Diterpenoids. XIV. Conformational Studies. II. Preferred Conformation of A/B-cis Ring-C Aromatic Tricyclic Diterpenes
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概要
- 論文の詳細を見る
Syntheses of 20-nor tricyclic diterpene derivatives and determination of their structures are described. In the A/B-cis ring system, it is revealed by the analysis of proton magnetic resonance, infrared spectrum and reaction that the steroid type conformation of 10-methyl series is preferred to nonsteroid type conformation, conversely, nonsteroid type conformation is preferred in 20-nor derivatives.
- 公益社団法人日本薬学会の論文
- 1970-10-25
著者
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田原 昭
Rikagaku Kenkyusho (The Institute of Physical and Chemical Research)
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平尾 健一
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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平尾 健一
Rikagaku Kenkyusho The Institute Of Physical And Chemical Research
関連論文
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