Formate Salt as a Bifunctional Reagent for Hydroxylation and Carbonylation Reactions Under Photochemically Driven Nickel Catalysis - Institut de Chimie et Biochimie Moléculaires et Supramoléculaires
Article Dans Une Revue Chemistry - A European Journal Année : 2024

Formate Salt as a Bifunctional Reagent for Hydroxylation and Carbonylation Reactions Under Photochemically Driven Nickel Catalysis

Résumé

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 13 COONa salt can serve as a bifunctional reagent for both synthesizing phenols and generating 13 CO.

Domaines

Chimie
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vendredi 28 février 2025
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vendredi 28 février 2025
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Dates et versions

hal-04777076 , version 1 (12-11-2024)

Identifiants

Citer

Yi Yang, Junping Su, Timothe Guerin, Martin Nielsen, Anis Tlili. Formate Salt as a Bifunctional Reagent for Hydroxylation and Carbonylation Reactions Under Photochemically Driven Nickel Catalysis. Chemistry - A European Journal, 2024, pp.e202403221. ⟨10.1002/chem.202403221⟩. ⟨hal-04777076⟩
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