Efficient construction of the core framework of lysidicin A via three Claisen rearrangements including a cascade reaction

Yusuke Ogura, Hidenori Watanabe

研究成果: Article査読

2 被引用数 (Scopus)

抄録

A model compound (6) with the core skeleton of lysidicin A was synthesized as a racemate. The key step (8→7) includes three Claisen rearrangements of the triether with phloroglucinols; two of which rearranged in a cascade manner and the other was a simple rearrangement. This one-pot reaction enabled the introduction of three phloroglucinol units at the correct positions and makes the synthetic approach significantly efficient.

本文言語English
ページ(範囲)3294-3296
ページ数3
ジャーナルTetrahedron Letters
51
25
DOI
出版ステータスPublished - 2010 6月 23
外部発表はい

ASJC Scopus subject areas

  • 生化学
  • 創薬
  • 有機化学

フィンガープリント

「Efficient construction of the core framework of lysidicin A via three Claisen rearrangements including a cascade reaction」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル