Communication to the Editor : Oxidative Rearrangement of Cyclobutanone Derived N,O-Ketals Leading to Pyrrolidone Derivatives

  • Murai Kenichi
    Graduate School of Pharmaceutical Sciences, Osaka University
  • Endo Daisuke
    Graduate School of Pharmaceutical Sciences, Osaka University
  • Kawashita Norihito
    Graduate School of Pharmaceutical Sciences, Osaka University Research Institute for Microbial Diseases, Osaka University
  • Takagi Tatsuya
    Graduate School of Pharmaceutical Sciences, Osaka University Research Institute for Microbial Diseases, Osaka University
  • Fujioka Hiromichi
    Graduate School of Pharmaceutical Sciences, Osaka University

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タイトル別名
  • Oxidative Rearrangement of Cyclobutanone Derived <i>N</i>,<i>O</i>-Ketals Leading to Pyrrolidone Derivatives

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A halogen-induced oxidative rearrangement of N,O-ketals prepared from cyclobutanones, leading to pyrrolidone derivatives, is developed. The reaction proceeds via an iminium ether intermediate and, depending on the reaction medium, two types of pyrrolidone derivative, containing a halogen atom or hydroxyl group, can be obtained.

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