ヘルクリンBとCの総合合成
Joshua B Cox1, Aoi Kimishima1, John L Wood1
1Department of Chemistry and Biochemistry , Baylor University , One Bear Place 97348 , Waco , Texas 76798 , United States.
Journal of the American Chemical Society
|December 19, 2018
まとめ
複合的な天然製品である (-) - ヘルクリンBと (+) - ヘルクリンCの全合成が達成されました. これらの多段階合成において,重要なオクサゾリンの減少により,効率的なピペラジン環の構築が可能になった.
科学分野:
- 有機化学
- 自然製品合成
背景:
- (-) - ヘルクリンBは潜在的生物学的活性を持つ天然製品です.
- 関連化合物の構造の解明は進行中です.
研究 の 目的:
- (-) - ヘルクリンBの全合成を記述する.
- 新たに特定された同類物質 (+) - ヘルクリンCの最初の合成を報告する.
主な方法:
- 多段階の有機合成です
- 鍵となるステップは,ピペラジンの核形成のためのオクサゾリンの減少です.
主要な成果:
- 14段階の (-) - ヘルクリンBの完全な合成が成功しました.
- (+) - ヘルクリンCを13ステップで初めて合成する.
- 戦略的なオクサゾリンの減少をピペラジン構造で示した.
結論:
- 記述された合成経路は,ヘルクリンアルカロイドへのアクセスを提供します.
- 効率的なピペラジン環形成には,重要な減少段階が不可欠です.
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