
165
-
-
0042367657
-
Highly enantioselective and regioselective biocatalytic azidolysis of aromatic epoxides
-
Lutje Spelberg JH, van Hylckama Vlieg JET, Tang L, et al. Highly enantioselective and regioselective biocatalytic azidolysis of aromatic epoxides. Org Lett 2001;3(1):41-3
-
(2001)
Org Lett
, vol.3
, Issue.1
, pp. 41-43
-
-
Lutje Spelberg, J.H.1
van Hylckama Vlieg, J.E.T.2
Tang, L.3
-
166
-
-
1642587823
-
-
Lutje Spelberg JH, Tang L, Kellogg RM, et al. Enzymatic dynamic kinetic resolution of epihalohydrins. Tetrahedron: Asymmetry2004;15(7):1095-2
-
Lutje Spelberg JH, Tang L, Kellogg RM, et al. Enzymatic dynamic kinetic resolution of epihalohydrins. Tetrahedron: Asymmetry2004;15(7):1095-2
-
-
-
-
167
-
-
17844364193
-
Nitrite-mediated hydrolysis of epoxides catalyzed by halohydrin dehalogenase from Agrobacterium radiobacter AD1: A new tool for the kinetic resolution of epoxides
-
Hasnaoui G, Lutje Spelberg JH, de Vries E, et al. Nitrite-mediated hydrolysis of epoxides catalyzed by halohydrin dehalogenase from Agrobacterium radiobacter AD1: a new tool for the kinetic resolution of epoxides. Tetrahedron: Asymmetry 2005;16(9):1685-92
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, Issue.9
, pp. 1685-1692
-
-
Hasnaoui, G.1
Lutje Spelberg, J.H.2
de Vries, E.3
-
168
-
-
33645936298
-
-
Elenkov MM, Hauer B, Janssen DB. Enantioselective ring opening of epoxides with cyanide catalyzed by halohydrin dehalogenases: a new approach to nonracemic β-hydroxy nitriles. Adv Synthesis Catalysis 2006; 348(4+5):579-85
-
Elenkov MM, Hauer B, Janssen DB. Enantioselective ring opening of epoxides with cyanide catalyzed by halohydrin dehalogenases: a new approach to nonracemic β-hydroxy nitriles. Adv Synthesis Catalysis 2006; 348(4+5):579-85
-
-
-
-
169
-
-
15444362586
-
Enzyme-catalyzed aldol additions
-
Fessner W-D. Enzyme-catalyzed aldol additions. Mod Aldol React 2004; 1:201-72
-
(2004)
Mod Aldol React
, vol.1
, pp. 201-272
-
-
Fessner, W.-D.1
-
170
-
-
0034213036
-
The synthesis of chiral cyanohydrins by oxynitrilases
-
Griengl H, Schwab H, Fechter M. The synthesis of chiral cyanohydrins by oxynitrilases. Trends Biotechnol 2000;18(6):252-6
-
(2000)
Trends Biotechnol
, vol.18
, Issue.6
, pp. 252-256
-
-
Griengl, H.1
Schwab, H.2
Fechter, M.3
-
171
-
-
0042628455
-
Thiamin-diphosphate-dependent enzymes: New aspects of asymmetric C-C bond formation
-
Pohl M, Lingen B, Muller M. Thiamin-diphosphate-dependent enzymes: new aspects of asymmetric C-C bond formation. Chem A Eur J 2002;8(23):5288-95
-
(2002)
Chem A Eur J
, vol.8
, Issue.23
, pp. 5288-5295
-
-
Pohl, M.1
Lingen, B.2
Muller, M.3
-
172
-
-
0035709383
-
Biocatalytic synthesis of hydroxylated natural products using aldolases and related enzymes
-
Fessner W-D, Helaine V. Biocatalytic synthesis of hydroxylated natural products using aldolases and related enzymes. Curr Opin Biotechnol 2001;12(6):574-86
-
(2001)
Curr Opin Biotechnol
, vol.12
, Issue.6
, pp. 574-586
-
-
Fessner, W.-D.1
Helaine, V.2
-
173
-
-
0033545539
-
Synthetic potential of thiamin diphosphate-dependent enzymes
-
Sprenger GA, Pohl M. Synthetic potential of thiamin diphosphate-dependent enzymes. J Mol Catalysis B Enzymatic 1999;6(3):145-59
-
(1999)
J Mol Catalysis B Enzymatic
, vol.6
, Issue.3
, pp. 145-159
-
-
Sprenger, G.A.1
Pohl, M.2
-
175
-
-
4243614209
-
Enzyme-mediated decarboxylase reactions in organic synthesis
-
Patel RN, editor, Marcel Dekker, NY
-
Ohta H, Sugai T. Enzyme-mediated decarboxylase reactions in organic synthesis. In: Stereoselective Biocatalysis. Patel RN, editor, Marcel Dekker, NY. 2000. p. 487-526
-
(2000)
Stereoselective Biocatalysis
, pp. 487-526
-
-
Ohta, H.1
Sugai, T.2
-
176
-
-
0032472314
-
Industrial biotransformations for the production of D-amino acids
-
Yagasaki M, Ozaki A. Industrial biotransformations for the production of D-amino acids. J Mol Catalysis B Enzymatic 1998;4(1-2):1-11
-
(1998)
J Mol Catalysis B Enzymatic
, vol.4
, Issue.1-2
, pp. 1-11
-
-
Yagasaki, M.1
Ozaki, A.2
-
177
-
-
0010466583
-
Enantiospecific production of (S)-2-hydroxypropiophenone mediated by benzoylformate decarboxylase from Acinetobacter calcoaceticus
-
Prosen E, Ward OP, Collins S, et al. Enantiospecific production of (S)-2-hydroxypropiophenone mediated by benzoylformate decarboxylase from Acinetobacter calcoaceticus. Biocatalysis 1993;8(1):21-9
-
(1993)
Biocatalysis
, vol.8
, Issue.1
, pp. 21-29
-
-
Prosen, E.1
Ward, O.P.2
Collins, S.3
-
178
-
-
0343775587
-
Asymmetric benzoin reaction catalyzed by benzoylformate decarboxylase
-
Demir AS, Dunnwald T, Iding H, et al. Asymmetric benzoin reaction catalyzed by benzoylformate decarboxylase. Tetrahedron:Asymmetry 1999;10(24):4769-74
-
(1999)
Tetrahedron:Asymmetry
, vol.10
, Issue.24
, pp. 4769-4774
-
-
Demir, A.S.1
Dunnwald, T.2
Iding, H.3
-
179
-
-
39649112971
-
-
Patel RN, editor, CRC Press, FL
-
Pohl M, Liese A. Industrial processes using lyases for C-C, C-N, and C-C bond formation. Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 661-76
-
(2007)
Industrial processes using lyases for C-C, C-N, and C-C bond formation. Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 661-676
-
-
Pohl, M.1
Liese, A.2
-
180
-
-
0033381135
-
Asymmetric acyloin condensation catalyzed by phenylpyruvate decarboxylase
-
Guo Z, Goswami A, Mirfakhrae KD, et al. Asymmetric acyloin condensation catalyzed by phenylpyruvate decarboxylase. Tetrahedron:Asymmetry 1999; 10(24):4667-75
-
(1999)
Tetrahedron:Asymmetry
, vol.10
, Issue.24
, pp. 4667-4675
-
-
Guo, Z.1
Goswami, A.2
Mirfakhrae, K.D.3
-
181
-
-
0033180036
-
Development of an enzymatic system for the production of dopamine from catechol, pyruvate and ammonia
-
Lee S-G, Hong S-P, Sung M-H. Development of an enzymatic system for the production of dopamine from catechol, pyruvate and ammonia. Enzyme Microb Technol1999;25:298-302
