Electrochemically Driven Nickel-Catalyzed Synthesis of Aryl Alkyl Ketones by the Cross-Coupling of Carboxylic Esters with Alkylpyridinium Salts

An electrochemical Ni-catalyzed reductive cross-coupling of arylcarboxylic esters with alkylpyridinium salts has been developed. Various aryl alkyl ketones are obtained in good to excellent yields (up to 86% yield). The reaction tolerated a variety of primary alkylpyridinium salts, including substrates with protic functional groups and derivatives of bioactive molecules. This method exhibits several synthetic advantages, including high efficiency (reaction time of 1.5 h), the use of easily available alkylpyridinium salts (dual roles as the alkyl source and electrolyte), a convenient procedure (undivided cell), and a wide substrate scope (47 examples). This route provides a novel and efficient method for the synthesis of aryl ketones.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-08-29
DOI
https://doi.org/10.1021/acs.joc.5c01714
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94

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article

Electrochemically Driven Nickel-Catalyzed Synthesis of Aryl Alkyl Ketones by the Cross-Coupling of Carboxylic Esters with Alkylpyridinium Salts

Qi-Ying Zhang, Qi‐Liang Yang, Shikun Li, Hai‐Ming Guo et al.
1 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.94
article

Electrochemically Driven Nickel-Catalyzed Synthesis of Aryl Alkyl Ketones by the Cross-Coupling of Carboxylic Esters with Alkylpyridinium Salts

Qi-Ying Zhang, Qi‐Liang Yang, Shikun Li, Hai‐Ming Guo, Jing Ma
article en
1 citations

Abstract

An electrochemical Ni-catalyzed reductive cross-coupling of arylcarboxylic esters with alkylpyridinium salts has been developed. Various aryl alkyl ketones are obtained in good to excellent yields (up to 86% yield). The reaction tolerated a variety of primary alkylpyridinium salts, including substrates with protic functional groups and derivatives of bioactive molecules. This method exhibits several synthetic advantages, including high efficiency (reaction time of 1.5 h), the use of easily available alkylpyridinium salts (dual roles as the alkyl source and electrolyte), a convenient procedure (undivided cell), and a wide substrate scope (47 examples). This route provides a novel and efficient method for the synthesis of aryl ketones.

The Journal of Organic ChemistryVol. 90(36)
Henan Normal University (CN)
National Natural Science Foundation of China, Henan Key Laboratory of Organic Functional Molecules and Drug Innovation, Henan Provincial Science and Technology Research Project
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
0.94
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Electrochemically Driven Nickel-Catalyzed Synthesis of Aryl Alkyl Ketones by the Cross-Coupling of Carboxylic Esters with Alkylpyridinium Salts — Qi-Ying Zhang, Qi‐Liang Yang, et al. · The Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS