牧角徳夫 | Shionogi Research Laboratories 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.
Studies on Fused Indoles. II. Structural Modifications and Analgesic Activity of 4-Aminomethyltetrahydrothiopyrano [2,3-b] indoles
2-トリアゾリルシクロアルカノール誘導体の立体および光学異性体の抗菌および植物生長阻害活性
Synthesis of Potential Anticancer Agents. II. Halogenation of 7-Substituted 5-Methyl-s-triazolo [2,3-a] pyrimidines
Indole Grignard Reaction. III. : Synthesis, Crystal Structure, and Aalgesic Activity of (R)-and (S)-3-Amino-2,3,4,9-tetrahydrothiopyrano[2,3-b]indoles
Studies on Fused Indoles. I. Novel Synthesis of 4-Aminomethyltetrahydrothiopyrano [2,3-b] indoles through a Thio-Claisen Rearrangement
A New Indole Synthesis via Rearrangements of N-Propargylaniline N-Oxides. A One-pot Synthesis of Indole-3-acetonitriles
The Claisen Rearrangement in Aromatic Heterocyclic Compounds. II. The Thermal Rearrangement of Allyl 4-Quinolyl Ethers
The Claisen Rearrangement in Aromatic Heterocyclic Compounds. I. The ortho-Claisen Rearrangement of Allyl, Methallyl, and Crotyl Ethers of 2-Methyl-4-quinolinol
Studies on Azaindolizine Compounds. XVIII. Proton Magnetic Resonance Spectra of s-Triazolo-[1,5-α] pyrimidine and its Derivatives.
Studies on Azaindolizine Compounds. XVI. The Allyl Rearrangement of 7-Allyloxy-5,6-dimethyls-triazolo [1,5-a] pyrimidime.
Studies on Azaindolizine Compounds. XV. The Allyl Rearrangement of 5-Methyl-7-allyloxys-triazolo [1,5-a] pyrimidine.
Studies on Azaindolizine Compounds. XIV. Transetherification in s-Triazolo [1,5-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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