-
Enzyme Microb Technol1999;25
, pp. 298-302
-
-
Lee, S.-G.1
Hong, S.-P.2
Sung, M.-H.3
-
182
-
-
0032357832
-
Production of L-lactic acid and L-malic acid by intact and immobilized cells of Lactobacillus casei
-
Abelyan VA, Abelyan LA. Production of L-lactic acid and L-malic acid by intact and immobilized cells of Lactobacillus casei. Appl Biochem Microbiol 1998;34:578-80
-
(1998)
Appl Biochem Microbiol
, vol.34
, pp. 578-580
-
-
Abelyan, V.A.1
Abelyan, L.A.2
-
183
-
-
0026692637
-
Acyloin formation by benzoylformate decarboxylase from Pseudomonas putida
-
Wilcocks R, Ward OP, Collins S, et al. Acyloin formation by benzoylformate decarboxylase from Pseudomonas putida. Appl Environ Microbiol 1992; 5895:1699-704
-
(1992)
Appl Environ Microbiol
, vol.5895
, pp. 1699-1704
-
-
Wilcocks, R.1
Ward, O.P.2
Collins, S.3
-
184
-
-
39649098799
-
Enantioselective syntheses of hydtoxy ketones via benzoylformate decarboxylase- and benzaldehyde lyase-catalyzed C-C bond formation
-
Lingen B, Pohl M, Demir AS, et al. Enantioselective syntheses of hydtoxy ketones via benzoylformate decarboxylase- and benzaldehyde lyase-catalyzed C-C bond formation. Oxidative Stress Dis 2004;11:113-29
-
(2004)
Oxidative Stress Dis
, vol.11
, pp. 113-129
-
-
Lingen, B.1
Pohl, M.2
Demir, A.S.3
-
185
-
-
0036656222
-
Improving the carboligase activity of benzoylformate decarboxylase from Pseudomonas putida by a combination of directed evolution and site-directed mutagenesis
-
Lingen B, Groetzinger J, Kolter D, et al. Improving the carboligase activity of benzoylformate decarboxylase from Pseudomonas putida by a combination of directed evolution and site-directed mutagenesis. Protein Eng 2002; 15(7):585-93
-
(2002)
Protein Eng
, vol.15
, Issue.7
, pp. 585-593
-
-
Lingen, B.1
Groetzinger, J.2
Kolter, D.3
-
186
-
-
34547178959
-
-
Dean SM, Greenberg WA, Wong C-H. Recent advances in aldolase-catalyzed asymmetric synthesis. Adv Synthesis Catalysis 2007;349(8+9):1308-20
-
Dean SM, Greenberg WA, Wong C-H. Recent advances in aldolase-catalyzed asymmetric synthesis. Adv Synthesis Catalysis 2007;349(8+9):1308-20
-
-
-
-
187
-
-
1542763243
-
Enzyme-catalyzed organic synthesis: Practical routes to aza sugars and their analogs for use as glycoprocessing inhibitors
-
Look GC, Gary C, Fotsch CH, et al. Enzyme-catalyzed organic synthesis: practical routes to aza sugars and their analogs for use as glycoprocessing inhibitors. Acc Chem Res 1993;26:282-90
-
(1993)
Acc Chem Res
, vol.26
, pp. 282-290
-
-
Look, G.C.1
Gary, C.2
Fotsch, C.H.3
-
188
-
-
0000535157
-
Palladium-mediated stereocontrolled reductive amination of azido sugars prepared from enzymic aldol condensation: A general approach to the synthesis of deoxy az94a sugars
-
Kajimoto T, Chen L, Liu KKC, Wong C-H. Palladium-mediated stereocontrolled reductive amination of azido sugars prepared from enzymic aldol condensation: a general approach to the synthesis of deoxy az94a sugars. J Am Chem Soc 1991; 113(17):6678-80
-
(1991)
J Am Chem Soc
, vol.113
, Issue.17
, pp. 6678-6680
-
-
Kajimoto, T.1
Chen, L.2
Liu, K.K.C.3
Wong, C.-H.4
-
189
-
-
0000919179
-
Enzyme-catalyzed reactions. 3. Enzyme-catalyzed synthesis of deoxymannojirimycin, 1-deoxynojirimycin and 1,4-dideoxy-1,4-imino-D-arabinitol
-
Ziegler T, Straub OA, Effenberger F. Enzyme-catalyzed reactions. 3. Enzyme-catalyzed synthesis of deoxymannojirimycin, 1-deoxynojirimycin and 1,4-dideoxy-1,4-imino-D-arabinitol. Angew Chem 1988;100(5):737-38
-
(1988)
Angew Chem
, vol.100
, Issue.5
, pp. 737-738
-
-
Ziegler, T.1
Straub, O.A.2
Effenberger, F.3
-
190
-
-
0001765832
-
Enzyme-catalyzed aldol condensation for asymmetric synthesis of azasugars: Synthesis, evaluation, and modeling of glycosidase inhibitors
-
Kajimoto T, Liu KKC, Pederson RL, et al. Enzyme-catalyzed aldol condensation for asymmetric synthesis of azasugars: synthesis, evaluation, and modeling of glycosidase inhibitors. J Am Chem Soc 1991; 113(16):6187-96
-
(1991)
J Am Chem Soc
, vol.113
, Issue.16
, pp. 6187-6196
-
-
Kajimoto, T.1
Liu, K.K.C.2
Pederson, R.L.3
-
191
-
-
0034549491
-
Chemo-enzymatic total synthesis of 3-epiaustraline, australine, and 7-epialexine
-
Romero A, Wong C-H. Chemo-enzymatic total synthesis of 3-epiaustraline, australine, and 7-epialexine. J Org Chem 2000;65(24):8264-8
-
(2000)
J Org Chem
, vol.65
, Issue.24
, pp. 8264-8268
-
-
Romero, A.1
Wong, C.-H.2
-
192
-
-
0030657459
-
Stereospecific preparation of the N-terminal amino acid moiety of Nikkomycins KX and KZ via a multiple enzyme synthesis
-
Henderson DP, Shelton MC, Cotterill IC, et al. Stereospecific preparation of the N-terminal amino acid moiety of Nikkomycins KX and KZ via a multiple enzyme synthesis. J Org Chem 1997;62(23):7910-11
-
(1997)
J Org Chem
, vol.62
, Issue.23
, pp. 7910-7911
-
-
Henderson, D.P.1
Shelton, M.C.2
Cotterill, I.C.3
-
193
-
-
0028933270
-
CMP-KDO synthetase: Overproduction and application to the synthesis of CMP-KDO and analogs
-
Sugai T, Lin CH, Shin GJ, et al. CMP-KDO synthetase: overproduction and application to the synthesis of CMP-KDO and analogs. Bioorg Med Chem 1995;3(3):313-20
-
(1995)
Bioorg Med Chem
, vol.3
, Issue.3
, pp. 313-320
-
-
Sugai, T.1
Lin, C.H.2
Shin, G.J.3
-
194
-
-
0030293657
-
Characterization of the chemoenzymic synthesis of N-acetyl-D-neuraminic acid (Neu5Ac)
-
Blayer S, Woodley JM, Lilly MD, et al. Characterization of the chemoenzymic synthesis of N-acetyl-D-neuraminic acid (Neu5Ac). Biotechnol Prog 1996;12(6):758-63
-
(1996)
Biotechnol Prog
, vol.12
, Issue.6
, pp. 758-763
-
-
Blayer, S.1
Woodley, J.M.2
Lilly, M.D.3
-
195
-
-
0031127901
-
An efficient process for production of N-acetylneuraminic acid using N-acetylneuraminic acid aldolase
-
Mahmoudian M, Noble D, Drake CS, et al. An efficient process for production of N-acetylneuraminic acid using N-acetylneuraminic acid aldolase. Enzyme Microbial Technol 1997; 20(5):393-400
