Electrooxidative Ni‐Catalyzed Decarboxylation of Arylacetic Acids Towards the Synthesis of Carbonyls under Air Conditions

After systematic realization of decarboxylative functionalization of carboxylic acids under heating conditions in our group, we herein reported an electrochemical method for Ni-catalyzed decarboxylative oxygenation of arylacetic acids under open air conditions. The protocol provided corresponding carbonyls including aldehydes and ketones in moderate to satisfactory yields with good functional group tolerance, furthermore, the practicability and advantage of the method was highlighted through Ni-catalyzed oxidative decarboxylation of carboxylic acid-containing drugs and preformation of scalable transformation. Mechanistic studies demonstrated that the possible involvement of free radical intermediate in the conversion.

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Publication Details

Journal
Chemistry - A European Journal
Published
2024-09-16
DOI
https://doi.org/10.1002/chem.202403077
Citations
4
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
1.00

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article

Electrooxidative Ni‐Catalyzed Decarboxylation of Arylacetic Acids Towards the Synthesis of Carbonyls under Air Conditions

Shengmei Guo, Zhengjiang Fu, Hu Cai, Junhua Zeng et al.
4 citations
Chemistry - A European Journal
Oxidative Organic Chemistry Reactions
1.00
article

Electrooxidative Ni‐Catalyzed Decarboxylation of Arylacetic Acids Towards the Synthesis of Carbonyls under Air Conditions

Shengmei Guo, Zhengjiang Fu, Hu Cai, Junhua Zeng, Cheng Xiong
article en
4 citations

Abstract

After systematic realization of decarboxylative functionalization of carboxylic acids under heating conditions in our group, we herein reported an electrochemical method for Ni-catalyzed decarboxylative oxygenation of arylacetic acids under open air conditions. The protocol provided corresponding carbonyls including aldehydes and ketones in moderate to satisfactory yields with good functional group tolerance, furthermore, the practicability and advantage of the method was highlighted through Ni-catalyzed oxidative decarboxylation of carboxylic acid-containing drugs and preformation of scalable transformation. Mechanistic studies demonstrated that the possible involvement of free radical intermediate in the conversion.

Chemistry - A European JournalVol. 30(69)
Nanchang University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangxi Province
Clean water and sanitation
Openalex Percentile: Top 27%
Oxidative Organic Chemistry Reactions
1.00
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