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For: Girardin M, Ouellet SG, Gauvreau D, Moore JC, Hughes G, Devine PN, O’shea PD, Campeau L. Convergent Kilogram-Scale Synthesis of Dual Orexin Receptor Antagonist. Org Process Res Dev 2013;17:61-8. [DOI: 10.1021/op3002678] [Cited by in Crossref: 50] [Cited by in F6Publishing: 35] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Richter N, Farnberger JE, Pressnitz D, Lechner H, Zepeck F, Kroutil W. A system for ω-transaminase mediated (R)-amination using l -alanine as an amine donor. Green Chem 2015;17:2952-8. [DOI: 10.1039/c4gc02363c] [Cited by in Crossref: 18] [Article Influence: 2.6] [Reference Citation Analysis]
2 Zeng Z, Zhang J, Jia M, Wu B, Cai X, Zhang X, Feng Y, Ma Y, Gao Q, Fei Z. Development of a Scalable Route with Efficient Stereoisomer Control to YZJ-1139, an Orexin Receptor Antagonist. Org Process Res Dev . [DOI: 10.1021/acs.oprd.1c00457] [Reference Citation Analysis]
3 Meadows RE, Mulholland KR, Schürmann M, Golden M, Kierkels H, Meulenbroeks E, Mink D, May O, Squire C, Straatman H, Wells AS. Efficient Synthesis of ( S )-1-(5-Fluoropyrimidin-2-yl)ethylamine Using an ω-Transaminase Biocatalyst in a Two-Phase System. Org Process Res Dev 2013;17:1117-22. [DOI: 10.1021/op400131h] [Cited by in Crossref: 31] [Cited by in F6Publishing: 22] [Article Influence: 3.4] [Reference Citation Analysis]
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5 Chung JYL, Marcune B, Strotman HR, Petrova RI, Moore JC, Dormer PG. Synthesis of ((3 R ,6 R )-6-Methylpiperidin-3-yl)methanol via Biocatalytic Transamination and Crystallization-Induced Dynamic Resolution. Org Process Res Dev 2015;19:1418-23. [DOI: 10.1021/acs.oprd.5b00259] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.1] [Reference Citation Analysis]
6 Telzerow A, Hobisch M, Müller M, Schürmann M, Schwab H, Steiner K. A co-expression system to shift the equilibrium of transamination reactions toward the synthesis of enantiomerically pure amines. Molecular Catalysis 2019;471:38-43. [DOI: 10.1016/j.mcat.2019.04.006] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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8 Liardo E, Ríos-lombardía N, Morís F, Rebolledo F, González-sabín J. Hybrid Organo- and Biocatalytic Process for the Asymmetric Transformation of Alcohols into Amines in Aqueous Medium. ACS Catal 2017;7:4768-74. [DOI: 10.1021/acscatal.7b01543] [Cited by in Crossref: 29] [Cited by in F6Publishing: 16] [Article Influence: 5.8] [Reference Citation Analysis]
9 Kelly SA, Pohle S, Wharry S, Mix S, Allen CCR, Moody TS, Gilmore BF. Application of ω-Transaminases in the Pharmaceutical Industry. Chem Rev 2018;118:349-67. [PMID: 29251912 DOI: 10.1021/acs.chemrev.7b00437] [Cited by in Crossref: 135] [Cited by in F6Publishing: 92] [Article Influence: 27.0] [Reference Citation Analysis]
10 Ma X, Dewez DF, Du L, Luo X, Markó IE, Lam K. Synthesis of Diketones, Ketoesters, and Tetraketones by Electrochemical Oxidative Decarboxylation of Malonic Acid Derivatives: Application to the Synthesis of cis -Jasmone. J Org Chem 2018;83:12044-55. [DOI: 10.1021/acs.joc.8b01994] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