-
(1997)
Enzyme Microbial Technol
, vol.20
, Issue.5
, pp. 393-400
-
-
Mahmoudian, M.1
Noble, D.2
Drake, C.S.3
-
196
-
-
0039478543
-
Enzymatic, two-step synthesis of N-acetylneuraminic acid in a enzyme-membrane reactor
-
Kragl U, Gygax D, Ghisalba O, et al. Enzymatic, two-step synthesis of N-acetylneuraminic acid in a enzyme-membrane reactor. Angew Chem 1991;103(7):854-5
-
(1991)
Angew Chem
, vol.103
, Issue.7
, pp. 854-855
-
-
Kragl, U.1
Gygax, D.2
Ghisalba, O.3
-
197
-
-
0028854636
-
Sequential three- and four-substrate aldol reactions catalyzed by aldolases
-
Gijsen HJM, Wong C-H. Sequential three- and four-substrate aldol reactions catalyzed by aldolases. J Am Chem Soc 1995;117(29):7585-91
-
(1995)
J Am Chem Soc
, vol.117
, Issue.29
, pp. 7585-7591
-
-
Gijsen, H.J.M.1
Wong, C.-H.2
-
198
-
-
1942469509
-
Development of an efficient, scalable, aldolase-catalyzed process for enantioselective synthesis of statin intermediates
-
Greenberg WA, Varvak A, Hanson SR et al. Development of an efficient, scalable, aldolase-catalyzed process for enantioselective synthesis of statin intermediates. Proc Natl Acad Sci USA 2004;101(16):5788-93
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, Issue.16
, pp. 5788-5793
-
-
Greenberg, W.A.1
Varvak, A.2
Hanson, S.R.3
-
199
-
-
0033369951
-
Neuropeptides and capsaicin stimulate the release of inflammatory cytokines in a human bronchial epithelial cell line
-
Veronesi B, Carter JD, Devlin RB, et al. Neuropeptides and capsaicin stimulate the release of inflammatory cytokines in a human bronchial epithelial cell line. Neuropeptides (Edinburgh) 1999;33(6):447-56
-
(1999)
Neuropeptides (Edinburgh)
, vol.33
, Issue.6
, pp. 447-456
-
-
Veronesi, B.1
Carter, J.D.2
Devlin, R.B.3
-
200
-
-
0032004070
-
Characterization of tachykinin receptors mediating bronchomotor and vasodepressor responses to neuropeptide γ and substance P in the anesthetized rabbit
-
Yuan L, Burcher E, Nail BS. Characterization of tachykinin receptors mediating bronchomotor and vasodepressor responses to neuropeptide γ and substance P in the anesthetized rabbit. Pulm Pharmacol Ther 1998; 11(1):31-9
-
(1998)
Pulm Pharmacol Ther
, vol.11
, Issue.1
, pp. 31-39
-
-
Yuan, L.1
Burcher, E.2
Nail, B.S.3
-
201
-
-
0034675392
-
Synthesis and NK1/NK2 receptor activity of substituted 4(Z)-(methoxyimino) pentyl-1-piperazines
-
Ting PC, Lee JF, Anthes JC, et al. Synthesis and NK1/NK2 receptor activity of substituted 4(Z)-(methoxyimino) pentyl-1-piperazines. Bioorg Med Chem Lett 2000;10(20):2333-5
-
(2000)
Bioorg Med Chem Lett
, vol.10
, Issue.20
, pp. 2333-2335
-
-
Ting, P.C.1
Lee, J.F.2
Anthes, J.C.3
-
202
-
-
0034675695
-
The design and synthesis of novel NK1/NK2 dual antagonists
-
Reichard GA, Ball ZT, Aslanian R, et al. The design and synthesis of novel NK1/NK2 dual antagonists. Bioorg Med Chem Lett 2000; 10(20):2329-32
-
(2000)
Bioorg Med Chem Lett
, vol.10
, Issue.20
, pp. 2329-2332
-
-
Reichard, G.A.1
Ball, Z.T.2
Aslanian, R.3
-
203
-
-
0013170373
-
Enzymatic hydrolysis of a prochiral 3-substituted glutarate ester, an intermediate in the synthesis of an NK1/NK2 dual antagonist
-
Homann MJ, Vail R, Morgan B, et al. Enzymatic hydrolysis of a prochiral 3-substituted glutarate ester, an intermediate in the synthesis of an NK1/NK2 dual antagonist. Adv Synthesis Catalysis 2001;343(6-7):744-9
-
(2001)
Adv Synthesis Catalysis
, vol.343
, Issue.6-7
, pp. 744-749
-
-
Homann, M.J.1
Vail, R.2
Morgan, B.3
-
204
-
-
1842765645
-
Improved activity and thermostability of Candida antarctica lipase B by DNA family shuffling
-
Suen W-C, Zhang N, Xiao L, et al. Improved activity and thermostability of Candida antarctica lipase B by DNA family shuffling. Protein Eng Design Sel 2004;17(2):133-40
-
(2004)
Protein Eng Design Sel
, vol.17
, Issue.2
, pp. 133-140
-
-
Suen, W.-C.1
Zhang, N.2
Xiao, L.3
-
205
-
-
0141817121
-
Improving tolerance of Candida Antarctica lipase B towards irreversible thermal inactivation through directed evolution
-
Zhang N, Suen W-C, Windsor W, et al. Improving tolerance of Candida Antarctica lipase B towards irreversible thermal inactivation through directed evolution. Protein Eng 2003;16(8):599-605
-
(2003)
Protein Eng
, vol.16
, Issue.8
, pp. 599-605
-
-
Zhang, N.1
Suen, W.-C.2
Windsor, W.3
-
206
-
-
0141645603
-
Creation of a productive, highly enantioselective nitrilase through gene site saturation mutagenesis (GSSM)
-
DeSantis G, Wong K, Farwell B, et al. Creation of a productive, highly enantioselective nitrilase through gene site saturation mutagenesis (GSSM). J Am Chem Soc 2003;125(38):11476-7
-
(2003)
J Am Chem Soc
, vol.125
, Issue.38
, pp. 11476-11477
-
-
DeSantis, G.1
Wong, K.2
Farwell, B.3
-
207
-
-
0037036726
-
An enzyme library approach to biocatalysis: Development of nitrilases for enantioselective production of carboxylic acid derivatives
-
DeSantis C, Zhu Z, Greenberg WA, et al. An enzyme library approach to biocatalysis: development of nitrilases for enantioselective production of carboxylic acid derivatives. J Am Chem Soc 2002;124(31):9024-5
-
(2002)
J Am Chem Soc
, vol.124
, Issue.31
, pp. 9024-9025
-
-
DeSantis, C.1
Zhu, Z.2
Greenberg, W.A.3
-
208
-
-
39649122003
-
-
Desantis G, Short JM, Burk M, et al. Identification, cloning, sequences and design of nitrilases for synthesis of enantioselective amino acids and hydroxy acids. WO2003097810 (2003)
-
Desantis G, Short JM, Burk M, et al. Identification, cloning, sequences and design of nitrilases for synthesis of enantioselective amino acids and hydroxy acids. WO2003097810 (2003)
-
-
-
-
209
-
-
4344663593
-
Exploring nitrilase sequence space for enantioselective catalysis
-
Robertson DE, Chaplin JA, DeSantis G, et al. Exploring nitrilase sequence space for enantioselective catalysis. Appl Environ Microbiol 2004;70(4):2429-36
