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I 2 /FeCl 3 -Catalyzed Domino Reaction of Aurones with Enamino Esters for the Synthesis of Highly Functionalized Pyrroles.

Hui XuMing-Jun LiHong ChenFei-Hong HuangQi-Yue ZhuGuan-Wu WangZe Zhang
Published in: Organic letters (2022)
A novel and efficient I 2 /FeCl 3 -catalyzed domino reaction of aurones with enamino esters via Michael addition, iodination, intramolecular nucleophilic substitution, and spiro ring opening processes has been developed, affording a vast variety of polysubstituted pyrroles in moderate to excellent yields. This protocol features mild reaction conditions, broad substrate scope, high atom economy and efficiency, and feasibility for large-scale synthesis. A plausible mechanism for the pyrrole synthesis is proposed.
Keyphrases
  • room temperature
  • randomized controlled trial
  • molecular dynamics
  • high intensity
  • liquid chromatography