Oka Shinzaburo | Institute For Chemical Research Kyoto University

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PB124 DIASTEREOSELECTIVE SYNTHESIS OF 2-ALKYL-3-HYDROXYBUTANOATES, USEFUL CHIRAL SYNTHONS, BY MICROBES
Reduction by a model of NAD(P)H. XIV. Mechanistic consideration on the role of metal ion.
Effect of catalyst on the oxygenation of styrene with BH4- and molecular oxygen.
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.
Reduction by a model of NAD(P)H. 34. Substituent effect on asymmetric reduction of trifluoroacetophenones.
Reduction by a model of NAD(P)H. 32. Stereoselective reduction of camphoroquinone by a chiral NAD(P)H model.
Reduction by a model of NAD(P)H. 35. Spectroscopic detection of charge-transfer intermediate.
NAD(P)+-NAD(P)H model. 63. Regioselective reduction of dienoic ketones and aldehydes with an NAD(P)H model on silica gel.
Stereochemical control in microbial reduction. 8. Stereochemical control in microbial reduction of .BETA.-keto esters.
The transition-metal catalyzed dehalogenation of aromatic halides by NaOH-alcohols. A facile method of destroying aromatic polyhalides.
Stereochemical control in microbial reduction. 9. Diastereoselective reduction of 2-alkyl-3-oxobutanoate with bakers' yeast.
A kinetic study of the reaction of 1-propyl-1,4-dihydronicotinamide with hexacyanoferrate(III).
Reduction by a model of NAD(P)H. 36. First and direct evidence for the multi-step mechanism.

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