11 Fuchs CS, Hollauf M, Meissner M, Simon RC, Besset T, Reek JNH, Riethorst W, Zepeck F, Kroutil W. Dynamic Kinetic Resolution of 2-Phenylpropanal Derivatives to Yield β-Chiral Primary Amines via Bioamination. Adv Synth Catal 2014;356:2257-65. [DOI: 10.1002/adsc.201400217] [Cited by in Crossref: 22] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
12 Hollmann F, Opperman DJ, Paul CE. Biokatalytische Reduktionen aus der Sicht eines Chemikers. Angew Chem 2021;133:5706-27. [DOI: 10.1002/ange.202001876] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
13 Simon RC, Richter N, Busto E, Kroutil W. Recent Developments of Cascade Reactions Involving ω-Transaminases. ACS Catal 2014;4:129-43. [DOI: 10.1021/cs400930v] [Cited by in Crossref: 200] [Cited by in F6Publishing: 126] [Article Influence: 22.2] [Reference Citation Analysis]
14 Busto E, Simon RC, Grischek B, Gotor-fernández V, Kroutil W. Cutting Short the Asymmetric Synthesis of the Ramatroban Precursor by Employing ω-Transaminases. Adv Synth Catal 2014;356:1937-42. [DOI: 10.1002/adsc.201300993] [Cited by in Crossref: 27] [Cited by in F6Publishing: 21] [Article Influence: 3.4] [Reference Citation Analysis]
15 Pedragosa-moreau S, Le flohic A, Thienpondt V, Lefoulon F, Petit A, Ríos-lombardía N, Morís F, González-sabín J. Exploiting the Biocatalytic Toolbox for the Asymmetric Synthesis of the Heart-Rate Reducing Agent Ivabradine. Adv Synth Catal 2017;359:485-93. [DOI: 10.1002/adsc.201601222] [Cited by in Crossref: 18] [Cited by in F6Publishing: 11] [Article Influence: 3.6] [Reference Citation Analysis]
16 Wiltschi B, Cernava T, Dennig A, Galindo Casas M, Geier M, Gruber S, Haberbauer M, Heidinger P, Herrero Acero E, Kratzer R, Luley-goedl C, Müller CA, Pitzer J, Ribitsch D, Sauer M, Schmölzer K, Schnitzhofer W, Sensen CW, Soh J, Steiner K, Winkler CK, Winkler M, Wriessnegger T. Enzymes revolutionize the bioproduction of value-added compounds: From enzyme discovery to special applications. Biotechnology Advances 2020;40:107520. [DOI: 10.1016/j.biotechadv.2020.107520] [Cited by in Crossref: 34] [Cited by in F6Publishing: 19] [Article Influence: 17.0] [Reference Citation Analysis]
17 Fuchs CS, Farnberger JE, Steinkellner G, Sattler JH, Pickl M, Simon RC, Zepeck F, Gruber K, Kroutil W. Asymmetric Amination of α-Chiral Aliphatic Aldehydes via Dynamic Kinetic Resolution to Access Stereocomplementary Brivaracetam and Pregabalin Precursors. Adv Synth Catal 2018;360:768-78. [DOI: 10.1002/adsc.201701449] [Cited by in Crossref: 18] [Cited by in F6Publishing: 8] [Article Influence: 3.6] [Reference Citation Analysis]
18 Simić S, Zukić E, Schmermund L, Faber K, Winkler CK, Kroutil W. Shortening Synthetic Routes to Small Molecule Active Pharmaceutical Ingredients Employing Biocatalytic Methods. Chem Rev 2021. [PMID: 34846124 DOI: 10.1021/acs.chemrev.1c00574] [Reference Citation Analysis]
19 van den Biggelaar L, Soumillion P, Debecker DP. Enantioselective Transamination in Continuous Flow Mode with Transaminase Immobilized in a Macrocellular Silica Monolith. Catalysts 2017;7:54. [DOI: 10.3390/catal7020054] [Cited by in Crossref: 27] [Cited by in F6Publishing: 20] [Article Influence: 5.4] [Reference Citation Analysis]
