鈴木真言 | Tanabe Seiyaku Co. Ltd.

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Studies on Streptomyces Antibiotic, Cycloheximide. XVIII. Isomerization Study of Cycloheximides and Thermal Degradation of Naramycin-B. Chemical Support of the Proposed Absolute Configuration of Cycloheximides.
Isomerization Study of Cycloheximides and Thermal Degradation of Naramycin-B. Chemical Proof to the Proposed Absolute Configuration of Cycloheximides
Studies on the Terpenoids and Related Alicyclic Compounds. I. Synthesis of 5α- and 5β-2-Oxosantan-6 : 13-olide from Santonin
Studies on an Antibiotic, Albocycline. III. Partial Structure of Albocycline
Optical Rotatory Dispersion and Circular Dichroism of Securinine and Allosecurinine
Studies on Streptomyces Antibiotic, Cycloheximide. XVI. Synthesis of Cycloheximide Analogous Compounds.
Studies on Streptomyces Antibiotic, Cycloheximide. XV. Hydroxycarbonylation of Optically Active 2,4-Dimethylcyclohexanones with Glutarimide-β-acetaldehyde. : Synthesis of Isocycloheximide and its Isomers.
Absolute Configuration of Cycloheximide
Studies on Streptomyces Antibiotic, Cycloheximide. XI. Preparation and Chemical Structure of the Oxidation Products (ψ-Cycloheximides) from Dihydrocycloheximides
Studies on Streptomyces Antibiotic, Cycloheximide. IX. Absolute Configuration of Optically Active 2,4-Dimethyl-6-(α-hydroxy(ρ-substituted)benzyl) cyclohexanones.
Studies on Streptomyces Antibiotic, Cycloheximide. VIII. Hydroxycarbonylation of Optically Active 2,4-Dimethylcyclohexanone and Chemical Correlation of the Products. (2)
Studies on Streptomyces Antibiotic, Cycloheximide. VIII. Hydroxycarbonylation of Optically Active 2,4-Dimethylcyclohexanone and Chemical Correlation of the Products. (1)
Studies on Streptomyces Antibiotic, Cycloheximide. VII. On the Configuration of Naramycin-B and Isocycloheximide.
Studies on Streptomyces Antibiotic, Cycloheximide. II. Naramycin-B, and Isomer of Cycloheximide.
Studies on Streptomyces Antibiotic, Cycloheximide. I. Isolation of Naramycin-A and its Identification with Cycloheximide
Studies on Cycloheximide and its New Stereoisomeric Antibiotic

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