Homogeneous copper-catalyzed aerobic oxidation of alcohols and aldehydes: mechanistic insights and recent advances

Copper-catalyzed aerobic oxidation of alcohols and aldehydes has become a key transformation for the sustainable synthesis of carbonyl compounds, combining high efficiency with the use of molecular oxygen as a benign terminal oxidant. Owing to its earth-abundance, low cost, low toxicity, and versatile redox properties, copper offers a compelling alternative to traditional noble metal catalysts and stoichiometric oxidation methods. This review highlights the evolution of copper-catalyzed aerobic oxidation of alcohols, emphasizing two distinct mechanistic regimes: nitroxyl radical-mediated systems and nitroxyl-free pathways, in which copper–ligand complexes directly promote dioxygen activation and substrate oxidation. Methods for conversion of aldehydes to carboxylic acids were also discussed. Apart from historical overview of the considered protocols, recent advances in the field were deliberated. Despite significant progress, the development of simpler, mediator-free catalytic systems based on readily available reagents remains a central challenge and a promising direction for future research.

Authors

Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2026-09-29
DOI
https://doi.org/10.3762/bjoc.22.107
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Homogeneous copper-catalyzed aerobic oxidation of alcohols and aldehydes: mechanistic insights and recent advances

Svilen Plamenov Simeonov, Hristo Petkov
Beilstein Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
article

Homogeneous copper-catalyzed aerobic oxidation of alcohols and aldehydes: mechanistic insights and recent advances

Svilen Plamenov Simeonov, Hristo Petkov
article en

Abstract

Copper-catalyzed aerobic oxidation of alcohols and aldehydes has become a key transformation for the sustainable synthesis of carbonyl compounds, combining high efficiency with the use of molecular oxygen as a benign terminal oxidant. Owing to its earth-abundance, low cost, low toxicity, and versatile redox properties, copper offers a compelling alternative to traditional noble metal catalysts and stoichiometric oxidation methods. This review highlights the evolution of copper-catalyzed aerobic oxidation of alcohols, emphasizing two distinct mechanistic regimes: nitroxyl radical-mediated systems and nitroxyl-free pathways, in which copper–ligand complexes directly promote dioxygen activation and substrate oxidation. Methods for conversion of aldehydes to carboxylic acids were also discussed. Apart from historical overview of the considered protocols, recent advances in the field were deliberated. Despite significant progress, the development of simpler, mediator-free catalytic systems based on readily available reagents remains a central challenge and a promising direction for future research.

Beilstein Journal of Organic ChemistryVol. 22
Openalex Percentile: Top 22%
Oxidative Organic Chemistry Reactions
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.

Homogeneous copper-catalyzed aerobic oxidation of alcohols and aldehydes: mechanistic insights and recent advances — Svilen Plamenov Simeonov, Hristo Petkov · Beilstein Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS