Photoinduced N-Heterocyclic Nitrenium-Catalyzed Single Electron Reduction of Acyl Fluorides for Phenanthridine Synthesis

Acyl fluorides are versatile reagents in organic synthesis. However, there is no precedent to employ acyl fluorides as acyl radical precursors. We herein report an N-heterocyclic nitrenium iodide salt catalyzed photoreduction of acyl fluorides to produce acyl radicals, which could react with 2-isocyanobiaryls to afford various carbonyl phenanthridines.

Automated summary

In this study, we reported a method for the photoreduction of acyl fluorides using N-heterocyclic nitrenium iodide salt as catalyst to generate acyl radicals, which can react with 2-isocyanobiaryls to form various carbonyl phenanthridines.