Nickel-Catalyzed Carbonylation Reaction of Aryl <i>N</i>-Tosylaziridines with Arylboronic Acids toward β-Amino Ketones

A novel nickel-catalyzed carbonylation reaction of aryl N-tosylaziridines with arylboronic acids has been explored for the synthesis of β-amino ketones. By using formic acid as the CO source, a variety of β-amino ketones were obtained in moderate to excellent yields. This approach features high regioselectivity, good functional group tolerance, and a CO gas-free operation. It provides a good supplement for the ring-opening transformation of aziridines through a nickel-catalyzed radical carbonylation process.

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Publication Details

Journal
ACS Catalysis
Published
2025-07-18
DOI
https://doi.org/10.1021/acscatal.5c03618
Citations
5
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
4.68
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article

Nickel-Catalyzed Carbonylation Reaction of Aryl N-Tosylaziridines with Arylboronic Acids toward β-Amino Ketones

Xiao‐Feng Wu, Pengfei Ji, Chen-Yang Hou, Tong Li et al.
5 citations
ACS Catalysis
Synthesis and Catalytic Reactions
4.68
article

Nickel-Catalyzed Carbonylation Reaction of Aryl N-Tosylaziridines with Arylboronic Acids toward β-Amino Ketones

Xiao‐Feng Wu, Pengfei Ji, Chen-Yang Hou, Tong Li, Xinxin Qi, Boyu Yao
article en
5 citations

Abstract

A novel nickel-catalyzed carbonylation reaction of aryl N-tosylaziridines with arylboronic acids has been explored for the synthesis of β-amino ketones. By using formic acid as the CO source, a variety of β-amino ketones were obtained in moderate to excellent yields. This approach features high regioselectivity, good functional group tolerance, and a CO gas-free operation. It provides a good supplement for the ring-opening transformation of aziridines through a nickel-catalyzed radical carbonylation process.

ACS CatalysisVol. 15(15)
Zhejiang Sci-Tech University (CN), Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Leibniz Institute for Catalysis (DE), Ingenierie des Materiaux polymeres (FR), Dalian National Laboratory for Clean Energy (CN), Interface (United Kingdom) (GB)
Openalex Percentile: Top 5%
Synthesis and Catalytic Reactions
4.68
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