Pure and Applied Chemistry

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• Kędziora Kinga, Bisogno Fabricio R., Lavandera Iván, Gotor-Fernández Vicente, Montejo-Bernardo Jose, García-Granda Santiago, Kroutil Wolfgang, Gotor Vicente: Expanding the Scope of Alcohol Dehydrogenases towards Bulkier Substrates: Stereo- and Enantiopreference for α,α-Dihalogenated Ketones. ChemCatChem 2014, n/a. <http://dx.doi.org/10.1002/cctc.201300834>
• Deasy Rebecca E., Maguire Anita R.: Baker's-Yeast-Mediated Reduction of Sulfur-Containing Compounds. Eur. J. Org. Chem. 2014, n/a. <http://dx.doi.org/10.1002/ejoc.201301729>
• Itoh Nobuya: Use of the anti-Prelog stereospecific alcohol dehydrogenase from Leifsonia and Pseudomonas for producing chiral alcohols. Appl Microbiol Biotechnol 2014, 98, 3889. <http://dx.doi.org/10.1007/s00253-014-5619-5>
• Man Henry, Kędziora Kinga, Kulig Justyna, Frank Annika, Lavandera Iván, Gotor-Fernández Vicente, Rother Dörte, Hart Sam, Turkenburg Johan P., Grogan Gideon: Structures of Alcohol Dehydrogenases from Ralstonia and Sphingobium spp. Reveal the Molecular Basis for Their Recognition of ‘Bulky–Bulky’ Ketones. Top Catal 2014, 57, 356. <http://dx.doi.org/10.1007/s11244-013-0191-2>
• Liu Xu, Chen Rong, Yang Zhongwei, Wang Jiale, Lin Jinping, Wei Dongzhi: Characterization of a Putative Stereoselective Oxidoreductase from Gluconobacter oxydans and Its Application in Producing Ethyl (R)-4-Chloro-3-Hydroxybutanoate Ester. Mol Biotechnol 2014, 56, 285. <http://dx.doi.org/10.1007/s12033-013-9707-z>
• Itoh Nobuya, Isotani Kentaro, Makino Yoshihide, Kato Masaki, Kitayama Kouta, Ishimota Tuyoshi: PCR-based amplification and heterologous expression of Pseudomonas alcohol dehydrogenase genes from the soil metagenome for biocatalysis. Enzyme and Microbial Technology 2014, 55, 140. <http://dx.doi.org/10.1016/j.enzmictec.2013.10.012>
• Patel Jay M., Phillips Robert S.: Effects of Hydrostatic Pressure on Stereospecificity of Secondary Alcohol Dehydrogenase from Thermoanaerobacter Ethanolicus Support the Role of Solvation in Enantiospecificity. ACS Catal. 2014, 4, 692. <http://dx.doi.org/10.1021/cs4010997>
• Rodríguez Cristina, Borzęcka Wioleta, Sattler Johann H., Kroutil Wolfgang, Lavandera Iván, Gotor Vicente: Steric vs. electronic effects in the Lactobacillus brevis ADH-catalyzed bioreduction of ketones. Org. Biomol. Chem. 2014, 12, 673. <http://dx.doi.org/10.1039/c3ob42057d>
• Häckh Matthias, Müller Michael, Lüdeke Steffen: Substrate-Dependent Stereospecificity of Tyl-KR1: An Isolated Polyketide Synthase Ketoreductase Domain from Streptomyces fradiae. Chem. Eur. J. 2013, 19, 8922. <http://dx.doi.org/10.1002/chem.201300554>
• Yamamoto Hiroaki, Kudoh Masatake: Novel chiral tool, (R)-2-octanol dehydrogenase, from Pichia finlandica: purification, gene cloning, and application for optically active α-haloalcohols. Appl Microbiol Biotechnol 2013, 97, 8087. <http://dx.doi.org/10.1007/s00253-012-4643-6>
• Zhang Rui, Ren Jie, Wang Yu, Wu Qiaqing, Wang Min, Zhu Dunming: Isolation and characterization of a novel Rhodococcus strain with switchable carbonyl reductase and para-acetylphenol hydroxylase activities. J Ind Microbiol Biotechnol 2013, 40, 11. <http://dx.doi.org/10.1007/s10295-012-1199-5>
