Stereochemistry in the Hydrogenation of Steroidal(22R)- and (22S)-Δ^<24>-26,22-Lactones
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概要
- 論文の詳細を見る
Catalytic hydrogenation of the (22R)-unsaturated loctone 8 and its (22S)-epimer 9 afforded stereoselectively the (22R, 24R)-saturated lactone 10 and the (22S, 24S)-isomer 11,respectively. The C-24 stereochemistry of the hydrogenated products was determined by their conversion into 24-ethylcholesterols.
- 公益社団法人日本薬学会の論文
- 1986-05-25
著者
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池川 信夫
新潟薬科大学
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池川 信夫
Department Of Chemistry Tokyo Institute Of Technology
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藤本 善徳
Department of Chemistry, Tokyo Institute of Technology
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藤本 善徳
Department Of Chemistry Tokyo Institute Of Technology
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蒲生 啓司
Department Of Chemistry Tokyo Institute Of Technology
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岩舘 裕
Department of Chemistry, Tokyo Institute of Technology
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岩舘 裕
Department Of Chemistry Tokyo Institute Of Technology
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