OHNO Atsuyoshi | Institute for Chemical Research, Kyoto University

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著作論文

Asymmetric Reduction of α-Keto Esters and α-Diketones with a Bakers' Yeast Keto Ester Reductase
Amino Acid Sequence and Characterization of Aldo-keto Reductase from Bakers' Yeast
Purification and Characterization of α-Keto Ester Reductases from Bakers' Yeast
Reactivities of Stable Rotamers. XLI. Reactions of 1-(9-Fluorenyl)-2-(1-methylethenyl)naphthalene Rotamers with Chalcogenyl Halides and Observation of Coloration During the Reaction of Methanesulfenyl Chloride and the ap-Rotamer
Stereochemical Control in Microbial Reduction. 30. Reduction of Alkyl 2-Oxo-4-phenylbutyrate as Precursors of Angiotensin Converting Enzyme (ACE) Inhibitors
Conformational Effect (Induced-Fit) on Catalytic Activity of α-Chymotrypsin
Stereochemical Control in Microbial Reduction. XXIX. Mechanism of Stereochemical Control with an Additive in the Diastereoselective Reduction by Geotrichum candidum
Stereochemical Control in Microbial Reduction. XXV. Additives Controlling Diastereoselectivity in a Microbial Reduction of Ethyl 2-Methyl-3-oxobutanoate
Stereoselective Preparation of (R)-4-Nitro-2-butanol and (R)-5-Nitro-2-pentanol Mediated by a Lipase(Organic Chemistry)
PB124 DIASTEREOSELECTIVE SYNTHESIS OF 2-ALKYL-3-HYDROXYBUTANOATES, USEFUL CHIRAL SYNTHONS, BY MICROBES
Irreversibility of Single Electron Transfer Occurring from Trivalent Phosphorus Compounds to Iron (III) Complexes in the Presence of Ethanol
Reaction of Trivalent Phosphorus Compounds with an Fe (III) Complex in the Presence of Alcohol. Single Electron Transfer Accompanied by a P-O Bond Formation
Stereoelectronic Effects on the One-Electron Donor Reactivity of Trivalent Phosphorus Compounds. Experimental and Theoretical Investigations
Stereochemical Control in Microbial Reduction. XXVIII. Asymmetric Reduction of α,β-Unsaturated Ketones with Bakers' Yeast
NAD(P)^+-NAD(P)H Models. 87. Nonsteric Stereochemistry Controlled by a Carbonyl Dipole
NAD(P)^+-NAD(P)H Models. 86. Nonsteric Stereochemistry in Hydride-Transfer to Sulfinylpyridinium Ion
Reactivity of Cation Radicals Generated from Trivalent-Phosphorus Compounds in the Reaction with Methylviologen: Kinetic Analysis
Stereospecific Electrochemical Oxidation of NAD(P)H Analogs Mediated by Radical Cation of Anilines
Asymmetric Reduction of Butyl Pyruvate Catalyzed by Immobilized Glycerol Dehydrogenase in Organic-Aqueous Biphasic Media
The Catalytic Role of Iodide Ion / Iodine Couple in the Photo-Reduction of 10-Methylacridinium Ion with Diphenylphosphine Oxide
PB23 NAD(P)H MODELS-A HIGHLY SELECTIVE REDUCING REAGENTS IN ORGANIC SYNTHESIS
NAD(P)+-NAD(P)H Models. 49. Proximity effect of a phenyl group on the electron transfer process.

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