• Liang Ping, Qin Bin, Mu Mao, Zhang Xin, Jia Xian, You Song: Prelog and anti-Prelog stereoselectivity of two ketoreductases from Candida glabrata. Biotechnol Lett 2013, 35, 1469. <http://dx.doi.org/10.1007/s10529-013-1228-0>
• Sethi Madhuresh K., Bhandya Somashekar R., Kumar Anish, Maddur Nagaraj, Shukla Rohit, Jayalakshmi Mittapalli V.S.N.: Chemo-enzymatic synthesis of optically pure rivastigmine intermediate using alcohol dehydrogenase from baker's yeast. Journal of Molecular Catalysis B: Enzymatic 2013, 91, 87. <http://dx.doi.org/10.1016/j.molcatb.2013.02.010>
• de Souza de Oliveira Camila, de Andrade Kleber Tellini, Omori Alvaro Takeo: One-pot chemoenzymatic synthesis of chiral disubstituted 1,2,3-triazoles in aqueous media. Journal of Molecular Catalysis B: Enzymatic 2013, 91, 93. <http://dx.doi.org/10.1016/j.molcatb.2013.03.004>
• Sethi Madhuresh K., Bhandya Somashekar R., Maddur Nagaraj, Shukla Rohit, Kumar Anish, Jayalakshmi Mittapalli V.S.N.: Asymmetric synthesis of an enantiomerically pure rivastigmine intermediate using ketoreductase. Tetrahedron: Asymmetry 2013, 24, 374. <http://dx.doi.org/10.1016/j.tetasy.2013.01.023>
• Vitale Paola, D’Introno Cinzia, Perna Filippo Maria, Perrone Maria Grazia, Scilimati Antonio: Kluyveromyces marxianus CBS 6556 growing cells as a new biocatalyst in the asymmetric reduction of substituted acetophenones. Tetrahedron: Asymmetry 2013, 24, 389. <http://dx.doi.org/10.1016/j.tetasy.2013.02.001>
• Rowan Andrew S., Moody Thomas S., Howard Roger M., Underwood Toby J., Miskelly Iain R., He Yanan, Wang Bo: Preparative access to medicinal chemistry related chiral alcohols using carbonyl reductase technology. Tetrahedron: Asymmetry 2013, 24, 1369. <http://dx.doi.org/10.1016/j.tetasy.2013.09.015>
• Agudo Rubén, Roiban Gheorghe-Doru, Reetz Manfred T.: Induced Axial Chirality in Biocatalytic Asymmetric Ketone Reduction. J. Am. Chem. Soc. 2013, 135, 1665. <http://dx.doi.org/10.1021/ja3092517>
• Reetz Manfred T.: Biocatalysis in Organic Chemistry and Biotechnology: Past, Present, and Future. J. Am. Chem. Soc. 2013, 135, 12480. <http://dx.doi.org/10.1021/ja405051f>
• Brenna Elisabetta, Gatti Francesco G., Malpezzi Luciana, Monti Daniela, Parmeggiani Fabio, Sacchetti Alessandro: Synthesis of Robalzotan, Ebalzotan, and Rotigotine Precursors via the Stereoselective Multienzymatic Cascade Reduction of α,β-Unsaturated Aldehydes. J. Org. Chem. 2013, 78, 4811. <http://dx.doi.org/10.1021/jo4003097>
• Schrittwieser Joerg H., Coccia Francesca, Kara Selin, Grischek Barbara, Kroutil Wolfgang, d'Alessandro Nicola, Hollmann Frank: One-pot combination of enzyme and Pd nanoparticle catalysis for the synthesis of enantiomerically pure 1,2-amino alcohols. Green Chem. 2013, 15, 3318. <http://dx.doi.org/10.1039/c3gc41666f>
• Ramos Aline de Souza, Ribeiro Joyce Benzaquem, Lopes Raquel de Oliveira, de Souza Rodrigo Octavio Mendonça Alves: Whole Cells in Enantioselective Reduction of tert-Butyl Acetoacetate. Synthetic Communications 2013, 43, 1611. <http://dx.doi.org/10.1080/00397911.2012.655685>
• Jakoblinnert A., Wachtmeister J., Schukur L., Shivange A. V., Bocola M., Ansorge-Schumacher M. B., Schwaneberg U.: Reengineered carbonyl reductase for reducing methyl-substituted cyclohexanones. Protein Engineering Design and Selection 2013, 26, 291. <http://dx.doi.org/10.1093/protein/gzt001>
• Cuetos Aníbal, Rioz-Martínez Ana, Bisogno Fabricio R., Grischek Barbara, Lavandera Iván, de Gonzalo Gonzalo, Kroutil Wolfgang, Gotor Vicente: Access to Enantiopure α-Alkyl-β-hydroxy Esters through Dynamic Kinetic Resolutions Employing Purified/Overexpressed Alcohol Dehydrogenases. Adv. Synth. Catal. 2012, 354, 1743. <http://dx.doi.org/10.1002/adsc.201200139>
• Itoh Nobuya, Isotani Kentaro, Nakamura Masatoshi, Inoue Kousuke, Isogai Yasuhiro, Makino Yoshihide: Efficient synthesis of optically pure alcohols by asymmetric hydrogen-transfer biocatalysis: application of engineered enzymes in a 2-propanol–water medium. Appl Micobiol Biotechnol 2012, 93, 1075. <http://dx.doi.org/10.1007/s00253-011-3447-4>
• Liu Xiang, Wang Yi, Gao Hai Yan, Xu Jian He: Asymmetric reduction of α-hydroxy aromatic ketones to chiral aryl vicinal diols using carrot enzymes system. Chinese Chemical Letters 2012, 23, 635. <http://dx.doi.org/10.1016/j.cclet.2012.04.001>
• Trif Maria, Kalló Noémi Hajnalka, Naghi Mara Ana, Bencze László Csaba: Stereoselective bioreduction of 1-(5-phenylfuran-2-yl)-ethanones mediated by baker's yeast. Biocatalysis Biotransformation 2012, 30, 177. <http://dx.doi.org/10.3109/10242422.2011.638374>
• Bencze László Csaba, Paizs Csaba, Toşa Monica Ioana, Irimie Florin Dan, Rétey János: Chemoenzymatic One-Pot Synthesis of both (R)- and (S)-Aryl-1,2-ethanediols. ChemCatChem 2011, 3, 343. <http://dx.doi.org/10.1002/cctc.201000295>
• Hamzic Melissa, Pietruszka Jörg, Sandkuhl Diana: HPLC-CD selectivity assay for alcohol dehydrogenases. Chirality 2011, 23, E110. <http://dx.doi.org/10.1002/chir.21025>
• Wang Li-Juan, Li Chun-Xiu, Ni Yan, Zhang Jie, Liu Xiang, Xu Jian-He: Highly efficient synthesis of chiral alcohols with a novel NADH-dependent reductase from Streptomyces coelicolor. Bioresource Technology 2011, 102, 7023. <http://dx.doi.org/10.1016/j.biortech.2011.04.046>
• Pace Vittorio, Cabrera Álvaro Cortés, Ferrario Valerio, Sinisterra José V., Ebert Cynthia, Gardossi Lucia, Braiuca Paolo, Alcántara Andrés R.: Structural bases for understanding the stereoselectivity in ketone reductions with ADH from Thermus thermophilus: A quantitative model. Journal of Molecular Catalysis B: Enzymatic 2011, 70, 23. <http://dx.doi.org/10.1016/j.molcatb.2011.01.017>
• Salvi Neeta A., Chattopadhyay Subrata: Rhizopus arrhizus-mediated asymmetric reduction of arylalkanones: unusual anti-Prelong products with benzyl alkyl ketones. Tet Asymm 2011, 22, 1512. <http://dx.doi.org/10.1016/j.tetasy.2011.08.015>
• García-Urdiales Eduardo, Alfonso Ignacio, Gotor Vicente: Update 1 of: Enantioselective Enzymatic Desymmetrizations in Organic Synthesis. Chemistry Review 2011, 111, PR110. <http://dx.doi.org/10.1021/cr100330u>
• Berti Federico, Bincoletto Simone, Donati Ivan, Fontanive Giampaolo, Fregonese Massimo, Benedetti Fabio: Albumin-directed stereoselective reduction of 1,3-diketones and β-hydroxyketones to anti diols. Org Biomol Chem 2011, 9, 1987. <http://dx.doi.org/10.1039/c0ob00648c>
• Nie Yao, Xiao Rong, Xu Yan, Montelione Gaetano T.: Novel anti-Prelog stereospecific carbonyl reductases from Candida parapsilosis for asymmetric reduction of prochiral ketones. Org Biomol Chem 2011, 9, 4070. <http://dx.doi.org/10.1039/c0ob00938e>
