Journal
CHEMICAL COMMUNICATIONS
Volume 59, Issue 40, Pages 6092-6095Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cc00605k
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This study describes a photoredox-catalyzed arylative radical cascade reaction involving N-acryloyl-2-arylbenzoimidazoles and diaryliodonium triflates, leading to the formation of a diverse range of pharmaceutically important arylated-benzimidazo[2,1-a]isoquinolin-6(5H)-ones. Importantly, the synthesized benzimidazoisoquinolinones are easily manipulated for further synthesis, allowing efficient access to benzimidazole-fused polycyclic heterocycles.
A photoredox-catalyzed arylative radical cascade involving N-acryloyl-2-arylbenzoimidazoles and diaryliodonium triflates leading to the formation of a broad array of pharmaceutically important arylated-benzimidazo[2,1-a]isoquinolin-6(5H)-ones is described. Importantly, the synthesized benzimidazoisoquinolinones are amenable for further synthetic manipulation and allowed efficient access to benzimidazo-fused polycyclic heterocycles.
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