Iron-Catalyzed Direct Aldehyde-to-Carbene Conversion via Ketyl Radicals

Carbene chemistry is at the forefront of modern synthetic methodology due to its ability to unlock a plethora of chemical transformations. Traditional reliance on diazo compounds, while effective, is hindered by their inherent instability, toxicity, and limited functional group tolerance. Recent advances have explored alternative carbene precursors, yet the direct catalytic generation of carbenes from aldehydes remains underexplored. Here, we report a mild iron-catalyzed carbene transfer protocol that directly accesses carbene intermediates from aldehydes via a ketyl radical mechanism. This method obviates the need for prefunctionalized precursors, enabling the synthesis of diverse functionalized cyclopropanes with good efficiency and functional group compatibility. Mechanistic investigations, including radical trapping, σ-bond insertion, and olefin metathesis experiments, corroborate the intermediacy of ketyl radicals and iron carbenes. This work expands the synthetic utility of aldehydes, offering a robust platform for carbene transfer reactions and the synthesis of valuable cyclopropane scaffolds.

Authors

Institutions

Publication Details

Journal
ACS Catalysis
Published
2025-11-03
DOI
https://doi.org/10.1021/acscatal.5c06888
Citations
4
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
3.74
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Iron-Catalyzed Direct Aldehyde-to-Carbene Conversion via Ketyl Radicals

Zhaobin Wang, Haigen Shen, Xiaoyu Lin
4 citations
ACS Catalysis
Cyclopropane Reaction Mechanisms
3.74
article

Iron-Catalyzed Direct Aldehyde-to-Carbene Conversion via Ketyl Radicals

Zhaobin Wang, Haigen Shen, Xiaoyu Lin
article en
4 citations

Abstract

Carbene chemistry is at the forefront of modern synthetic methodology due to its ability to unlock a plethora of chemical transformations. Traditional reliance on diazo compounds, while effective, is hindered by their inherent instability, toxicity, and limited functional group tolerance. Recent advances have explored alternative carbene precursors, yet the direct catalytic generation of carbenes from aldehydes remains underexplored. Here, we report a mild iron-catalyzed carbene transfer protocol that directly accesses carbene intermediates from aldehydes via a ketyl radical mechanism. This method obviates the need for prefunctionalized precursors, enabling the synthesis of diverse functionalized cyclopropanes with good efficiency and functional group compatibility. Mechanistic investigations, including radical trapping, σ-bond insertion, and olefin metathesis experiments, corroborate the intermediacy of ketyl radicals and iron carbenes. This work expands the synthetic utility of aldehydes, offering a robust platform for carbene transfer reactions and the synthesis of valuable cyclopropane scaffolds.

ACS CatalysisVol. 15(22)
Westlake University (CN), Institute for Advanced Study (DE), Institute of Natural Science (KP), Chemical Synthesis Lab (SG), Nanjing University (CN)
Openalex Percentile: Top 7%
Cyclopropane Reaction Mechanisms
3.74
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.