Heterocycles by cycloaddition. III. Dihydroisoindolequinone, the correct structure of the proposed azatetracyclononanedione.
スポンサーリンク
概要
- 論文の詳細を見る
Pyrolysis of a cyclopentadienequinone–oxazolone adduct (<B>3</B>) gives a 5,6-dihydro-4,7-isoindolequinone (<B>7</B>) and not an azatetracyclic cage compound (<B>4</B>). The dihydroquinone (<B>7</B>) was dehydrogenated to the corresponding isoindolequinone (<B>9</B>), which was synthesized <I>via</I> alternative routes.
- 公益社団法人 日本化学会の論文
著者
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Kato Hiroshi
Department Of Applied Biological Chemistry Graduate School Of Agricultural And Life Sciences The Uni
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Matsukubo Hiroshi
Department of Chemistry, Faculty of Science, Shinshu University
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Kato Hiroshi
Department of Chemistry, Faculty of Science, Shinshu University
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