Electrochemical Dehydrocarboxylation of Alcohols Mediated by Cu <sub>0.5</sub> Ni <sub>0.5</sub> -LDH

Oxidation of primary alcohols to produce the corresponding carboxylic acids is a fundamental reaction in organic synthesis. In this article, we report a process for the oxidation of primary alcohols using chemically modified electrodes. This is characterized as a green, mild, oxidant-free, and easy-to-operate process with high isolation yields and good functional group tolerance. A series of controlled experiments demonstrate the reaction mechanism.

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Publication Details

Journal
Organic Letters
Published
2025-11-10
DOI
https://doi.org/10.1021/acs.orglett.5c03569
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Electrochemical Dehydrocarboxylation of Alcohols Mediated by Cu 0.5 Ni 0.5 -LDH

Lin‐Bao Zhang, Weisi Guo, Hongtao Gao, Wenlong Yang et al.
Organic Letters
Oxidative Organic Chemistry Reactions
article

Electrochemical Dehydrocarboxylation of Alcohols Mediated by Cu 0.5 Ni 0.5 -LDH

Lin‐Bao Zhang, Weisi Guo, Hongtao Gao, Wenlong Yang, Ming Li, Xinyu Zhang, Jiaxiu Liu, Fengjuan Guo
article en

Abstract

Oxidation of primary alcohols to produce the corresponding carboxylic acids is a fundamental reaction in organic synthesis. In this article, we report a process for the oxidation of primary alcohols using chemically modified electrodes. This is characterized as a green, mild, oxidant-free, and easy-to-operate process with high isolation yields and good functional group tolerance. A series of controlled experiments demonstrate the reaction mechanism.

Organic LettersVol. 27(46)
Qingdao University of Science and Technology (CN)
Openalex Percentile: Top 75%
Oxidative Organic Chemistry Reactions
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