Electrochemical Oxidative Carbonylation/Coupling Reaction using Anode to Oxidize the Trasition‐Metal‐Catalyst and Substrate

Abstract We reported an electrochemical oxidative carbonylation of N ‐phenylpyridin‐2‐amine derivatives under mild condtions without an external oxidant. Our approach demonstrated a novel electrochemical oxidative carbonylation reaction mode in which the simultaneous reaction of catalyst and substrate with the anode has been developed. Furthermore, an electrochemical C−H activation for the synthesis of cyclized pyridinium ion has also been realized. Mechanistic investigations suggested that the process involved a “Pd II /Pd III /Pd I /Pd II ” catalytic cycle, and H 2 was generated at the cathode.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-01-27
DOI
https://doi.org/10.1002/adsc.202401454
Citations
1
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.54
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article

Electrochemical Oxidative Carbonylation/Coupling Reaction using Anode to Oxidize the Trasition‐Metal‐Catalyst and Substrate

Huimin Li, Longqiang Zhao, Qingge Zhao, Mengyu Peng
1 citations
Advanced Synthesis & Catalysis
Asymmetric Hydrogenation and Catalysis
0.54
article

Electrochemical Oxidative Carbonylation/Coupling Reaction using Anode to Oxidize the Trasition‐Metal‐Catalyst and Substrate

Huimin Li, Longqiang Zhao, Qingge Zhao, Mengyu Peng
article en
1 citations

Abstract

Abstract We reported an electrochemical oxidative carbonylation of N ‐phenylpyridin‐2‐amine derivatives under mild condtions without an external oxidant. Our approach demonstrated a novel electrochemical oxidative carbonylation reaction mode in which the simultaneous reaction of catalyst and substrate with the anode has been developed. Furthermore, an electrochemical C−H activation for the synthesis of cyclized pyridinium ion has also been realized. Mechanistic investigations suggested that the process involved a “Pd II /Pd III /Pd I /Pd II ” catalytic cycle, and H 2 was generated at the cathode.

Advanced Synthesis & CatalysisVol. 367(12)
Guilin University of Technology (CN)
Openalex Percentile: Top 40%
Asymmetric Hydrogenation and Catalysis
0.54
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