-
(2004)
Appl Environ Microbiol
, vol.70
, Issue.4
, pp. 2429-2436
-
-
Robertson, D.E.1
Chaplin, J.A.2
DeSantis, G.3
-
210
-
-
0026675653
-
Disodium (R,R)5-[2-(3-chlorophenyl)-2 hydroxyethyl]amino]propyl]-1,3-benzodioxole-2,2 dicarboxylate. A potent adrenergic agonist virtually specific for 3 receptors
-
Bloom JD, Datta MD, Johnson BD, et al. Disodium (R,R)5-[2-(3-chlorophenyl)-2 hydroxyethyl]amino]propyl]-1,3-benzodioxole-2,2 dicarboxylate. A potent adrenergic agonist virtually specific for 3 receptors. J Med Chem 1989;35:3081-4
-
(1989)
J Med Chem
, vol.35
, pp. 3081-3084
-
-
Bloom, J.D.1
Datta, M.D.2
Johnson, B.D.3
-
211
-
-
0030575622
-
BMS-187257, a potent, selective, and novel heterocyclic-3 adrenergic receptor agonist
-
Fisher LG, Sher PM, Skwish S, et al. BMS-187257, a potent, selective, and novel heterocyclic-3 adrenergic receptor agonist. Bioorg Med Chem Lett 1994;6:2253-8
-
(1994)
Bioorg Med Chem Lett
, vol.6
, pp. 2253-2258
-
-
Fisher, L.G.1
Sher, P.M.2
Skwish, S.3
-
212
-
-
0032202392
-
Microbial synthesis of chiral intermediates for 3-receptor agonists
-
Patel RN, Banerjee A, Chu L, et al. Microbial synthesis of chiral intermediates for 3-receptor agonists. J Am Oil Chem Soc 1998;75:1473-82
-
(1998)
J Am Oil Chem Soc
, vol.75
, pp. 1473-1482
-
-
Patel, R.N.1
Banerjee, A.2
Chu, L.3
-
213
-
-
0003160677
-
Semisynthesis of taxol and taxotere
-
Suffness M, editor, CRC Press, NY
-
Holton R, Biediger R, Joatman P. Semisynthesis of taxol and taxotere. In: Taxol: Science and Application. Suffness M, editor, CRC Press, NY. 1995. p. 97-123
-
(1995)
Taxol: Science and Application
, pp. 97-123
-
-
Holton, R.1
Biediger, R.2
Joatman, P.3
-
214
-
-
0032790361
-
A new semisynthesis of paclitaxel from baccatin III
-
Baloglu E, Kingston DG. A new semisynthesis of paclitaxel from baccatin III. J Nat Prod 1999;62(7):1068-71
-
(1999)
J Nat Prod
, vol.62
, Issue.7
, pp. 1068-1071
-
-
Baloglu, E.1
Kingston, D.G.2
-
215
-
-
0028486239
-
Enzymic preparation of (3R-cis)-3-(acetyloxy)-4-phenyl-2-azetidinone: A taxol side-chain synthon
-
Patel RN, Banerjee A, Ko RY, et al. Enzymic preparation of (3R-cis)-3-(acetyloxy)-4-phenyl-2-azetidinone: a taxol side-chain synthon. Biotechnol Appl Biochem 1994;20(1):23-33
-
(1994)
Biotechnol Appl Biochem
, vol.20
, Issue.1
, pp. 23-33
-
-
Patel, R.N.1
Banerjee, A.2
Ko, R.Y.3
-
216
-
-
0034778514
-
Preclinical pharmacology of BMS-275183, an orally active taxane
-
Rose WC, Long BH, Fairchild CR, et al. Preclinical pharmacology of BMS-275183, an orally active taxane. Clin Cancer Res 2001;7(7):2016-21
-
(2001)
Clin Cancer Res
, vol.7
, Issue.7
, pp. 2016-2021
-
-
Rose, W.C.1
Long, B.H.2
Fairchild, C.R.3
-
217
-
-
0345016367
-
Enzymatic preparation of (3R)-cis-3-acetyloxy-4-(1,1-dimethylethyl)-2-azetidinone: A side-chain synthon for an orally active taxane
-
Patel RN, Howell JM, Chidambaram R, et al. Enzymatic preparation of (3R)-cis-3-acetyloxy-4-(1,1-dimethylethyl)-2-azetidinone: a side-chain synthon for an orally active taxane. Tetrahedron: Asymmetry 2003;14(23):3673-7
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, Issue.23
, pp. 3673-3677
-
-
Patel, R.N.1
Howell, J.M.2
Chidambaram, R.3
-
218
-
-
0035313421
-
Synthetic applications of epoxide hydrolases
-
Archelas A, Furstoss R. Synthetic applications of epoxide hydrolases. Curr Opin Chem Biol 2001;5(2):112-9
-
(2001)
Curr Opin Chem Biol
, vol.5
, Issue.2
, pp. 112-119
-
-
Archelas, A.1
Furstoss, R.2
-
219
-
-
0035710814
-
Microbial epoxide hydrolases for preparative biotransformations
-
Steinreiber A, Faber K. Microbial epoxide hydrolases for preparative biotransformations. Curr Opin Biotechnol 2001;12(6):552-8
-
(2001)
Curr Opin Biotechnol
, vol.12
, Issue.6
, pp. 552-558
-
-
Steinreiber, A.1
Faber, K.2
-
220
-
-
0004059155
-
Preparation of benzofuran and dihydrobenzofuran melatonergic agents
-
US5856529
-
Catt JD, Johnson G, Keavy DJ, et al. Preparation of benzofuran and dihydrobenzofuran melatonergic agents. US5856529 (1999)
-
(1999)
-
-
Catt, J.D.1
Johnson, G.2
Keavy, D.J.3
-
221
-
-
0033551906
-
Stereospecific enzymatic hydrolysis of raemic epoxide: A process for making chiral epoxide
-
Goswami A, Totleben MJ, Singh AK, et al. Stereospecific enzymatic hydrolysis of raemic epoxide: a process for making chiral epoxide. Tetrahedron:Asymmetry 1999;10(16):3167-75
-
(1999)
Tetrahedron:Asymmetry
, vol.10
, Issue.16
, pp. 3167-3175
-
-
Goswami, A.1
Totleben, M.J.2
Singh, A.K.3
-
222
-
-
0037019977
-
Phenylhydrazide as an enzyme-labile protecting group in peptide synthesis
-
Voelkert M, Koul S, Mueller GH, et al. Phenylhydrazide as an enzyme-labile protecting group in peptide synthesis. J Org Chem 2002;67(20):6902-10
-
(2002)
J Org Chem
, vol.67
, Issue.20
, pp. 6902-6910
-
-
Voelkert, M.1
Koul, S.2
Mueller, G.H.3
-
224
-
-
0030882113
-
L-methionine related L-amino acids by acylase cleavage of their corresponding N-acetyl-DL-derivatives
-
Bommarius AS, Drauz K, Gunther K, et al. L-methionine related L-amino acids by acylase cleavage of their corresponding N-acetyl-DL-derivatives. Tetrahedron: Asymmetry 1997;8(19):3197-200
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, Issue.19
, pp. 3197-3200
-
-
Bommarius, A.S.1
Drauz, K.2
Gunther, K.3
-
225
-
-
0005214592
-
Stereoselective synthesis using hydantoinases and carbamoylases
-
Patel RN, editor, Marcel Dekker, NY
-
Ogawa J, Shimizu S. Stereoselective synthesis using hydantoinases and carbamoylases. In: Stereoselective Biocatalysis. Patel RN, editor, Marcel Dekker, NY. 2000. p. 1-21
-
(2000)
Stereoselective Biocatalysis
, pp. 1-21
-
-
Ogawa, J.1
Shimizu, S.2
-
226
-
-
0001345246
-
The formation of a novel Pd/ C-ethylenediamine complex catalyst: Hemoselective hydrogenation without deprotection of the O-benzyl and N-cbz groups
-
Sajiki H, Hattori K, Hirora K: The formation of a novel Pd/ C-ethylenediamine complex catalyst: hemoselective hydrogenation without deprotection of the O-benzyl and N-cbz groups. J Org Chem 1998;63(22):7990-2
-
(1998)
J Org Chem
, vol.63
, Issue.22
, pp. 7990-7992
-
-
Sajiki, H.1
Hattori, K.2
Hirora, K.3
-
228
-
-
0242607578
-
-
Patel RN, Nanduri V, Brzozowski D, et al. Enantioselective enzymatic cleavage of N-benzyloxycarbonyl groups. Adv Synthesis Catalysis 2003; 345(6+7):830-4
-
Patel RN, Nanduri V, Brzozowski D, et al. Enantioselective enzymatic cleavage of N-benzyloxycarbonyl groups. Adv Synthesis Catalysis 2003; 345(6+7):830-4
-
-
-
-
229
-
-
0442292081
-
-
Nanduri VB, Goldberg S, Johnston R, et al. Cloning and expression of a novel enantioselective N-carbobenzyloxy-cleaving enzyme. Enzyme Microbial Technol 2004;34(3+4):304-12
-
Nanduri VB, Goldberg S, Johnston R, et al. Cloning and expression of a novel enantioselective N-carbobenzyloxy-cleaving enzyme. Enzyme Microbial Technol 2004;34(3+4):304-12
-
-
-
-
230
-
-
34547169598
-
-
Rudroff F, Rydz J, Ogink FH, et al. Comparing the stereoselective biooxidation of cyclobutanones by recombinant strains expressing bacterial Baeyer-Villiger monooxygenases. Adv Synthesis Catalysis 2007;349(8+9):1436-44
-
Rudroff F, Rydz J, Ogink FH, et al. Comparing the stereoselective biooxidation of cyclobutanones by recombinant strains expressing bacterial Baeyer-Villiger monooxygenases. Adv Synthesis Catalysis 2007;349(8+9):1436-44
-
-
-
-
231
-
-
33646140803
-
Pseudomonad cyclopentadecanone monooxygenase displaying an uncommon spectrum of Baeyer-Villiger oxidations of cyclic ketones
-
Iwaki H, Wang S, Grosse S, et al. Pseudomonad cyclopentadecanone monooxygenase displaying an uncommon spectrum of Baeyer-Villiger oxidations of cyclic ketones. Appl Environ Microbiol 2006;72(4):2707-20
-
(2006)
Appl Environ Microbiol
, vol.72
, Issue.4
, pp. 2707-2720
-
-
Iwaki, H.1
Wang, S.2
Grosse, S.3
-
232
-
-
33646000810
-
Microbial Baeyer-Villiger oxidation of 4,4-disubstituted cyclohexan- and cyclohexenones by recombinant whole-cells expressing monooxygenases of bacterial origin
-
Mihovilovic MD, Snajdrova R, Groetzl B. Microbial Baeyer-Villiger oxidation of 4,4-disubstituted cyclohexan- and cyclohexenones by recombinant whole-cells expressing monooxygenases of bacterial origin. J Mol Catalysis B Enzymatic 2006;39(1-4):135-40
-
(2006)
J Mol Catalysis B Enzymatic
, vol.39
, Issue.1-4
, pp. 135-140
-
-
Mihovilovic, M.D.1
Snajdrova, R.2
Groetzl, B.3
-
233
-
-
33751392312
-
Microbiological transformations 22. Microbiologically mediated Baeyer-Villiger reactions: A unique route to several bicyclic gamma-lactones in high enantiomeric purity
-
Alphand V, Furstoss R. Microbiological transformations 22. Microbiologically mediated Baeyer-Villiger reactions: a unique route to several bicyclic gamma-lactones in high enantiomeric purity. J Org Chem 1989;57:1306-9
-
(1989)
J Org Chem
, vol.57
, pp. 1306-1309
-
-
Alphand, V.1
Furstoss, R.2
-
234
-
-
0242526082
-
Baeyer-Villiger monooxygenases, an emerging family of flavin-dependent biocatalysts
-
Kamberbeek NM, Janssen DB, van Berkel WJH, et al. Baeyer-Villiger monooxygenases, an emerging family of flavin-dependent biocatalysts. Adv Synthesis Catalysis 2003; 345:667-78
-
(2003)
Adv Synthesis Catalysis
, vol.345
, pp. 667-678
-
-
Kamberbeek, N.M.1
Janssen, D.B.2
van Berkel, W.J.H.3
-
235
-
-
0036858978
-
Monooxygenase-mediated Baeyer-Villiger oxidation
-
Mihovilovic MD, Mueller B, Stanetty. Monooxygenase-mediated Baeyer-Villiger oxidation. Eur J Org Chem 2002;22:3711-30
-
(2002)
Eur J Org Chem
, vol.22
, pp. 3711-3730
-
-
Mihovilovic, M.D.1
Mueller, B.2
Stanetty3
-
236
-
-
0031838334
-
Cyclohexanone monooxygenase: A useful reagent for asymmetric Baeyer Villiger reactions
-
Stewart JD. Cyclohexanone monooxygenase: a useful reagent for asymmetric Baeyer Villiger reactions. Curr Org Chem 1998;2:195-216
-
(1998)
Curr Org Chem
, vol.2
, pp. 195-216
-
-
Stewart, J.D.1
-
237
-
-
28844495429
-
Microbial transformations 59: First kilogram scale asymmetric microbial Baeyer-Villiger oxidation with optimized productivity using a resin-based in situ SFPR strategy
-
Hiker I, Wohlgemuth R, Alphand V, et al. Microbial transformations 59: first kilogram scale asymmetric microbial Baeyer-Villiger oxidation with optimized productivity using a resin-based in situ SFPR strategy. Biotechnol Bioeng 2005;92(6):702-10
-
(2005)
Biotechnol Bioeng
, vol.92
, Issue.6
, pp. 702-710
-
-
Hiker, I.1
Wohlgemuth, R.2
Alphand, V.3
-
238
-
-
33745752024
-
Optimizing fermentation conditions of recombinant Escherichia coli expressing cyclopentanone monooxygenase
-
Rudroff F, Alphand V, Furstoss R, et al. Optimizing fermentation conditions of recombinant Escherichia coli expressing cyclopentanone monooxygenase. Org Proc Res Dev 2006;10(3):599-604
-
(2006)
Org Proc Res Dev
, vol.10
, Issue.3
, pp. 599-604
-
-
Rudroff, F.1
Alphand, V.2
Furstoss, R.3
-
239
-
-
34249087442
-
Microbial Baeyer-Villiger oxidation of terpenones by recombinant whole-cell biocatalysts-formation of enantiocomplementary regioisomeric lactones
-
Cernuchova P, Mihovilovic MD. Microbial Baeyer-Villiger oxidation of terpenones by recombinant whole-cell biocatalysts-formation of enantiocomplementary regioisomeric lactones. Org Biomol Chem 2007;5(11):1715-9
-
(2007)
Org Biomol Chem
, vol.5
, Issue.11
, pp. 1715-1719
-
-
Cernuchova, P.1
Mihovilovic, M.D.2
-
240
-
-
3042839971
-
Microbiological transformations 57. Facile and efficient resin-based in situ SFPR preparative-scale synthesis of an enantiopure "unexpected" lactone regioisomer via a Baeyer-Villiger oxidation process
-
Hilker I, Gutierrez MC, Alphand V, et al. Microbiological transformations 57. Facile and efficient resin-based in situ SFPR preparative-scale synthesis of an enantiopure "unexpected" lactone regioisomer via a Baeyer-Villiger oxidation process. Org Lett 2004;6(12):1955-8
