Asymmetric Total Synthesis of (−)-Scabronine G via Intramolecular Double Michael Reaction and Prins Cyclization

  • Naoki Kanoh
    Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan
  • Kohei Sakanishi
    Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan
  • Emiko Iimori
    Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan
  • Ken’ichi Nishimura
    Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan
  • Yoshiharu Iwabuchi
    Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan

書誌事項

公開日
2011-05-06
資源種別
journal article
DOI
  • 10.1021/ol200873y
公開者
American Chemical Society (ACS)

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説明

The enantioselective total synthesis of (-)-scabronine G is described. The key features of the present synthesis include the construction of a 5-6 ring system containing two quaternary carbon centers via a diastereoselective intramolecular double Michael reaction and the formation of a seven-membered ring using a Prins cyclization.

収録刊行物

  • Organic Letters

    Organic Letters 13 (11), 2864-2867, 2011-05-06

    American Chemical Society (ACS)

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