Nakamura Kaoru | Institute For Chemical Research Kyoto University

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著作論文

Further Characterization of Earthworm Serine Proteases : Cleavage Specificity Against Peptide Substrates and on Autolysis
Multi-enzymatic Glucosylation Using Eucalyptus UDP-Glucosyltransferase Coupled UDPglucose-Fermentation by Bakers'Yeast
Asymmetric Reduction of α-Keto Esters and α-Diketones with a Bakers' Yeast Keto Ester Reductase
Lipase-catalyzed Synthesis of Arbutin Cinnamate in an Organic Solvent and Application of Transesterification to Stabilize Plant Pigments
Preparation of Optically Active α-Hydroxy Esters : Stereoselective Reduction of α-Keto Esters Using Thermophilic Actinomycetes
Amino Acid Sequence and Characterization of Aldo-keto Reductase from Bakers' Yeast
Stereoselective Reduction of α- and β-Keto Esters with Aerobic Thermophiles, Bacillus Strains
Protein Sequences of Two Keto Ester Reductases: Possible Identity as Hypothetical Proteins
Enzymatic Production of (S)-1-Acetoxy-2-Alkanol with Bakers' Yeast Cell-Free Extract in a Membrane Reactor
Purification and Characterization of α-Keto Ester Reductases from Bakers' Yeast
Differences in Protein Structure and Similarities in Catalytic Function of Two L-Stereoselective Carbonyl Reductases from Bakers' Yeast
Detoxifying Effect of Desalinated Deep Seawater on Organotin-poisoned Euglena gracilis(Food & Nutrition Science)
Detoxification Effect of Iron-encaging Zeolite-processed Water in Tributyltin-intoxicated Euglena gracilis Z
Effect of Several Solutions Including Mineral-encaging Zeolites on the Restoration of Cell Motility of Tributyltin-intoxicated Euglena gracilis Z
First Principles Calculations of Vacancy Formation Energies in *13 Pyramidal Twin Grain Boundary of α-Al_2O_3
Stereochemical Control in Microbial Reduction. 30. Reduction of Alkyl 2-Oxo-4-phenylbutyrate as Precursors of Angiotensin Converting Enzyme (ACE) Inhibitors
The NADPH : Quinone Oxidoreductase P1-ζ-crystallin in Arabidopsis Catalyzes the α, β-Hydrogenation of 2-Alkenals : Detoxication of the Lipid Peroxide-Derived Reactive Aldehdes
Stereoselective Preparation of (R)-4-Nitro-2-butanol and (R)-5-Nitro-2-pentanol Mediated by a Lipase(Organic Chemistry)
Rate Enhancement of Lipase-catalyzed Reaction in Supercritical Carbon Dioxide
PB124 DIASTEREOSELECTIVE SYNTHESIS OF 2-ALKYL-3-HYDROXYBUTANOATES, USEFUL CHIRAL SYNTHONS, BY MICROBES
Asymmetric Reduction of Butyl Pyruvate Catalyzed by Immobilized Glycerol Dehydrogenase in Organic-Aqueous Biphasic Media
Lipase-Catalyzed Transesterification of Aryl-Substituted Alkanols in an Organic Solvent
Stereoselective Synthesis of (±)-Isonitramine and (±)-Sibirine
A new, highly efficient, and simple procedure for the construction of medium-sized nitrogen heterocyclic ring system.
Charge-transfer intermediate in the reaction of thioketone with nucleophiles.
NAD(P)+-NAD(P)H models. 65. Photochemical reductive desulfonylation of .BETA.-keto sulfones with Hantzsch ester.
NAD(P)+-NAD(P)H models. 59 1,2- Versus 1,4-reduction of .BETA.,.GAMMA.-unsaturated .ALPHA.-keto ester.
Stereochemical control in microbial reduction. Part 7. Enantioselective reduction of 2-methyl-3-oxopropionate by bakers' yeast.
NAD(P)+-NAD(P)H model. 54. Free radical mechanism for the reductive debromination of vic-dibromides to alkenes.
Stereochemical control in microbial reduction. 12. (S)-4-nitro-2-butanol as a source to synthesize natural products.
Reduction by a model of NAD(P)H. 34. Substituent effect on asymmetric reduction of trifluoroacetophenones.
Enhanced enantioselectivity of the lipase-catalyzed hydrolysis by the addition of a catalytic amount of an amino alcohol.
Stereochemistry of NAD(P)-coenzyme in the reaction catalyzed by glycerol dehydrogenase.
Stereochemical control in microbial reduction. XV. Preparation of (2R, 3S)-2-allyl-3-hydroxybutanoate.
NAD(P)+-NAD(P)H model. 63. Regioselective reduction of dienoic ketones and aldehydes with an NAD(P)H model on silica gel.
Reduction by a model of NAD(P)H. 36. First and direct evidence for the multi-step mechanism.
Reaction of electrochemically generated radical anion of thioketone with alkylating agents.
Stereochemical Control in Microbial Reduction. 18. Mechanism of Stereochemical Control in the Diastereoselective Reduction with Bakers' Yeast.

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