-
(2004)
Org Lett
, vol.6
, Issue.12
, pp. 1955-1958
-
-
Hilker, I.1
Gutierrez, M.C.2
Alphand, V.3
-
241
-
-
34547170108
-
-
Pazmino DET, Snajdrova R, Rial DV, et al. Altering the substrate specificity and enantioselectivity of phenylacetone monooxygenase by structure-inspired enzyme redesign. Adv Synthesis Catalysis 2007;349(8+9):1361-8
-
Pazmino DET, Snajdrova R, Rial DV, et al. Altering the substrate specificity and enantioselectivity of phenylacetone monooxygenase by structure-inspired enzyme redesign. Adv Synthesis Catalysis 2007;349(8+9):1361-8
-
-
-
-
242
-
-
84902429400
-
Dynamic kinetic resolution and asymmetric transformations by enzyme-metal combinations
-
Patel RN, editor, CRC Press, FL
-
Kim M-J, Ahn Y, Park J. Dynamic kinetic resolution and asymmetric transformations by enzyme-metal combinations. In: Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 249-72
-
(2007)
Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 249-272
-
-
Kim, M.-J.1
Ahn, Y.2
Park, J.3
-
243
-
-
34047148042
-
Dynamic kinetic resolution catalyzed by enzymes and metals
-
Martin-Mature B, Baeckvall J-E. Dynamic kinetic resolution catalyzed by enzymes and metals. Curr Opin Chem Biol 2007;11(2):226-32
-
(2007)
Curr Opin Chem Biol
, vol.11
, Issue.2
, pp. 226-232
-
-
Martin-Mature, B.1
Baeckvall, J.-E.2
-
244
-
-
39649097521
-
Biocatalytic deracemization: Dynamic resolution, stereoinversion, enantioconvergent processes, and cyclic deracemization
-
Patel RN, editor, CRC Press, FL
-
Simeo Y, Kroutil W, Faber K. Biocatalytic deracemization: dynamic resolution, stereoinversion, enantioconvergent processes, and cyclic deracemization. In: Biocatalysis in the Pharmaceutical and Biotechnology Industries. Patel RN, editor, CRC Press, FL. 2007. p. 27-51
-
(2007)
Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 27-51
-
-
Simeo, Y.1
Kroutil, W.2
Faber, K.3
-
245
-
-
1842473615
-
Enzyme catalyzed deracemization and dynamic kinetic resolution reactions
-
Turner NJ. Enzyme catalyzed deracemization and dynamic kinetic resolution reactions. Curr Opin Chem Biol 2004;8(2):114-9
-
(2004)
Curr Opin Chem Biol
, vol.8
, Issue.2
, pp. 114-119
-
-
Turner, N.J.1
-
246
-
-
0035356381
-
Dynamic kinetic resolution of β-azido alcohols. An efficient route to chiral aziridines and β-amino alcohols
-
Pamies O, Baeckvall J-E. Dynamic kinetic resolution of β-azido alcohols. An efficient route to chiral aziridines and β-amino alcohols. J Org Chem 2001; 66(11):4022-5
-
(2001)
J Org Chem
, vol.66
, Issue.11
, pp. 4022-4025
-
-
Pamies, O.1
Baeckvall, J.-E.2
-
247
-
-
39649117429
-
Synthesis of enantiopure amino acids and amines. Concerted use of a biocatalyst and a chemocatalyst
-
Milan, Italy
-
Archer I, Carr R, Fotheringham I, et al. Synthesis of enantiopure amino acids and amines. Concerted use of a biocatalyst and a chemocatalyst. Chimica e l'Industria (Milan, Italy) 2005;87(6):100-4
-
(2005)
Chimica e l'Industria
, vol.87
, Issue.6
, pp. 100-104
-
-
Archer, I.1
Carr, R.2
Fotheringham, I.3
-
248
-
-
21044439352
-
Directed evolution of oxidase for the preparative deracemization of cyclic secondary amines
-
Carr R, Alexeeva M, Dawson MJ, et al. Directed evolution of oxidase for the preparative deracemization of cyclic secondary amines. Chem Bio Chem 2005;6:637-9
-
(2005)
Chem Bio Chem
, vol.6
, pp. 637-639
-
-
Carr, R.1
Alexeeva, M.2
Dawson, M.J.3
-
249
-
-
1842607456
-
A versatile chemo-enzymatic route to enantiomerically pure β-branched α-amino acids
-
Roff GJ, Lloyd RC, Turner NJ. A versatile chemo-enzymatic route to enantiomerically pure β-branched α-amino acids. J Am Chem Soc 2004;126(13):4098-9
-
(2004)
J Am Chem Soc
, vol.126
, Issue.13
, pp. 4098-4099
-
-
Roff, G.J.1
Lloyd, R.C.2
Turner, N.J.3
-
250
-
-
33846216023
-
Dynamic kinetic resolution of secondary alcohols combining enzyme-catalyzed transesterification and zeolite-catalyzed racemization
-
Zhu Y, Pow K-L, Chuah G-K, et al. Dynamic kinetic resolution of secondary alcohols combining enzyme-catalyzed transesterification and zeolite-catalyzed racemization. Chem A Eur J 2007;13(2):541-7
-
(2007)
Chem A Eur J
, vol.13
, Issue.2
, pp. 541-547
-
-
Zhu, Y.1
Pow, K.-L.2
Chuah, G.-K.3
-
251
-
-
29344468620
-
(S)-selective kinetic resolution and chemoenzymatic dynamic kinetic resolution of secondary alcohols
-
Boren L, Martin-Matute B, Xu Y, et al. (S)-selective kinetic resolution and chemoenzymatic dynamic kinetic resolution of secondary alcohols. Chem A Eur J 2005;12(1):225-32
-
(2005)
Chem A Eur J
, vol.12
, Issue.1
, pp. 225-232
-
-
Boren, L.1
Martin-Matute, B.2
Xu, Y.3
-
252
-
-
8144226976
-
Dynamic kinetic resolution of secondary alcohols by enzyme-metal combinations in ionic liquid
-
Kim M-J, Kim HM, Kim D, et al. Dynamic kinetic resolution of secondary alcohols by enzyme-metal combinations in ionic liquid. Green Chem 2004; 6(9):471-4
-
(2004)
Green Chem
, vol.6
, Issue.9
, pp. 471-474
-
-
Kim, M.-J.1
Kim, H.M.2
Kim, D.3
-
253
-
-
0141757457
-
(S)-Selective dynamic kinetic resolution of secondary alcohols by the combination of subtilisin and an aminocyclopentadienyl ruthenium complex as the catalysts
-
Lee HK, Kim D, Park J. (S)-Selective dynamic kinetic resolution of secondary alcohols by the combination of subtilisin and an aminocyclopentadienyl ruthenium complex as the catalysts. J Am Chem Soc 2003;125:11494-5
-
(2003)
J Am Chem Soc
, vol.125
, pp. 11494-11495
-
-
Lee, H.K.1
Kim, D.2
Park, J.3
-
254
-
-
39649111422
-
-
Verzijl GKM, De Vries JG, Broxterman QB. Process for the preparation of enantiomerically enriched esters and alcohols. WO2001090396 (2001)
-
Verzijl GKM, De Vries JG, Broxterman QB. Process for the preparation of enantiomerically enriched esters and alcohols. WO2001090396 (2001)
