Cobaltaelectro-catalyzed C–H acyloxylation of aromatic and vinylic amide derivatives at room temperature

Herein, we report a mild and efficient cobalt-catalyzed electrochemical method for the regioselective C-H acyloxylation of aromatic and vinylic amides, utilizing 8-aminoquinoline as the directing group. Notably, this protocol requires no stoichiometric oxidants and operates at room temperature in an undivided cell setup, providing sustainable access to a diverse set of <i>ortho</i>-acyloxylated products with broad functional group tolerance.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc04394h
Citations
1
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Cobaltaelectro-catalyzed C–H acyloxylation of aromatic and vinylic amide derivatives at room temperature

Ruzal Sitdikov, Oscar Verho, Pavlo Nikolaienko
1 citations
Chemical Communications
Oxidative Organic Chemistry Reactions
0.94
article

Cobaltaelectro-catalyzed C–H acyloxylation of aromatic and vinylic amide derivatives at room temperature

Ruzal Sitdikov, Oscar Verho, Pavlo Nikolaienko
article en
1 citations

Abstract

Herein, we report a mild and efficient cobalt-catalyzed electrochemical method for the regioselective C-H acyloxylation of aromatic and vinylic amides, utilizing 8-aminoquinoline as the directing group. Notably, this protocol requires no stoichiometric oxidants and operates at room temperature in an undivided cell setup, providing sustainable access to a diverse set of <i>ortho</i>-acyloxylated products with broad functional group tolerance.

Chemical CommunicationsVol. 61(87)
Uppsala University (SE), Helmholtz Institute Erlangen-Nürnberg (DE)
Svenska Forskningsrådet Formas, Vetenskapsrådet, Magnus Bergvalls Stiftelse
Openalex Percentile: Top 21%
Oxidative Organic Chemistry Reactions
0.94
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