The Reaction of α-Substituted Ketones with N-Alkylhydroxylamines
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概要
- 論文の詳細を見る
N-Methyl- and N-benzylhydroxylamine reacted smoothly with ethyl acetoacetate to afford the pyrroline compounds 1 and 2,respectively. On the other hand, the reaction of N-cyclohexylhydroxylamine gave the nitrone compound 3. Other active methylene compounds, i.e., diethyl acetonedicarboxylate, benzoylacetone and nitroacetone, reacted with methylhydroxylamine to give the N-methylpyrrole 6,the nitrone 7 and the isoxazoline 8,respectively.
- 公益社団法人日本薬学会の論文
- 1983-05-25
著者
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佐伯 清太郎
Faculty Of Pharmaceutical Sciences Kyushu University
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浜名 政和
Faculty Of Pharmaceutical Sciences Kyushu University
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本田 晴義
Faculty of Pharmaceutical Sciences, Kyushu University
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本田 晴義
Faculty Of Pharmaceutical Sciences Kyushu University
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