Visible-Light-Induced 4CzIPN-Catalyzed Alkylamination of Alkenes via Cyclobutanone Oxime Esters and Anilines

We disclosed an organophotoredox-catalyzed three-component oxidative radical-polar crossover strategy for constructing 1,2-alkylamination products. Cycloketone oxime derivatives were used as cyanoalkyl radical precursors and anilines were used as the nucleophiles. This facile protocol shows a good reaction yield and broad substrate scope.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-22
DOI
https://doi.org/10.1021/acs.joc.4c02172
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87

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article

Visible-Light-Induced 4CzIPN-Catalyzed Alkylamination of Alkenes via Cyclobutanone Oxime Esters and Anilines

Li Guo, Zeyu Tian, Jianghong Liu, Tianle Huang et al.
2 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
1.87
article

Visible-Light-Induced 4CzIPN-Catalyzed Alkylamination of Alkenes via Cyclobutanone Oxime Esters and Anilines

Li Guo, Zeyu Tian, Jianghong Liu, Tianle Huang, Zhongzhen Yang, Yong Wu, Hai Li, Zhen-Ye Wu
article en
2 citations

Abstract

We disclosed an organophotoredox-catalyzed three-component oxidative radical-polar crossover strategy for constructing 1,2-alkylamination products. Cycloketone oxime derivatives were used as cyanoalkyl radical precursors and anilines were used as the nucleophiles. This facile protocol shows a good reaction yield and broad substrate scope.

The Journal of Organic ChemistryVol. 90(17)
Sichuan University (CN), West China Hospital of Sichuan University (CN)
Department of Science and Technology of Sichuan Province
Openalex Percentile: Top 16%
Catalytic C–H Functionalization Methods
1.87
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