Synergistic Photocatalysis of Acridinium Salts and Pyridine <i>N</i> -Oxides for α-Aminoalkylation with <i>N</i> -Methylsulfonamides

This study presents a synergistic photocatalytic method using acridinium salts and pyridine <i>N</i>-oxides for the Giese reaction between <i>N</i>-methylsulfonamides and olefins, which utilizes <i>N</i>-methylsulfonamides as α-aminoalkylating reagents. Notable features of this approach include mild reaction conditions, excellent atom economy, good site selectivity, a broad substrate scope, and the ability to enable postmodification of complex drug fragments.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-11-11
DOI
https://doi.org/10.1021/acs.joc.5c01813
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81
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article

Synergistic Photocatalysis of Acridinium Salts and Pyridine N -Oxides for α-Aminoalkylation with N -Methylsulfonamides

Lipeng Qiao, Kai Sun, Bing Yu, Zi Yang et al.
3 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
2.81
article

Synergistic Photocatalysis of Acridinium Salts and Pyridine N -Oxides for α-Aminoalkylation with N -Methylsulfonamides

Lipeng Qiao, Kai Sun, Bing Yu, Zi Yang, Xi Chen, Xiaolan Chen, Zhichao Zhang, Lingbo Qu, Wumeng Yang
article en
3 citations

Abstract

This study presents a synergistic photocatalytic method using acridinium salts and pyridine <i>N</i>-oxides for the Giese reaction between <i>N</i>-methylsulfonamides and olefins, which utilizes <i>N</i>-methylsulfonamides as α-aminoalkylating reagents. Notable features of this approach include mild reaction conditions, excellent atom economy, good site selectivity, a broad substrate scope, and the ability to enable postmodification of complex drug fragments.

The Journal of Organic ChemistryVol. 90(46)
Changsha Medical University (CN), Nanjing Forestry University (CN), Hunan Normal University (CN), Zhengzhou University (CN), Henan Academy of Sciences (CN)
Openalex Percentile: Top 9%
Catalytic C–H Functionalization Methods
2.81
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