-
-
-
-
255
-
-
0035929387
-
Microbial deracemization of 1-aryl and 1-heteroaryl secondary alcohols
-
Allan GR, Carnell AJ. Microbial deracemization of 1-aryl and 1-heteroaryl secondary alcohols. J Org Chem 2001;66(19):6495-7
-
(2001)
J Org Chem
, vol.66
, Issue.19
, pp. 6495-6497
-
-
Allan, G.R.1
Carnell, A.J.2
-
257
-
-
0032555561
-
Deracemization of compounds possessing a sec-alcohol or -amino group through a cyclic oxidation-reduction sequence: A kinetic treatment
-
Kroutil W, Faber K. Deracemization of compounds possessing a sec-alcohol or -amino group through a cyclic oxidation-reduction sequence: a kinetic treatment. Tetrahedron:Asymmetry 1998;9(16):2901-13
-
(1998)
Tetrahedron:Asymmetry
, vol.9
, Issue.16
, pp. 2901-2913
-
-
Kroutil, W.1
Faber, K.2
-
258
-
-
0032611028
-
-
Carnell AJ. Stereoinversions using microbial redox-reactions. Adv Biochem Eng Biotechnol 1999; 63(Biotransformations):57-72
-
Carnell AJ. Stereoinversions using microbial redox-reactions. Adv Biochem Eng Biotechnol 1999; 63(Biotransformations):57-72
-
-
-
-
259
-
-
0037459140
-
Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae
-
Comasseto V, Omori AT, Andrade LH, et al. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae. Tetrahedron:Asymmetry 2003;14:711-5
-
(2003)
Tetrahedron:Asymmetry
, vol.14
, pp. 711-715
-
-
Comasseto, V.1
Omori, A.T.2
Andrade, L.H.3
-
260
-
-
39649117228
-
-
Broxterman QB, Verzijl GKM. Process for the synthesis of (R)-1-(3,5-bis(trifluoromethyl)phenyl) ethan-1-ol and esters thereof by dynamic kinetic resolution. WO2003043575 (2003)
-
Broxterman QB, Verzijl GKM. Process for the synthesis of (R)-1-(3,5-bis(trifluoromethyl)phenyl) ethan-1-ol and esters thereof by dynamic kinetic resolution. WO2003043575 (2003)
-
-
-
-
261
-
-
34547174714
-
Dynamic kinetic resolution of primary alcohols with an unfunctionalized stereogenic center in the β-position
-
Strubing D, Krumlinde P, Piera J, et al. Dynamic kinetic resolution of primary alcohols with an unfunctionalized stereogenic center in the β-position. Adv Synthesis Catalysis 2007;349(10):1577-81
-
(2007)
Adv Synthesis Catalysis
, vol.349
, Issue.10
, pp. 1577-1581
-
-
Strubing, D.1
Krumlinde, P.2
Piera, J.3
-
263
-
-
0037034332
-
Microbial deracemization of α-substituted carboxylic acids
-
Kato D, Mitsuda S, Ohta H. Microbial deracemization of α-substituted carboxylic acids. Org Lett 2002;4:371-3
-
(2002)
Org Lett
, vol.4
, pp. 371-373
-
-
Kato, D.1
Mitsuda, S.2
Ohta, H.3
-
264
-
-
0141677961
-
Microbial deracemization of α-substituted carboxylic acids: Substrate specificity and mechanistic investigation
-
Kato D, Mitsuda S, Ohta H. Microbial deracemization of α-substituted carboxylic acids: substrate specificity and mechanistic investigation. J Org Chem 2003;68:7234-42
-
(2003)
J Org Chem
, vol.68
, pp. 7234-7242
-
-
Kato, D.1
Mitsuda, S.2
Ohta, H.3
-
265
-
-
0037941143
-
An efficient route to chiral α- and β-hydroxyalkanephosphonates
-
Pamies O, Baeckvall JE. An efficient route to chiral α- and β-hydroxyalkanephosphonates. J Org Chem 2003;68(12):4815-18
-
(2003)
J Org Chem
, vol.68
, Issue.12
, pp. 4815-4818
-
-
Pamies, O.1
Baeckvall, J.E.2
-
266
-
-
0030848933
-
Microbiological transformations. 37. An enantioconvergent synthesis of the β-blocker (R)-nifenalol using a combined chemoenzymic approach
-
Paedragosa-Moreau S, Morisseau C, Baratti J, et al. Microbiological transformations. 37. An enantioconvergent synthesis of the β-blocker (R)-nifenalol using a combined chemoenzymic approach. Tetrahedron 1997;53(28):9707-14
-
(1997)
Tetrahedron
, vol.53
, Issue.28
, pp. 9707-9714
-
-
Paedragosa-Moreau, S.1
Morisseau, C.2
Baratti, J.3
-
268
-
-
16144362981
-
Chemoenzymic resolution and deracemization of (±)-1-methyl-1,2-epoxycyclohexane: The synthesis of (1-S,2-S)-I-methylcyclohexane-1,2 diol
-
Archer, IVJ, Leak DJ, Widdowson DA. Chemoenzymic resolution and deracemization of (±)-1-methyl-1,2-epoxycyclohexane: the synthesis of (1-S,2-S)-I-methylcyclohexane-1,2 diol. Tetrahedron Lett 1996;37(48):8819-22
-
(1996)
Tetrahedron Lett
, vol.37
, Issue.48
, pp. 8819-8822
-
-
Archer, I.V.J.1
Leak, D.J.2
Widdowson, D.A.3
-
269
-
-
16444371523
-
A chemoenzymatic, enantioconvergent, asymmetric total synthesis of (R)-fridamycin E
-
Ueberbacher BJ, Osprian I, Mayer SF, et al. A chemoenzymatic, enantioconvergent, asymmetric total synthesis of (R)-fridamycin E. Eur J Org Chem 2005;7:1266-70
-
(2005)
Eur J Org Chem
, vol.7
, pp. 1266-1270
-
-
Ueberbacher, B.J.1
Osprian, I.2
Mayer, S.F.3
-
270
-
-
0347595455
-
Enzymatic transformations. Part 55. Highly productive epoxide hydrolase catalyzed resolution of an azole antifungal key synthon
-
Monfort N, Archelas A, Furstoss R. Enzymatic transformations. Part 55. Highly productive epoxide hydrolase catalyzed resolution of an azole antifungal key synthon. Tetrahedron 2004;60(3):601-5
-
(2004)
Tetrahedron
, vol.60
, Issue.3
, pp. 601-605
-
-
Monfort, N.1
Archelas, A.2
Furstoss, R.3
-
271
-
-
33646518384
-
Properties of epoxide hydrolase from Aspergillus niger for the hydrolytic kinetic resolution of epoxides in pure organic media
-
Karboune S, Archelas A, Baratti J. Properties of epoxide hydrolase from Aspergillus niger for the hydrolytic kinetic resolution of epoxides in pure organic media. Enzyme Microbial Technol 2006;39(2):318-24
-
(2006)
Enzyme Microbial Technol
, vol.39
, Issue.2
, pp. 318-324
-
-
Karboune, S.1
Archelas, A.2
Baratti, J.3
-
272
-
-
0033407110
-
Deracemization of racemic 1,2-diol by biocatalytic stereoinversion
-
Goswami A, Mirfakhrae KD, Patel RN. Deracemization of racemic 1,2-diol by biocatalytic stereoinversion. Tetrahedron: Asymmetry 1999;10(21):4239-44
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, Issue.21
, pp. 4239-4244
-
-
Goswami, A.1
Mirfakhrae, K.D.2
Patel, R.N.3
