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.

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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

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article

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

Anis Tlili, Yi Yang, Martin Nielsen, Timothe Guerin et al.
1 citations
Chemistry - A European Journal
Radical Photochemical Reactions
0.25
article

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

Anis Tlili, Yi Yang, Martin Nielsen, Timothe Guerin, Jiangshang Su
article en
1 citations

Abstract

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.

Chemistry - A European JournalVol. 30(65)
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)
Villum Fonden, China Scholarship Council, Centre National de la Recherche Scientifique
Clean water and sanitation
Openalex Percentile: Top 49%
Radical Photochemical Reactions
0.25
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