• Musa Musa M., Phillips Robert S.: Recent advances in alcohol dehydrogenase-catalyzed asymmetric production of hydrophobic alcohols. Catal Sci Technol 2011, 1, 1311. <http://dx.doi.org/10.1039/c1cy00160d>
• KAWANO Shigeru, YANO Miho, HASEGAWA Junzo, YASOHARA Yoshihiko: Cloning and Overexpression of an NADH-Dependent Alcohol Dehydrogenase Gene from Candida maris Involved in (R)-Selective Reduction of 5-Acetylfuro[2,3-c]pyridine. Biosciences Biotechnology and Biochemistry 2011, 75, 2155. <http://dx.doi.org/10.1271/bbb.110453>
• Freyne E. J., Esmans E. L., Vanbroeckhoven J. H., Lepoivre J. A., Alderweireldt F. C.: Synthesis of a novel β-NAD+ analogue: 3-Ac-5-Me-PyrAD+. Bull Soc Chim Belges 2010, 87, 801. <http://dx.doi.org/10.1002/bscb.19780871010>
• van Osselaer T. A., Lemière G. L., Lepoivre J. A., Alderweireldt F. C.: Enzymatic in vitro reduction of ketones VI. (1) reduction rates and stereochemistry of the HLAD-catalyzed reduction of 3-alkyl- and 4-alkylcyclohexanones. Bull Soc Chim Belges 2010, 89, 133. <http://dx.doi.org/10.1002/bscb.19800890209>
• van Osselaer T. A., Lemière G. L., Lepoivre J. A., Alderweireldt F. C.: Enzymatic “In Vitro” Reduction of Ketones VII.(1) Reduction rates and stereochemistry of the HLAD catalyzed reduction of 2-alkyl cyclohexanones, dimethyl cyclohexanones, cycloalkanones and bicycloalkanones. Bull Soc Chim Belges 2010, 89, 389. <http://dx.doi.org/10.1002/bscb.19800890510>
• Zilbeyaz Kani, Kurbanoglu Esabi B.: Highly enantiomeric reduction of acetophenone and its derivatives by locally isolated Rhodotorula glutinis. Chirality 2010, 22, 849. <http://dx.doi.org/10.1002/chir.20846>
• Zhi-Liang Wei, Zu-Yi Li, Guo-Qiang Ijn: Microbial reduction of sulfur-containing ketones by Geotrichum sp. Chin J Chem 2010, 18, 249. <http://dx.doi.org/10.1002/cjoc.20000180221>
• Wang Ke, Li Jin-Feng, Yuan Cheng-Ye, Li Zu-Yi: Regio- and Stereo-selective Bioreduction of Diketo-n-butylphosphonate by Baker's Yeast. Chin J Chem 2010, 20, 1379. <http://dx.doi.org/10.1002/cjoc.20020201138>
• Pei-Ran Chen, Jian-Xin Gu, Zbi-Liang Wei, Shi-Qing Han, Zn-Yi Li, Guo-Qiang Lin: Asymmetric Syntheses Aided by Biocatalysts. Chin J Chem 2010, 21, 983. <http://dx.doi.org/10.1002/cjoc.20030210802>
• Zheng Guo-Jun, Gao Xiao-Lei, Chen Jin-Chun, Li Yu-Lin: Baker's Yeast Mediated Reduction of Optically Active Diketone. Chin J Chem 2010, 22, 191. <http://dx.doi.org/10.1002/cjoc.20040220217>
• van Ramesdonk H. J., Verhoeven J. W., Pandit U. K., de Boer Th. J.: Asymmetric reductions by a chiral pyridine-dinucleotide model. Recl Trav Chim Pays-Bas 2010, 97, 195. <http://dx.doi.org/10.1002/recl.19780970706>
• Rioz-Martínez Ana, Bisogno Fabricio R., Rodríguez Cristina, de Gonzalo Gonzalo, Lavandera Iván, Torres Pazmiño Daniel E., Fraaije Marco W., Gotor Vicente: Biocatalysed concurrent production of enantioenriched compounds through parallel interconnected kinetic asymmetric transformations. Org Biomol Chem 2010, 8, 1431. <http://dx.doi.org/10.1039/b925377g>
• Protsko Carla, Vieille Claire, Laivenieks Maris, Prasad Lata, Sanders David A. R., Delbaere Louis T. J.: Crystallization and preliminary X-ray diffraction analysis of the Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase I86A mutant. Acta Crystallogr F Struct Biol Cryst Commun 2010, 66, 831. <http://dx.doi.org/10.1107/S1744309110018981>
