Paired Electrolysis-Promoted Ni-Catalyzed Decarboxylative Cross-Couplings of Potassium Malonate Monoesters with Aryl Bromides

We report a paired electrolysis-promoted Ni-catalyzed decarboxylative cross-coupling of aryl bromides with potassium malonate monoesters. Carried out in an undivided electrolytic cell under mild reaction conditions, this strategy exhibits broad compatibility with a wide range of aryl/heteroaryl and vinyl bromides, offering a practical and efficient protocol for the synthesis of α-aryl esters.

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Publication Details

Journal
Organic Letters
Published
2026-03-16
DOI
https://doi.org/10.1021/acs.orglett.6c00805
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
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article

Paired Electrolysis-Promoted Ni-Catalyzed Decarboxylative Cross-Couplings of Potassium Malonate Monoesters with Aryl Bromides

Jinzhong Yao, S. H. Zhang, Shuai Lv, Hongwei Zhou
Organic Letters
Catalytic Cross-Coupling Reactions
article

Paired Electrolysis-Promoted Ni-Catalyzed Decarboxylative Cross-Couplings of Potassium Malonate Monoesters with Aryl Bromides

Jinzhong Yao, S. H. Zhang, Shuai Lv, Hongwei Zhou
article en

Abstract

We report a paired electrolysis-promoted Ni-catalyzed decarboxylative cross-coupling of aryl bromides with potassium malonate monoesters. Carried out in an undivided electrolytic cell under mild reaction conditions, this strategy exhibits broad compatibility with a wide range of aryl/heteroaryl and vinyl bromides, offering a practical and efficient protocol for the synthesis of α-aryl esters.

Organic LettersVol. 28(12)
Jiaxing University (CN)
Openalex Percentile: Top 20%
Catalytic Cross-Coupling Reactions
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