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Photoredox-Catalyzed Cascade Reactions Involving Aryl Radical: Total Synthesis of (±)-Norascyronone A and (±)-Eudesmol.

Ze-Jun XuXu-Yuan LiuMing-Zhu ZhuYu-Liang XuYue YuHai-Ruo XuAi-Xia ChengHong-Xiang Lou
Published in: Organic letters (2021)
Herein, we have developed two types of photoredox-catalyzed cascade reactions using diaryliodonium salts for the concise synthesis of norascyronone A and β-eudesmol. A rationally designed photoredox-catalyzed arylation/cyclization/Friedel-Crafts cascade reaction of enone was exploited to generate the norascyronone polycyclic skeleton. A visible-light-induced radical cyclization/acyloxy-migration reaction was explored to forge the decalin skeleton of eudesmol, and mechanistic studies indicated the reaction was initiated by one-electron oxidation of the enol ester.
Keyphrases
  • visible light
  • room temperature
  • electron transfer
  • ionic liquid
  • hydrogen peroxide
  • nitric oxide