The Alkylation of 3,5-Dimethylisoxazole
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概要
- 論文の詳細を見る
3,5-Dimethylisoxazole (<B>1</B>) was alkylated with sodium amide in liquid ammonia to give 3-methyl-5-alkylisoxazoles. By di- and tri-alkylation reactions using excess sodium amide, isoxazoles having secondary and tertiary alkyl groups at 5-position could be obtained. The hydrogenolysis and hydrolysis of these isoxazoles were also studied.
- 公益社団法人 日本化学会の論文
著者
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Yamamoto Makoto
Department Of Bacteriology National Institute Of Health
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Sugiyama Noboru
Department of Chemistry Faculty of Science Tokyo University of Education
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Kashima Choji
Department of Chemistry, The University of Tsukuba
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Tobe Shinji
Department of Chemistry, Tokyo Kyoiku University
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