Diterpenoids. XXV. Autoxidation of Styrene Type Compounds derived from l-Abietic Acid
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概要
- 論文の詳細を見る
Autoxidation is important phenomenon in the resin acid field. Styrene (III and VIII) and homostyrene (VII) compounds were autoxidized to the corresponding benzonilidene derivatives (IV and IX), which are expected to have interesting reactivity.
- 公益社団法人日本薬学会の論文
- 1973-03-25
著者
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田原 昭
Rikagaku Kenkyusho (The Institute of Physical and Chemical Research)
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大沢 富彦
Rikagaku Kenkyusho (the Institute Of Physical And Chemical Research)
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河原 元雄
Rikagaku Kenkyusho (The Institute of Physical and Chemical Research)
関連論文
- Diterpenoids. XXXV. A-Ring Substitution of Hydrofluorene Compound derived from l-Abietic Acid
- Diterpenoids. XXXIV. Stereochemistry on the Rearranged Compound (Benzilic Acid Rearrangement) of Methyl 6,7-Dioxo-5α, 10α-podocarpa-8,11,13-trien-15-oate
- Stereochemistry on the Rearranged Compound (Benzilic Acid Rearrangement) of Methyl 6,7-Dioxo-5α, 10α-podocarpa-8,11,13-trien-15-oate
- 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. 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.
- Conformational Studies. I. Nuclear Magnetic Resonance Analysis on Conformation of 10β-and 10α-Oxy-enantio-deoxypodocarpic Acid Type Isomer.
- 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
- Diterpenoids. XLV. Ozonolysis of Phenolic Dehydroabietic Acid Derivatives
- Diterpenoids. XLI. Rearrangement of Deisopropyl Phenacylidene Type Diterpene by Means of Aluminum Chloride
- Diterpenoids. XXXVII. Rearrangement of Methyl 13-Isopropyl-7-oxo-podocarpa-5,8,11,13-tetraen-15-oate by Means of Aluminum Chloride
- Diterpenoids. XXX. Reaction of Methyl Dehydroabietate Derivatives with Aluminum Chloride under Effect of Electron-donating Group
- Diterpenoids. XXIX. Nitration of Methyl Dehydroabietate Derivatives
- Diterpenoids. XXVIII. Nitration of Methyl 7-Oxo-dehydroabietate Derivatives
- Novel Nitration Reaction of Methyl 7-Oxodehydroabietate
- 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
- Diterpenoids. XLVI. Syntheses of Taxodione, Royleanone and Their Analogues
- Diterpenoids. XXXVI. Synthesis of d-Kaurene and d-Phyllocladene from l-Abietic Acid
- Transformation of l-Abietic Acid to Benzohydroazulene Derivative
- 32 Dehydroabietic AcidよりSteroid骨格の合成研究
- Diterpenoids. XLII. Stereoselective Synthesis of d-Phyllocladene from l-Abietic Acid
- Diterpenoids. XXXVIII. Conversion of l-Abietic Acid into Steroidal Skeletons : Formation of the D-Ring (1)
- Diterpenoids. XXVII. Synthesis of 11-Methoxy-diterpenoids. (2). Synthesis of 11-Methoxy-dehydroabietic Acid Derivatives
- Diterpenoids. XXVI. Synthesis of 11-Methoxy-diterpenoids. (1). Synthesis of Antipodal 11-Methoxy-deoxypodocarpic Acid Derivatives
- Diterpenoides. XXI. Hydration of Stereoisomers of Dimethyl 1,2,3,4,5,10,11,14-Octahydro-4β, 10α-dimethyl-fluorene-4α, 6-dicarboxylate
- Diterpenoids. XX. Nitration of Dimethyl 1,2,3,10-Tetrahydro-4β, 10α-dimethyl-4H-fluorene-4α, 6-dicarboxylate and Its Hydrogenated Stereoisomers
- Diterpenoids. XVII. Epimerization at Lactonization of 6β-Hydroxy-enantio-podocarpan (and 8-monoen-) 16-oic Acid (cis-and trans-B/C-ring Juncture) Syntheses of the Corresponding 6α-Hydroxy Series
- Lactonization of 6β-Hydroxy-tetrahydro-and-hexahydro-enantio-deoxypodocarpic Acid. Synthesis of 6α-Hydroxy-tetrahydro-and-hexahydro-enantio-deoxypodocarpic Acid
- Diterpenoids. XXV. Autoxidation of Styrene Type Compounds derived from l-Abietic Acid
- Diterpenoids. XXIV. Transformation of Podocarpic Acid Type Diterpene to B-Homo-C-nor-5β, 10α-podocarpan Skeleton
- Conversion of Dehydroabietic Acid into a Steroid Skeleton : Formation of the D-Ring. II
- Conversion of Dehydroabietic Acid into a Steroid Skeleton : Formation of the A-ring. III.
- Conversion of Dehydroabietic Acid into a Steroid Skeleton : Formation of the A-Ring. II
- Conversion of Dehydroabietic Acid into a Steroid Skeleton : Formation of the A-Ring. I
- Study on Synthesis of Antipodal Steroid
- Synthesis of Four Possible Isomers of 4β, 10-Dimethyl-1,2,3,4,5,10-hexahydrofluorene-4,6-dicarboxylic Acid Derivatives
- Transformation of Abietic Acid to the Hydrofluorene Derivatives