• Zhu Dunming, Hua Ling: How carbonyl reductases control stereoselectivity: Approaching the goal of rational design. Pure and App Chemis 2010, 1. <http://dx.doi.org/10.1351/PAC-CON-09-01-03>
• Musa Musa M., Lott Nathan, Laivenieks Maris, Watanabe Leandra, Vieille Claire, Phillips Robert S.: A Single Point Mutation Reverses the Enantiopreference of Thermoanaerobacter ethanolicus Secondary Alcohol Dehydrogenase. ChemCatChem 2009, 1, 89. <http://dx.doi.org/10.1002/cctc.200900033>
• Asako Hiroyuki, Shimizu Masatoshi, Itoh Nobuya: Biocatalytic production of (S)-4-bromo-3-hydroxybutyrate and structurally related chemicals and their applications. Appl Microbiol Biotechnol 2009, 84, 397. <http://dx.doi.org/10.1007/s00253-009-2105-6>
• Kira Ikuo, Onishi Norimasa: Purification and characterization of a (S)-1-phenyl-1, 3-propanediol-producing enzyme from Williopsis saturnus var. mrakii AJ-5620. J Biosci Bioengin 2009, 107, 116. <http://dx.doi.org/10.1016/j.jbiosc.2008.10.010>
• Lin Hui, Chen Yong-Zheng, Xu Xiao-Ying, Xia Shi-Wen, Wang Li-Xin: Preparation of key intermediates of adrenergic receptor agonists: Highly enantioselective production of (R)-α-halohydrins with Saccharomyces cerevisiae CGMCC 2.396. Mol Catal B Enzym 2009, 57, 1. <http://dx.doi.org/10.1016/j.molcatb.2008.06.003>
• Orden Alejandro A., Magallanes-Noguera Cynthia, Agostini Elizabeth, Kurina-Sanz Marcela: Anti-Prelog reduction of ketones by hairy root cultures. Mol Catal B Enzym 2009, 61, 216. <http://dx.doi.org/10.1016/j.molcatb.2009.07.007>
• de Freitas Araujo Daniel M., Vieira Gizelle A.B., de Mattos Marcos Carlos, Lemos Telma L.G., de Oliveira Maria da Conceição F., Melo Vânia M.M., de Gonzalo Gonzalo, Gotor-Fernández Vicente, Gotor Vicente: Chemoenzymatic preparation of a biologically active naphthoquinone from Tabebuia impetiginosa using lipases or alcohol dehydrogenases. Mol Catal B Enzym 2009, 61, 279. <http://dx.doi.org/10.1016/j.molcatb.2009.08.006>
• Kayser Margaret M.: ‘Designer reagents’ recombinant microorganisms: new and powerful tools for organic synthesis. Tetrahedron 2009, 65, 947. <http://dx.doi.org/10.1016/j.tet.2008.10.039>
• Schrittwieser Joerg H., Lavandera Iván, Seisser Birgit, Mautner Barbara, Lutje Spelberg Jeffrey H., Kroutil Wolfgang: Shifting the equilibrium of a biocatalytic cascade synthesis to enantiopure epoxides using anion exchangers. Tet Asymm 2009, 20, 483. <http://dx.doi.org/10.1016/j.tetasy.2009.02.035>
• Pinedo-Rivilla Cristina, Cafêu Mariana Carrara, Casatejada Josefina Aleu, Araujo Ângela Regina, Collado Isidro G.: Asymmetric microbial reduction of ketones: absolute configuration of trans-4-ethyl-1-(1S-hydroxyethyl)cyclohexanol. Tet Asymm 2009, 20, 2666. <http://dx.doi.org/10.1016/j.tetasy.2009.11.001>
• Ng Jeck Fei, Jaenicke Stephan: Immobilized Whole Cells as Effective Catalysts for Chiral Alcohol Production. Aust J Chem 2009, 62, 1034. <http://dx.doi.org/10.1071/CH09112>
• KIRA Ikuo, ONISHI Norimasa: Purification and Characterization of a (R)-1-Phenyl-1,3-propanediol-producing Enzyme from Trichosporon fermentans AJ-5152 and Enzymatic (R)-1-Phenyl-1,3-propanediol Production. Biosci Biotechnol Biochem 2009, 73, 1640. <http://dx.doi.org/10.1271/bbb.90159>
