尾崎茂子 | Faculty Of Pharmaceutical Sciences Osaka University

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著作論文

EPOXIDATION CATALYZED BY Mn(III)TPPC1 USING DIOXYGEN ACTIVATED BY A NOVEL SYSTEM CONTAINING N-HYDROXYPHTHALIMIDE AND STYRENE(Communications to the Editor)
Anodic Oxidation of Amines. IX. Anodic Oxidation Process of α-Amino Acids in Aqueous Buffer of pH 10
A SIMPLE ELECTROCHEMICAL OXIDATION OF ALDEHYDE ACETALS TO ESTERS IN EUTRAL SOLUTION
Anodic Oxidation of Amides and Lactams Using N-Hydroxyphthalimide as a Mediator
Electrochemical Oxidation of Olefins Using N-Hydroxyphthalimide as a Mediator
Oxidation of Hydroxylamine Derivatives. VI. Anodic Oxidation of N-Alkyl-β-hydroxyhydroxylamines in Aqueous Buffer Solution
Indirect Electroreductive Sequential Radical Reaction Catalyzed by a Ni(II) Complex. One-Step Preparation of Functionalized (Methylene)cyclopentanes
Indirect Electroreductive Cyclization of N-Allyl and N-Propargylamides Using a Nickel(II) Complex as an Electron-Transfer Catalyst : Selective Formation of Halogenated and Non-halogenated Pyrrolidinones
Electroreductive Synthesis of Bicyclic Ketones Mediated by Cobalt or Nickel Complexes
Anodic Oxidation of Amines. VIII. Oxidation of Ethane-1,2-diamines
ANODIC OXIDATION OF COMPOUNDS HAVING BENZYLIC OR ALLYLIC CARBON AND α-CARBON TO HETERO ATOM USING N-HYDROXYPHTHALIMIDE AS A MEDIATOR
Acylation of Amines and Alcohols by Anodic Oxidation of N-Phenyl-hydroxamic Acids
CORRECT MOLECULAR STRUCTURE OF THE PRODUCT OBTAINED FROM THE REACTION OF ACETYLSALICYLOYLCHLORIDE WITH N-PHENYLHYDROXYLAMINE. ELECTROCHEMICAL AND X-RAY CRYSTALLOGRAPHIC STUDIES
Oxidative Bond Fission of β-Alkanolamines by Chlorine Dioxide and the Effect of an Oxymethylene Group at the β-Carbon on the Reaction
Oxidation Potential of Hydroxamic Acids and 4-Fluorophenol in the Presence of Added Base. Effect of Hydrogen-bonding
Anodic Oxidation of Amines. VII. Oxidation of β-Alkanolamines in Aqueous Buffer of pH 10
Oxidation Potential Shift as a Measure of Hydrogen-Bonding and/or the Basicity
Anodic Oxidation of Amines. VI. Revised Reaction Scheme for the Oxidation of Ephedrine
Oxidation of N-Alkylhydroxylamines. IV. Anodic Oxidation of N-Alkylhydroxylamines
Oxidation of Hydroxylamine Derivatives. IV. Anodic Oxidation of Cycloserine and Its Acetyl Derivatives in Aqueous Buffer Solution
Oxidation of Hydroxylamine Derivatives. III. Anodic Oxidation of N-Hydoxy and N-Alkoxycarbamates
Oxidation of N-Alkylhydroxylamines. III. Reaction of N-Alkylhydroxylamines with 1,1-Diphenyl-2-picrylhydrazyl
Studies on the Nuclear Magnetic Resonance Spectra in Aromatic Systems. VII. Preliminary Discussions on the Coupling Constants in Substituted Aromatics
Studies on the Nuclear Magnetic Resonance Spectra in Aliphatic Systems. I. Preliminary Discussions on the Chemical Shifts of Alkyl Derivatives
Anodic Oxidation of Amines. V. Cyclic Voltammetry and Controlled Potential Electrolysis of Ephedrine and the Related Compounds in Aqueous Buffer Solution
Oxidation of Hydroxylamine Derivatives. II. Anodic Oxidation of Phenylhydroxylamines
Oxidation of Hydroxylamine Derivatives. I. Anodic Oxidation of Hydroxamic Acids
Oxidation of N-Alkylhydroxylamines. II. Reaction of N-Alkylhydroxylamines with tert-Butylhydroperoxide
Oxidation of N-Alkylhydroxylamines. I. Nitroxides formed on Oxidation of N-Alkylhydroxylamines with Lead Tetraacetate

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