The Cycloaddition of N,.ALPHA.-Diarylnitrones and Substituted p-Benzoquinones.

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概要

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• <I>N</I>,α-Diarylnitrones reacted with 2,5- or 2,6-dialkyl-<I>p</I>-benzoquinones at their C=C bond regioselectively to give fused isoxazolidine cycloadducts. These cycloadducts were proved to undergo retrocycloaddition. <I>p</I>-Benzoquinones having electron-withdrawing substituents did not give any cycloadduct.

• 公益社団法人 日本化学会の論文

著者

• Inoue Yukihiko

  The Institute of Industrial Science, The University of Tokyo

• Shiraishi Shinsaku

  The Institute of Industrial Science, The University of Tokyo

• Imamura Kiyoshi

  The Institute of Industrial Science, The University of Tokyo

関連論文

• The Cycloaddition of N,.ALPHA.-Diarylnitrones and Substituted p-Benzoquinones.

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