スポンサーリンク
Rikagaku Kenkyusho, The Institute of Physical and Chemical Research | 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
- Diterpenoids. XII. Catalytic Hydrogenation of Δ^-and 6-Enol Acetoxyhydrofluorene Derivatives. A Synthesis of Hydrofluorene Derivatives (cis-A/B-Ring Fusion (α C_5-H))
- Diterpenoids. XI. A Synthesis of Hydrofluorene Derivatives (trans-A/B-Ring Fusion (β C_5-H))
- Diterpenoids. X. A Synthesis of c-Homohydrofluorene