(+/-) アクチノフィル酸の総合成
Connor L Martin1, Larry E Overman, Jason M Rohde
1Department of Chemistry, 1102 Natural Sciences II, University of California, Irvine, California 92697-2025, USA.
Journal of the American Chemical Society
|May 22, 2008
まとめ
研究者らは,アクチノフィル酸の最初の完全合成を報告した. 鍵となるステップは,酸化結合とアザ・コップ・マニッヒの再編成による自然産物の構築であった.
科学分野:
- 有機化学 オーガニック・ケミストリー
- 自然製品合成 自然製品合成
背景:
- アクチノフィル酸は,ユニークなリングシステムを持つ複雑な天然製品です.
- アクチノフィル酸への以前の合成経路は欠けていた.
研究 の 目的:
- (+/-) -アクチノフィル酸の最初の完全合成を達成するために.
- 効率的で簡潔な合成戦略を開発する.
主な方法:
- ケトンとマロンエステルエノラートの分子内酸化結合を用いた.
- Aza-Cope-Mannichの再編成を使用して,コア構造を組み立てました.
- 標的分子をdi-tert-butyl malonateから合成した.
主要な成果:
- (+/-) アクチノフィル酸の最初の完全合成を成功裏に完了しました.
- 8%の総収益率を達成しました.
- 合成には,わずか7つの分離された中間物質を含む簡潔な配列が含まれていました.
結論:
- 開発された合成経路は,アクチノフィル酸へのアクセスを提供します.
- 鍵となる反応である酸化結合とアザ・コップ・マニッヒの再編成は,自然産物の複雑な構造を構築するのに有効である.
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