Diterpenoids. XLV. Ozonolysis of Phenolic Dehydroabietic Acid Derivatives
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概要
- 論文の詳細を見る
Ozonolysis of phenolic dehydroabietic acid derivatives with an isopropyl group at 13-position was investigated and the direction of cleavage of the aromatic ring by means of ozonolysis was found to be affected by the substitution pattern of hydroxyl group in the aromatic ring. Ozonolysis of the 12-hydroxy ester (12) afforded the pentanorlabdane type compounds, (13), (14), and (15), while ozonolysis of the 14-hydroxy ester (17) and (18) gave the drimane type products, (19) and (20).
- 公益社団法人日本薬学会の論文
- 1977-05-25
著者
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秋田 弘幸
Riken Institute (The Institute of Physical and Chemical Research)
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田原 昭
Rikagaku Kenkyusho (The Institute of Physical and Chemical Research)
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秋田 弘幸
Rikagaku Kenkyusho (The Institute of Physical and Chemical Research)
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田原 昭
Rikagaku Kenkyusho (the Institute Of Physical Chemical Research)
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森 和彦
Rikagaku Kenkyusho (the Institute Of Physical And Chemical Research):(present Address)science Univer
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