Ring Transformation of 2-Furylcarbamates to 5-Hydroxy-3-pyrrolin-2-ones
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概要
- 論文の詳細を見る
N-Ethoxycarbonyl- and N-benzyloxycarbonyl-5-hydroxy-5-methoxyalkylpyrrolinones (6a-c) and (7a-c) together with minor products 8-10 were obtained from the photooxidation or autoxidation of corresponding 2-furylcarbamates (4a-c) and (5a-c). The catalytic hydrogenation of 6a-c afforded saturated γ-ketoamides (11a-c), while that of 7a-c led to the formation of 5-hydroxypyrrolidones (12a-c).
- 社団法人日本薬学会の論文
- 1986-05-25
著者
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古川 宏
名城大・薬
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鈴木 理香
Faculty Of Pharmacy Meiji University
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古川 宏
Faculty of Pharmacy, Meijo University
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薬師神 健一
Faculty Of Pharmacy Meiji University
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古川 宏
Faculty Of Pharmacy Meijo University
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川口 直子
Faculty of Pharmacy, Meiji University
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坪井 良憲
Faculty of Pharmacy, Meiji University
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坪井 良憲
Faculty Of Pharmacy Meiji University
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薬師神 健一
名城大学薬学部
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川口 直子
Faculty Of Pharmacy Meiji University
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