Asymmetric anti-Prelog reduction of ketones catalysed by Paracoccus pantotrophus and Comamonas sp. cells via hydrogen transfer
暂无分享,去创建一个
A. Glieder | Alexander Kern | W. Kroutil | I. Lavandera | S. D. Wildeman | Brigitte M Höller | Ursula Ellmer
[1] John M Woodley,et al. New opportunities for biocatalysis: making pharmaceutical processes greener. , 2008, Trends in biotechnology.
[2] A. Glieder,et al. An exceptionally DMSO-tolerant alcohol dehydrogenase for the stereoselective reduction of ketones. , 2008, ChemSusChem.
[3] G. Oberdorfer,et al. Stereocomplementary Asymmetric Reduction of Bulky–Bulky Ketones by Biocatalytic Hydrogen Transfer , 2008 .
[4] Delong Liu,et al. Enantioselective transfer hydrogenation of ketones with planar chiral ruthenocene-based phosphinooxazoline ligands , 2008 .
[5] Hui Lin,et al. Preparation the Key Intermediate of Angiotensin‐Converting Enzyme (ACE) Inhibitors: High Enantioselective Production of Ethyl (R)‐2‐Hydroxy‐4‐Phenylbutyrate with Candida boidinii CIOC21 , 2008 .
[6] H. Pellissier. Recent Developments in Dynamic Kinetic Resolution , 2008 .
[7] R. Stenkamp,et al. X-ray structure and designed evolution of an artificial transfer hydrogenase. , 2008, Angewandte Chemie.
[8] K. Kantardjieff,et al. Inverting the enantioselectivity of a carbonyl reductase via substrate-enzyme docking-guided point mutation. , 2008, Organic letters.
[9] H. Gröger,et al. Practical Two‐Step Synthesis of an Enantiopure Aliphatic Terminal (S)‐Epoxide Based on Reduction of Haloalkanones with “Designer Cells” , 2007 .
[10] Paul N. Devine,et al. Chemo- and enantioselective routes to chiral fluorinated hydroxyketones using ketoreductases. , 2007, Organic letters.
[11] Oliver May,et al. Biocatalytic reductions: from lab curiosity to "first choice". , 2007, Accounts of chemical research.
[12] J. Stewart,et al. Reductions of cyclic β-keto esters by individual Saccharomyces cerevisiae dehydrogenases and a chemo-enzymatic route to (1R,2S)-2-methyl-1-cyclohexanol , 2007 .
[13] Dunming Zhu,et al. Enzymatic ketone reduction: mapping the substrate profile of a short-chain alcohol dehydrogenase (YMR226c) from Saccharomyces cerevisiae , 2007 .
[14] Andreas Liese,et al. Biocatalytic ketone reduction—a powerful tool for the production of chiral alcohols—part I: processes with isolated enzymes , 2007, Applied Microbiology and Biotechnology.
[15] Andreas Liese,et al. Biocatalytic ketone reduction—a powerful tool for the production of chiral alcohols—part II: whole-cell reductions , 2007, Applied Microbiology and Biotechnology.
[16] Wolfgang Kroutil,et al. Enzymatic reduction of ketones in "micro-aqueous" media catalyzed by ADH-A from Rhodococcus ruber. , 2007, Organic letters.
[17] T. Ema,et al. Highly enantioselective and efficient synthesis of methyl (R)-o-chloromandelate with recombinant E. coli: toward practical and green access to clopidogrel. , 2007, Organic & biomolecular chemistry.
[18] M. Beller,et al. New Ruthenium Catalysts for Asymmetric Transfer Hydrogenation of Prochiral Ketones , 2007 .
[19] K. Drauz,et al. Enantioselective reduction of 4-fluoroacetophenone at high substrate concentration using a tailor-made recombinant whole-cell catalyst , 2007 .
[20] Junhua Tao,et al. Recent Advances in Developing Chemoenzymatic Processes for Active Pharmaceutical Ingredients , 2007 .
[21] Paul N. Devine,et al. Enzyme-catalyzed enantioselective diaryl ketone reductions. , 2007, Organic letters.
[22] Dunming Zhu,et al. Enantioselective enzymatic reductions of sterically bulky aryl alkyl ketones catalyzed by a NADPH-dependent carbonyl reductase. , 2006, The Journal of organic chemistry.
[23] Jung Woon Yang,et al. Catalytic asymmetric transfer hydrogenation of alpha-ketoesters with hantzsch esters. , 2006, Organic letters.
[24] H. Adolfsson,et al. Enantioswitchable catalysts for the asymmetric transfer hydrogenation of aryl alkyl ketones. , 2006, Organic letters.
[25] Oliver May,et al. Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. , 2006, Angewandte Chemie.
[26] G. Clarkson,et al. An outstanding catalyst for asymmetric transfer hydrogenation in aqueous solution and formic acid/triethylamine. , 2006, Chemical communications.
[27] Dunming Zhu,et al. Stereoselective ketone reduction by a carbonyl reductase from Sporobolomyces salmonicolor. Substrate specificity, enantioselectivity and enzyme-substrate docking studies. , 2006, Organic & biomolecular chemistry.
[28] N. Iwai,et al. An effective method to use ionic liquids as reaction media for asymmetric reduction by Geotrichum candidum , 2006 .
[29] Christian C. Gruber,et al. Biocatalytic deuterium- and hydrogen-transfer using over-expressed ADH-‘A’: enhanced stereoselectivity and 2H-labeled chiral alcohols , 2006 .
[30] P. Moran,et al. Bioreduction of 2-azido-1-arylethanones mediated by Geotrichum candidum and Rhodotorula glutinis , 2006 .
