# Photoredox-catalyzed arylation of isonitriles by diaryliodonium salts towards benzamides

**Authors:** Nadezhda M Metalnikova, Nikita S Antonkin, Tuan K Nguyen, Natalia S Soldatova, Alexander V Nyuchev, Mikhail A Kinzhalov, Pavel S Postnikov

PMC · DOI: 10.3762/bjoc.21.110 · Beilstein Journal of Organic Chemistry · 2025-07-21

## TL;DR

This paper introduces a new method for making benzamides using light-driven reactions with isonitriles and diaryliodonium salts.

## Contribution

The first reported use of photoredox catalysis for arylation of isonitriles with diaryliodonium salts to form benzamides.

## Key findings

- Arylation of isonitriles using diaryliodonium salts under photoredox conditions produces benzamides.
- The method works with both symmetric and unsymmetric diaryliodonium salts under mild conditions.
- A plausible reaction mechanism and selectivity in aryl transfer were investigated.

## Abstract

The arylation of isonitriles by diaryliodonium salts under photoredox conditions has been proposed for the first time. The suggested procedure allows preparing a broad range of benzamides using both symmetric and unsymmetric diaryliodonium salts under mild conditions. A plausible mechanism for the reaction and the selectivity of aryl transfer (in case of unsymmetrical iodonium salts) were studied.

## Full-text entities

- **Chemicals:** Photoredox (-), benzamides (MESH:D001549)

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12302481/full.md

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Source: https://tomesphere.com/paper/PMC12302481