Metal- and CO-Free Carbonylation of Alkyl Iodides
We report a new method for the carbonylation of alkyl iodides under photochemical conditions. The process relies on a simple aryl formate reagent, synthesized in one step from readily available chemicals and capable of releasing CO along with a phenolate species in the presence of a mild base. The photoactivity of this phenolate is harnessed to activate alkyl iodides via single-electron transfer and generate alkyl radicals that add to CO and ultimately offer access to carboxylic acids and amides. This new, user-friendly procedure overcomes the typical need for CO gas and/or metal catalysts in carbonylation chemistry while being highly efficient and versatile to accommodate a variety of functional groups.
Authors
- Emilien Le Saux (ORCID: https://orcid.org/0000-0003-1887-6687)
- Matthew Mathis
- Bill Morandi (ORCID: https://orcid.org/0000-0003-3968-1424)
- Giorgia Panizzolo
Institutions
- ETH Zurich (CH)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-10-16
- DOI
- https://doi.org/10.1021/jacs.5c13505
- Citations
- 1
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.70