Formate Salt as a Bifunctional Reagent for Hydroxylation and Carbonylation Reactions Under Photochemically Driven Nickel Catalysis
In this study, we disclose for the first time that formate salt can be used as a bifunctional reagent for the synthesis of phenol derivatives and as a CO source for carbonylative cross-coupling processes using the COware gas reactor under activation free conditions. Key to this success is the in-situ synthesis of aryl formate via an unprecedented nickel/organophotocatalyst system under blue LED irradiation. This developed system demonstrated high applicability to various aryl iodide substrates for synthesizing phenol derivatives. Moreover, the generated CO could be utilized in a range of carbonylative C-heteroatom and C-C processes. Notably, commercially available H<sup>13</sup>COONa salt can serve as a bifunctional reagent for both synthesizing phenols and generating <sup>13</sup>CO.
Authors
- Anis Tlili (ORCID: https://orcid.org/0000-0002-3058-2043)
- Yi Yang (ORCID: https://orcid.org/0000-0001-6057-3378)
- Martin Nielsen (ORCID: https://orcid.org/0000-0002-3170-1198)
- Timothe Guerin
- Jiangshang Su
Institutions
- Université Claude Bernard Lyon 1 (FR)
- Centre National de la Recherche Scientifique (FR)
- Institut de Chimie et Biochimie Moléculaires et Supramoléculaires (FR)
- Laboratoire Hydrazines et Composés Energétiques Polyazotés (FR)
- Technical University of Denmark (DK)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2024-08-31
- DOI
- https://doi.org/10.1002/chem.202403221
- Citations
- 1
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.25
Funders
- Villum Fonden
- China Scholarship Council
- Centre National de la Recherche Scientifique