平尾健一 | Rikagaku Kenkyusho The Institute Of Physical And Chemical Research

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著作論文

Diterpenoids. XVI. Reduction of 6β-Hydroxy-enantio-podocarpa-8,11,13-trien-16-oic Acid Derivative
Synthesis of 6β Hydroxy-tetrahydro-and-hexahydroenantio-deoxypodocarpic Acid
Diterpenoids. XV. Conformational Studies. III. Temperature Dependent Proton Magnetic Resonance Spectra of Ring C Aromatic Tricyclic Diterpene
Diterpenoids. XIV. Conformational Studies. II. Preferred Conformation of A/B-cis Ring-C Aromatic Tricyclic Diterpenes
Diterpenoids. IX. Chemical Conversion to Diterpene Alkaloid from Abietic Acid.
Diterpenoids. VIII. Synthesis of Skeleton of Diterpene Alkaloid.
22 Tricyclic Diterpene(Aromatic C-Ring)系のConformation
Conformational Studies. I. Nuclear Magnetic Resonance Analysis on Conformation of 10β-and 10α-Oxy-enantio-deoxypodocarpic Acid Type Isomer.
21.Diterpene Alkaloidの完全合成 : Abietic Acidよりの関連
Diterpenoids. VII. Study on Catalytic Hydrogenations of Methyl 9-Oxo-10-hydroxypodocarpa-5,7,10,13-tetraen-16-oate Enantiomer Type Compounds
Study on the Chemical Shifts for the Methyl Groups of Deoxypodocarpic Acid (Enantiomer) Type Compounds and Syntheses of their 10β-15 or 10α-17 Epoxy Derivatives
Selective Oxidation of the C_1- or C_-Methyl Group in Antipodal Deoxypodocarpic Acid Type Compounds
Resin酸における2,3の研究

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