牧角徳夫 | Research Laboratory, Shionogi & Co., Ltd.

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著作論文

On the Action of Substituted Azaindolizines on Microorganisms. III. Action of Aminated Azaindolizines on Lactic Acid Bacteria.
Action of Substituted Azaindolizines on Microorganisms. I. Action on Lactic Acid Bacteria.
Synthesis of Potential Anticancer Agents. II. Halogenation of 7-Substituted 5-Methyl-s-triazolo [2,3-a] pyrimidines
Studies on the Azaindolizine Compounds. XIII. Alkylation of 5-Methyl-s-triazolo [1,5-a] pyrimidin-7-ol.
Studies on the Azaindolizine Compounds. XII. Alkyl Rearrangement of 5-Methyl-7-alkoxy-s-triazolo [1,5-a] pyrimidines.
Studies on the Azaindolizine Compounds. XI. Synthesis of 6,7-Disubstituted Pyrazolo [1,5-a] pyrimidines.
Studies on the Azaindolizine Compounds. X. Synthesis of 5,7-Disubstituted Pyrazolo [1,5-a] pyrimidines.
Synthesis of Potential Anticancer Agents. IX. Condensation of some 2-, 5-, and 7-Methyl-s-triazolo [2,3-α] pyrimidines with Benzaldehyde.
Synthesis of Potential Anticancer Agents. VIII. 6-Phenylazo-s-triazolo [2,3-α] pyrimidines.
Synthesis of Potential Anticancer Agents. VII. 6-Nitro- and 6-Amino-s-triazolo [2,3-α] pyrimidines.
Synthesis of Potential Anticancer Agents. VI. Reactivity of 6-Bromo-s-triazolo [2,3-a] pyrimidines.
Synthesis of Potential Anticancer Agents. V. 6-Halo-s-triazolo [2,3-a] pyrimidines.
Synthesis of Potential Anticancer Agents. IV. 5,7-Disubstituted s-Triazolo [2,3-a] pyrimidines.
Synthesis of Potential Anticancer Agents. III. 7-Substituted s-Triazolo [2,3-a]-pyrimidines and their Halogenated Compounds
Synthesis of Potential Anticancer Agents. I. 5-Substituted 7-Methyl-s-triazolo [4,3-α]-and-tetrazolo [1,5-α]-pyrimidines.
Studies on Isoxazole Derivatives. XI. Synthesis of 4-Ethoxycarbonyl-and 4-Cyano-5-aminoisoxazoles and Their Ring Cleavage.
Isoxazole誘導体の研究(第8報)5-Aminoisoxazole類の接触還元

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