• Sorgedrager Menno J., van Rantwijk Fred, Huisman Gjalt W., Sheldon Roger A.: Asymmetric Carbonyl Reductions with Microbial Ketoreductases. Adv Synth Catal 2008, 350, 2322. <http://dx.doi.org/10.1002/adsc.200800200>
• Höllrigl Volker, Hollmann Frank, Kleeb Andreas C., Buehler Katja, Schmid Andreas: TADH, the thermostable alcohol dehydrogenase from Thermus sp. ATN1: a versatile new biocatalyst for organic synthesis. Appl Microbiol Biotechnol 2008, 81, 263. <http://dx.doi.org/10.1007/s00253-008-1606-z>
• Wallner Sabine R., Lavandera Iván, Mayer Sandra F., Öhrlein Reinhold, Hafner Andreas, Edegger Klaus, Faber Kurt, Kroutil Wolfgang: Stereoselective anti-Prelog reduction of ketones by whole cells of Comamonas testosteroni in a ‘substrate-coupled’ approach. Mol Catal B Enzym 2008, 55, 126. <http://dx.doi.org/10.1016/j.molcatb.2008.02.009>
• Hoyos Pilar, Sansottera Giacomo, Fernández María, Molinari Francesco, Sinisterra José Vicente, Alcántara Andrés R.: Enantioselective monoreduction of different 1,2-diaryl-1,2-diketones catalysed by lyophilised whole cells from Pichia glucozyma. Tetrahedron 2008, 64, 7929. <http://dx.doi.org/10.1016/j.tet.2008.06.019>
• Salvi Neeta A., Chattopadhyay Subrata: Asymmetric reduction of halo-substituted arylalkanones with Rhizopus arrhizus. Tet Asymm 2008, 19, 1992. <http://dx.doi.org/10.1016/j.tetasy.2008.07.035>
• Lavandera Iván, Höller Brigitte, Kern Alexander, Ellmer Ursula, Glieder Anton, de Wildeman Stefaan, Kroutil Wolfgang: Asymmetric anti-Prelog reduction of ketones catalysed by Paracoccus pantotrophus and Comamonas sp. cells via hydrogen transfer. Tet Asymm 2008, 19, 1954. <http://dx.doi.org/10.1016/j.tetasy.2008.08.005>
• Yadav J.S., Reddy B.V. Subba, Sreelakshmi Ch., Narayana Kumar G.G.K.S., Rao A. Bhaskar: Enantioselective reduction of 2-substituted tetrahydropyran-4-ones using Daucus carota plant cells. Tetrahetron Lett 2008, 49, 2768. <http://dx.doi.org/10.1016/j.tetlet.2008.02.131>
• Musa Musa M., Ziegelmann-Fjeld Karla I., Vieille Claire, Phillips Robert S.: Activity and selectivity of W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus in organic solvents and ionic liquids: mono- and biphasic media. Org Biomol Chem 2008, 6, 887. <http://dx.doi.org/10.1039/b717120j>
• Musa Musa M., Ziegelmann-Fjeld Karla I., Vieille Claire, Zeikus J. Gregory, Phillips Robert S.: Xerogel-Encapsulated W110A Secondary Alcohol Dehydrogenase fromThermoanaerobacter ethanolicus Performs Asymmetric Reduction of Hydrophobic Ketones in Organic Solvents. Angew Chem 2007, 119, 3151. <http://dx.doi.org/10.1002/ange.200604615>
• Musa Musa M., Ziegelmann-Fjeld Karla I., Vieille Claire, Zeikus J. Gregory, Phillips Robert S.: Xerogel-Encapsulated W110A Secondary Alcohol Dehydrogenase fromThermoanaerobacter ethanolicus Performs Asymmetric Reduction of Hydrophobic Ketones in Organic Solvents. Angew Chem Int Ed 2007, 46, 3091. <http://dx.doi.org/10.1002/anie.200604615>
• Pękala; Elżbieta, Godawska-Matysik Anna, Żelaszczyk Dorota: Enantioselective reduction of pentoxifylline to lisofylline using whole-cell Lactobacillus kefiri biotransformation. Biotechnol J 2007, 2, 492. <http://dx.doi.org/10.1002/biot.200600236>