-
273
-
-
17044392249
-
Kinetic resolution and chemoenzymatic dynamic kinetic resolution of functionalized γ-hydroxy amides
-
Fransson AL, Boren L, Pamies O, et al. Kinetic resolution and chemoenzymatic dynamic kinetic resolution of functionalized γ-hydroxy amides. J Org Chem 2005;70(7):2582-7
-
(2005)
J Org Chem
, vol.70
, Issue.7
, pp. 2582-2587
-
-
Fransson, A.L.1
Boren, L.2
Pamies, O.3
-
274
-
-
10844224531
-
Ruthenium- and enzyme-catalyzed dynamic kinetic asymmetric transformation of 1,4-diols: Synthesis of γ-hydroxy ketones
-
Martin-Mature B, Baeckvall JE. Ruthenium- and enzyme-catalyzed dynamic kinetic asymmetric transformation of 1,4-diols: synthesis of γ-hydroxy ketones. J Org Chem 1994;69(26):9191-5
-
(1994)
J Org Chem
, vol.69
, Issue.26
, pp. 9191-9195
-
-
Martin-Mature, B.1
Baeckvall, J.E.2
-
275
-
-
34347376588
-
A modern view of phenylalanine ammonia lyase
-
MacDonald M, D'Cunha GB. A modern view of phenylalanine ammonia lyase. Biochem Cell Biol 2007;85(3):273-82
-
(2007)
Biochem Cell Biol
, vol.85
, Issue.3
, pp. 273-282
-
-
MacDonald, M.1
D'Cunha, G.B.2
-
277
-
-
0037071912
-
Lipases and (R)-oxynitrilases: Useful tools in organic synthesis
-
Gotor V. Lipases and (R)-oxynitrilases: useful tools in organic synthesis. J Biotechnol 2002;96(1):35-42
-
(2002)
J Biotechnol
, vol.96
, Issue.1
, pp. 35-42
-
-
Gotor, V.1
-
278
-
-
11044237901
-
Hydroxynitrile yases: Biological sources and application as biocatalysts
-
Fechter MH, Griengl H. Hydroxynitrile yases: biological sources and application as biocatalysts. Food Technol Biotechnol 2004;42(4):287-94
-
(2004)
Food Technol Biotechnol
, vol.42
, Issue.4
, pp. 287-294
-
-
Fechter, M.H.1
Griengl, H.2
-
280
-
-
0342796086
-
Syntheses of homochiral cyanohydrins in an industrial environment. Hydroxy nitrile lyases offer new options
-
Poechlauer P. Syntheses of homochiral cyanohydrins in an industrial environment. Hydroxy nitrile lyases offer new options. Chim Oggi 1998;16(5):15-19
-
(1998)
Chim Oggi
, vol.16
, Issue.5
, pp. 15-19
-
-
Poechlauer, P.1
-
282
-
-
39649104424
-
-
Tsuchida T, Nishimoto Y, Kotani T, liizumi K. Jpn Kokai Tokkyo Koho Manufacture of L-3,4-dihydroxyphenylalanine with Erwinia.1993, 7 pp. JP 05123177 A 19930521 Heisei. CAN 119:93708, AN 1993:493708
-
Tsuchida T, Nishimoto Y, Kotani T, liizumi K. Jpn Kokai Tokkyo Koho Manufacture of L-3,4-dihydroxyphenylalanine with Erwinia.1993, 7 pp. JP 05123177 A 19930521 Heisei. CAN 119:93708, AN 1993:493708
-
-
-
-
283
-
-
0013567048
-
Screening for Microbial Biocatalysis
-
Kieslich K, van der Beck CP, deBont JAM, editors, Elsevier:Amsterdam
-
Yamada H. In: Screening for Microbial Biocatalysis. Kieslich K, van der Beck CP, deBont JAM, editors, Studien in Organic Chemistry, Elsevier:Amsterdam 1998;53:13
-
(1998)
Studien in Organic Chemistry
, vol.53
, pp. 13
-
-
Yamada, H.1
-
284
-
-
33745764088
-
Large-scale synthesis of (R)-2-amino-1-(2-furyl)ethanol via a chemoenzymatic approach
-
Purkarthofer T, Pabst T, Van den Broek C, et al. Large-scale synthesis of (R)-2-amino-1-(2-furyl)ethanol via a chemoenzymatic approach. Org Process Res Dev 2006;10(3):618-21
-
(2006)
Org Process Res Dev
, vol.10
, Issue.3
, pp. 618-621
-
-
Purkarthofer, T.1
Pabst, T.2
Van den Broek, C.3
-
285
-
-
34547131285
-
Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry
-
Purkarthofer T, Thomas S, Wolfgang S, et al. Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry. Appl Microbiol Biotechnol 2007;76(2):309-20
-
(2007)
Appl Microbiol Biotechnol
, vol.76
, Issue.2
, pp. 309-320
-
-
Purkarthofer, T.1
Thomas, S.2
Wolfgang, S.3
-
286
-
-
0041590743
-
-
Groger H. Enzymatic routes to enantiomerically pure aromatic α-hydroxy carboxylic acids: a further example for the diversity of biocatalysis. Adv Synthesis Catalysis 2001;343(6+7):547-58
-
Groger H. Enzymatic routes to enantiomerically pure aromatic α-hydroxy carboxylic acids: a further example for the diversity of biocatalysis. Adv Synthesis Catalysis 2001;343(6+7):547-58
-
-
-
-
287
-
-
0142183584
-
Comprehensive step-by-step engineering of an (R)-hydroxynitrile lyase for large-scale asymmetric synthesis
-
Glieder A, Weis R, Skranc W, et al. Comprehensive step-by-step engineering of an (R)-hydroxynitrile lyase for large-scale asymmetric synthesis. Angew Chem Int Ed 2003;42(39):4815-8
-
(2003)
Angew Chem Int Ed
, vol.42
, Issue.39
, pp. 4815-4818
-
-
Glieder, A.1
Weis, R.2
Skranc, W.3
-
288
-
-
39649099667
-
-
Pochlauer P, Schmidt M, Wirth I, et al. Enzymatic process for the preparation of (S)-cyanohydrins. Eur Pat Appl 1999, 14 pp. EP 927766 A1 19990707 CAN 131:72766 AN 1999:440051
-
Pochlauer P, Schmidt M, Wirth I, et al. Enzymatic process for the preparation of (S)-cyanohydrins. Eur Pat Appl 1999, 14 pp. EP 927766 A1 19990707 CAN 131:72766 AN 1999:440051
-
-
-
-
289
-
-
4944231388
-
Hydroxynitrile lyase catalyzed synthesis of heterocyclic (R)- and (S)-cyanohydrins
-
Avi M, Fechter MH, Gruber K, et al. Hydroxynitrile lyase catalyzed synthesis of heterocyclic (R)- and (S)-cyanohydrins. Tetrahedron 2004; 60(46):10411-8
-
(2004)
Tetrahedron
, vol.60
, Issue.46
, pp. 10411-10418
-
-
Avi, M.1
Fechter, M.H.2
Gruber, K.3
-
290
-
-
33846348243
-
Synthesis of optically active cyanohydrins from aromatic ketones: Evidence of an increased substrate range and inverted stereoselectivity for the hydroxynitrile lyase from Linum usitarissimum
-
reduction of
-
Roberge C, Fleitz F, Pllard D, Devine P. Synthesis of optically active cyanohydrins from aromatic ketones: evidence of an increased substrate range and inverted stereoselectivity for the hydroxynitrile lyase from Linum usitarissimum. Tetrahdron Lett 2007;48:1473-7 reduction of
-
(2007)
Tetrahdron Lett
, vol.48
, pp. 1473-1477
-
-
Roberge, C.1
Fleitz, F.2
Pllard, D.3
Devine, P.4
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