20 Semproli R, Vaccaro G, Ferrandi EE, Vanoni M, Bavaro T, Marrubini G, Annunziata F, Conti P, Speranza G, Monti D, Tamborini L, Ubiali D. Use of Immobilized Amine Transaminase from Vibrio fluvialis under Flow Conditions for the Synthesis of ( S )‐1‐(5‐Fluoropyrimidin‐2‐yl)‐ethanamine. ChemCatChem 2020;12:1359-67. [DOI: 10.1002/cctc.201902080] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
21 Brundiek H, Höhne M. Transaminases - A Biosynthetic Route for Chiral Amines. In: Hilterhaus L, Liese A, Kettling U, Antranikian G, editors. Applied Biocatalysis: From Fundamental Science to Industrial Applications. Weinheim: Wiley-VCH Verlag GmbH & Co. KGaA; 2016. pp. 199-218. [DOI: 10.1002/9783527677122.ch10] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Slabu I, Galman JL, Lloyd RC, Turner NJ. Discovery, Engineering, and Synthetic Application of Transaminase Biocatalysts. ACS Catal 2017;7:8263-84. [DOI: 10.1021/acscatal.7b02686] [Cited by in Crossref: 138] [Cited by in F6Publishing: 68] [Article Influence: 27.6] [Reference Citation Analysis]
23 Schrittwieser JH, Velikogne S, Hall M, Kroutil W. Artificial Biocatalytic Linear Cascades for Preparation of Organic Molecules. Chem Rev 2018;118:270-348. [DOI: 10.1021/acs.chemrev.7b00033] [Cited by in Crossref: 289] [Cited by in F6Publishing: 217] [Article Influence: 57.8] [Reference Citation Analysis]
24 Gand M, Müller H, Wardenga R, Höhne M. Characterization of three novel enzymes with imine reductase activity. Journal of Molecular Catalysis B: Enzymatic 2014;110:126-32. [DOI: 10.1016/j.molcatb.2014.09.017] [Cited by in Crossref: 51] [Cited by in F6Publishing: 36] [Article Influence: 6.4] [Reference Citation Analysis]
25 Sperry JB, Minteer CJ, Tao J, Johnson R, Duzguner R, Hawksworth M, Oke S, Richardson PF, Barnhart R, Bill DR, Giusto RA, Weaver JD. Thermal Stability Assessment of Peptide Coupling Reagents Commonly Used in Pharmaceutical Manufacturing. Org Process Res Dev 2018;22:1262-75. [DOI: 10.1021/acs.oprd.8b00193] [Cited by in Crossref: 43] [Cited by in F6Publishing: 20] [Article Influence: 10.8] [Reference Citation Analysis]
26 Feng J, Geng WC, Jiang H, Wu B. Recent advances in biocatalysis of nitrogen-containing heterocycles. Biotechnol Adv 2022;54:107813. [PMID: 34450199 DOI: 10.1016/j.biotechadv.2021.107813] [Reference Citation Analysis]
27 Busto E, Simon RC, Richter N, Kroutil W. Enzymatic Synthesis of Chiral Amines using ω-Transaminases, Amine Oxidases, and the Berberine Bridge Enzyme. In: Patel RN, editor. Green Biocatalysis. Hoboken: John Wiley & Sons, Inc; 2016. pp. 17-57. [DOI: 10.1002/9781118828083.ch2] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
28 Dunetz JR, Magano J, Weisenburger GA. Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals. Org Process Res Dev 2016;20:140-77. [DOI: 10.1021/op500305s] [Cited by in Crossref: 316] [Cited by in F6Publishing: 181] [Article Influence: 52.7] [Reference Citation Analysis]
29 Kohls H, Steffen-Munsberg F, Höhne M. Recent achievements in developing the biocatalytic toolbox for chiral amine synthesis. Curr Opin Chem Biol 2014;19:180-92. [PMID: 24721252 DOI: 10.1016/j.cbpa.2014.02.021] [Cited by in Crossref: 180] [Cited by in F6Publishing: 151] [Article Influence: 22.5] [Reference Citation Analysis]