• Itoh Nobuya, Nakamura Masatoshi, Inoue Kousuke, Makino Yoshihide: Continuous production of chiral 1,3-butanediol using immobilized biocatalysts in a packed bed reactor: promising biocatalysis method with an asymmetric hydrogen-transfer bioreduction. Appl Microbiol Biotechnol 2007, 75, 1249. <http://dx.doi.org/10.1007/s00253-007-0957-1>
• Rodríguez Paula, Barton María, Aldabalde Virginia, Onetto Silvia, Panizza Paola, Menéndez Pilar, Gonzalez David, Rodríguez Sonia: Are endophytic microorganisms involved in the stereoselective reduction of ketones by Daucus carota root?. Mol Catal B Enzym 2007, 49, 8. <http://dx.doi.org/10.1016/j.molcatb.2007.06.011>
• Ghanem Ashraf: Trends in lipase-catalyzed asymmetric access to enantiomerically pure/enriched compounds. Tetrahedron 2007, 63, 1721. <http://dx.doi.org/10.1016/j.tet.2006.09.110>
• Yadav Jhillu S., Reddy Garudammagari S.K.K., Sabitha Gowravaram, Krishna Avvaru D., Prasad Attaluri R., Hafeez-U-R-Rahaman, Vishwaswar Rao Katta, Bhaskar Rao Adari: Daucus carota and baker’s yeast mediated bio-reduction of prochiral ketones. Tet Asymm 2007, 18, 717. <http://dx.doi.org/10.1016/j.tetasy.2007.03.009>
• Bisel Philippe, Walter Lydia, Nieger Martin, Hummel Werner, Müller Michael: Stereochemical clarification of the enzyme-catalysed reduction of 2-acetylchromen-4-one. Tet Asymm 2007, 18, 1142. <http://dx.doi.org/10.1016/j.tetasy.2007.05.003>
• Kurbanoglu Eshabi B., Zilbeyaz Kani, Kurbanoglu Namudar I., Kilic Hamdullah: Enantioselective reduction of substituted acetophenones by Aspergillus niger. Tet Asymm 2007, 18, 1159. <http://dx.doi.org/10.1016/j.tetasy.2007.05.017>
• Kurbanoglu Esabi B., Zilbeyaz Kani, Kurbanoglu Namudar I., Kilic Hamdullah: Asymmetric reduction of acetophenone analogues by Alternaria alternata using ram horn peptone. Tet Asymm 2007, 18, 2332. <http://dx.doi.org/10.1016/j.tetasy.2007.09.009>
• Collado Isidro González, Sánchez Antonio José Macías, Hanson James R.: Fungal terpene metabolites: biosynthetic relationships and the control of the phytopathogenic fungus Botrytis cinerea. Nat Prod Rep 2007, 24, 674. <http://dx.doi.org/10.1039/b603085h>
• Kratzer Regina, Nidetzky Bernd: Identification of Candida tenuis xylose reductase as highly selective biocatalyst for the synthesis of aromatic ?-hydroxy esters and improvement of its efficiency by protein engineering. Chem Commun 2007, 1047. <http://dx.doi.org/10.1039/b616475g>
• Nie Y., Xu Y., Yang M., Mu X.-Q.: A novel NADH-dependent carbonyl reductase with unusual stereoselectivity for (R)-specific reduction from an (S)-1-phenyl-1,2-ethanediol-producing micro-organism: purification and characterization. Lett Appl Microbiol 2007, 44, 555. <http://dx.doi.org/10.1111/j.1472-765X.2006.02100.x>
• Chu Linda, Johnston Robert M., Patel Ramesh N., Goldberg Steven L., Nanduri Venkata B.: 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 Microbiology Technology 2006, 39, 1441. <http://dx.doi.org/10.1016/j.enzmictec.2006.03.033>
• Fardelone Lucídio C., Rodrigues J. Augusto R., Moran Paulo J.S.: Bioreduction of 2-azido-1-arylethanones mediated by Geotrichum candidum and Rhodotorula glutinis. Mol Catal B Enzym 2006, 39, 9. <http://dx.doi.org/10.1016/j.molcatb.2006.01.015>
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