eAmidation: An Electrochemical Amidation of Aldehydes via the Oxidation of <i>N</i> ‐Aryl Hydrazones

In recent years, the use of electrochemistry has emerged as a powerful yet sustainable means of enabling key transformations. Amidation is one of the most frequently executed transformations in synthetic chemistry, and using an electrochemical approach, the current study has demonstrated the synthesis of amides from aldehydes and amines. Mechanistic work indicates that the reaction proceeds via the oxidation of an intermediate hydrazone to generate an acyl diazene as the acylating species. The protocol developed has enabled the synthesis of a broad range of amides, including access to pharmaceutically relevant products, directly from aldehydes without recourse for hazardous chemical oxidants and activating agents.

Authors

Institutions

Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-06-12
DOI
https://doi.org/10.1002/adsc.9587
Citations
3
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
2.42

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

eAmidation: An Electrochemical Amidation of Aldehydes via the Oxidation of N ‐Aryl Hydrazones

James D. F. Thompson, Craig Jamieson, Liming Chen
3 citations
Advanced Synthesis & Catalysis
Chemical Synthesis and Analysis
2.42
article

eAmidation: An Electrochemical Amidation of Aldehydes via the Oxidation of N ‐Aryl Hydrazones

James D. F. Thompson, Craig Jamieson, Liming Chen
article en
3 citations

Abstract

In recent years, the use of electrochemistry has emerged as a powerful yet sustainable means of enabling key transformations. Amidation is one of the most frequently executed transformations in synthetic chemistry, and using an electrochemical approach, the current study has demonstrated the synthesis of amides from aldehydes and amines. Mechanistic work indicates that the reaction proceeds via the oxidation of an intermediate hydrazone to generate an acyl diazene as the acylating species. The protocol developed has enabled the synthesis of a broad range of amides, including access to pharmaceutically relevant products, directly from aldehydes without recourse for hazardous chemical oxidants and activating agents.

Advanced Synthesis & CatalysisVol. 367(14)
University of Strathclyde (GB), Age UK (GB)
Engineering and Physical Sciences Research Council
Openalex Percentile: Top 11%
Chemical Synthesis and Analysis
2.42
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.