抄録
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.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 31 (5), 1474-1481, 1983
公益社団法人 日本薬学会
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キーワード
詳細情報
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- CRID
- 1390282679142024960
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- NII論文ID
- 130003769302
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- ISSN
- 13475223
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可