30 Velasco-Lozano S, Jackson E, Ripoll M, López-Gallego F, Betancor L. Stabilization of ω-transaminase from Pseudomonas fluorescens by immobilization techniques. Int J Biol Macromol 2020;164:4318-28. [PMID: 32898544 DOI: 10.1016/j.ijbiomac.2020.09.003] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
31 Ríos-Lombardía N, Vidal C, Cocina M, Morís F, García-Álvarez J, González-Sabín J. Chemoenzymatic one-pot synthesis in an aqueous medium: combination of metal-catalysed allylic alcohol isomerisation-asymmetric bioamination. Chem Commun (Camb) 2015;51:10937-40. [PMID: 26062926 DOI: 10.1039/c5cc03298a] [Cited by in Crossref: 38] [Cited by in F6Publishing: 2] [Article Influence: 6.3] [Reference Citation Analysis]
32 Guo F, Berglund P. Transaminase biocatalysis: optimization and application. Green Chem 2017;19:333-60. [DOI: 10.1039/c6gc02328b] [Cited by in Crossref: 214] [Cited by in F6Publishing: 1] [Article Influence: 42.8] [Reference Citation Analysis]
33 Simon RC, Sattler JH, Farnberger JE, Fuchs CS, Richter N, Zepeck F, Kroutil W. Enzymatic asymmetric synthesis of the silodosin amine intermediate. Tetrahedron: Asymmetry 2014;25:284-8. [DOI: 10.1016/j.tetasy.2013.12.012] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 1.6] [Reference Citation Analysis]
34 Moore JC, Rodriguez-Granillo A, Crespo A, Govindarajan S, Welch M, Hiraga K, Lexa K, Marshall N, Truppo MD. "Site and Mutation"-Specific Predictions Enable Minimal Directed Evolution Libraries. ACS Synth Biol 2018;7:1730-41. [PMID: 29782150 DOI: 10.1021/acssynbio.7b00359] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 3.5] [Reference Citation Analysis]
35 Choi J, Han S, Kim H. Industrial applications of enzyme biocatalysis: Current status and future aspects. Biotechnology Advances 2015;33:1443-54. [DOI: 10.1016/j.biotechadv.2015.02.014] [Cited by in Crossref: 430] [Cited by in F6Publishing: 306] [Article Influence: 61.4] [Reference Citation Analysis]
36 Matassa C, Romani A, Ormerod D, Bornscheuer UT, Höhne M, Satyawali Y. Jeffamine® ED‐600: a polyether amine donor for enzymatic transamination in organic solvent/solvent‐free medium with membrane‐assisted product extraction. J Chem Technol Biotechnol 2019;95:604-13. [DOI: 10.1002/jctb.6241] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
37 Sigrist R, da Costa BZ, Marsaioli AJ, de Oliveira LG. Nature-inspired enzymatic cascades to build valuable compounds. Biotechnol Adv 2015;33:394-411. [PMID: 25795056 DOI: 10.1016/j.biotechadv.2015.03.010] [Cited by in Crossref: 31] [Cited by in F6Publishing: 25] [Article Influence: 4.4] [Reference Citation Analysis]
38 Chung JYL, Zhong Y, Maloney KM, Reamer RA, Moore JC, Strotman H, Kalinin A, Feng R, Strotman NA, Xiang B, Yasuda N. Unusual Pyrimidine Participation: Efficient Stereoselective Synthesis of Potent Dual Orexin Receptor Antagonist MK-6096. Org Lett 2014;16:5890-3. [DOI: 10.1021/ol5028249] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 1.1] [Reference Citation Analysis]
39 Zeifman YS, Boyko KM, Nikolaeva AY, Timofeev VI, Rakitina TV, Popov VO, Bezsudnova EY. Functional characterization of PLP fold type IV transaminase with a mixed type of activity from Haliangium ochraceum. Biochim Biophys Acta Proteins Proteom 2019;1867:575-85. [PMID: 30902765 DOI: 10.1016/j.bbapap.2019.03.005] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
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