[31] J. Rozzell,et al. A Two‐Step Chemoenzymatic Synthesis of the Natural Pheromone (+)‐Sitophilure Utilizing Isolated, NADPH‐Dependent Ketoreductases , 2006 .
[32] Dunming Zhu,et al. Enzymatic enantioselective reduction of α-ketoesters by a thermostable 7α-hydroxysteroid dehydrogenase from Bacteroides fragilis , 2006 .
[33] S. Leite,et al. Microbial reduction of ethyl 2-oxo-4-phenylbutyrate. Searching for R-enantioselectivity. New access to the enalapril like ACE inhibitors , 2006 .
[34] W. Kroutil,et al. Regio‐ and Stereoselective Reduction of Diketones and Oxidation of Diols by Biocatalytic Hydrogen Transfer , 2006 .
[35] B. Witholt,et al. Efficient NADPH Recycling in Enantioselective Bioreduction of a Ketone with Permeabilized Cells of a Microorganism Containing a Ketoreductase and a Glucose 6-Phosphate Dehydrogenase , 2006 .
[36] M. Reetz,et al. An efficient catalyst system for the asymmetric transfer hydrogenation of ketones: remarkably broad substrate scope. , 2006, Journal of the American Chemical Society.
[37] J. Sinisterra,et al. Enantioselective production of halohydrin precursor of Propranolol catalysed by immobilized yeasts , 2005 .
[38] Christian C. Gruber,et al. Non‐Racemic Halohydrins via Biocatalytic Hydrogen‐Transfer Reduction of Halo‐Ketones and One‐Pot Cascade Reaction to Enantiopure Epoxides , 2005 .
[39] Y. Makino,et al. Production of (R)-chiral alcohols by a hydrogen-transfer bioreduction with NADH-dependent Leifsonia alcohol dehydrogenase (LSADH) , 2005 .
[40] Ramesh N. Patel,et al. Purification and Cloning of a Ketoreductase used for the Preparation of Chiral Alcohols , 2005 .
[41] A. Chadha,et al. Asymmetric reduction of alkyl 2-oxo-4-arylbutanoates and -but-3-enoates by Candida parapsilosis ATCC 7330: assignment of the absolute configuration of ethyl 2-hydroxy-4-(p-methylphenyl)but-3-enoate by 1H NMR , 2004 .
[42] W. Kroutil,et al. Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols. , 2004, Current opinion in chemical biology.
[43] J. D. Carballeira,et al. Highly stereoselective reduction of haloketones using three new yeasts: application to the synthesis of (S)-adrenergic β-blockers related to propranolol , 2004 .
[44] J. Bäckvall,et al. Chemoenzymatic dynamic kinetic resolution. , 2004, Trends in biotechnology.
[45] Bernhard Hauer,et al. Industrial methods for the production of optically active intermediates. , 2004, Angewandte Chemie.
[46] H. Pellissier. Dynamic Kinetic Resolution , 2003 .
[47] J. Bäckvall,et al. Combination of enzymes and metal catalysts. A powerful approach in asymmetric catalysis. , 2003, Chemical reviews.
[48] W. Kroutil,et al. Enzymatic Racemisation and its Application to Synthetic Biotransformations , 2003 .
[49] W. Kroutil,et al. Biocatalytic asymmetric hydrogen transfer employing Rhodococcus ruber DSM 44541. , 2003, The Journal of organic chemistry.
[50] Yangsoo Ahn,et al. Dynamic kinetic resolutions and asymmetric transformations by enzymes coupled with metal catalysis. , 2002, Current opinion in biotechnology.
[51] Hiroaki Yamamoto,et al. Practical application of recombinant whole-cell biocatalysts for the manufacturing of pharmaceutical intermediates such as chiral alcohols , 2002 .
[52] T. Matsuda,et al. Asymmetric reduction of simple aliphatic ketones with dried cells of Geotrichum candidum , 2002 .
[53] C. Moitzi,et al. Biocatalytic asymmetric hydrogen transfer. , 2002, Angewandte Chemie.
[54] H. Ohta,et al. Microbial asymmetric reduction of α-hydroxyketones in the anti-Prelog selectivity , 2001 .
[55] T. Miura,et al. Asymmetric synthesis of (R)-2-chloro-1-(m-chlorophenyl)ethanol using acetone powder of Geotrichum candidum , 2001, Biotechnology Letters.
[56] Petra Hildebrandt,et al. Efficient resolution of prostereogenic arylaliphatic ketones using a recombinant alcohol dehydrogenase from Pseudomonas fluorescens , 2001 .
[57] Ryoji Noyori,et al. Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones. , 2001, Angewandte Chemie.
[58] A. Medici,et al. Combined microbial oxidation and reduction: a new approach to the highyield synthesis of homochiral unsaturated secondary alcohols from racemates , 1995 .
[59] Karlheinz Drauz,et al. Enzyme Catalysis in Organic Synthesis , 1995 .
[60] A. Klibanov,et al. Asymmetric oxidoreductions catalyzed by alcohol dehydrogenase in organic solvents , 1986 .
[61] V. Prelog. Specification of the stereospecificity of some oxido-reductases by diamond lattice sections , 1964 .
[62] R. Phillips,et al. Asymmetric reduction of ethynyl ketones and ethynylketoesters by secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus , 2000 .
[63] R. Noyori,et al. Quantitative expression of dynamic kinetic resolution of chirally labile enantiomers: stereoselective hydrogenation of 2-substituted 3-oxo carboxylic esters catalyzed by BINAP-ruthenium(II) complexes , 1993 .
[64] Kurt Faber,et al. Biotransformations in Organic Chemistry , 1992 .
[65] S. Servi. Microbial reagents in organic synthesis , 1992 .