exo-Selective peripheral cycloaddition reactions of pyrido(2,1-a)isoindole.
スポンサーリンク
概要
- 論文の詳細を見る
Pyrido[2,1-<I>a</I>]isoindole cycloadds to olefinic dipolarophiles in a highly <I>exo</I>-selective fashion giving the kinetically controlled cycloadducts which gradually isomerize into the Michael adducts. With acetylenic dipolarophiles, the hydrogen-migrated cycloadducts are the only products. The mechanism of cycloadditions is discussed.
- 公益社団法人 日本化学会の論文
著者
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Mori Seiji
Department Of Chemistry The University Of Tokyo
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Kajigaeshi Shoji
Department Of Applied Chemistry And Chemical Engineering Faculty Of Engineering Yamaguchi University
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Fujisaki Shizuo
Department Industrial Chemistry
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Mori Seiji
Department of Industrial Chemistry, Faculty of Engineering, Yamaguchi University
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Kanemasa Shuji
Research Institute of Industrial Science, and Department of Molecular Science and Technology, Interdisciplinary Graduate School of Engineering Sciences Kyushu University
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Kanemasa Shuji
Research Institute of Industrial Science, Kyushu University
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Kanemasa Shuji
Research Institute of Industrial Science, and Department of Molecular Science and Technology, Interdisciplinary Graduate School of Engineering Science, Kyushu University
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