Radical C4−H Arylation of 1,4‐Dihydropyridines with Cyanoarenes

Abstract 4‐Aryl‐1,4‐dihydropyridines are prevalent pharmacophores and versatile building blocks in medicinal and synthetic chemistry. Herein, we demonstrated a mechanistically distinct radical‐radical cross‐coupling approach to 4‐aryl‐1,4‐dihydropyridines, via direct C4−H arylation of 1,4‐dihydropyridines with readily available cyanoarenes. This mild protocol is initiated by the direct photoexcitation of 1,4‐dihydropyridines, eliminating the need for expensive photocatalysts and enabling operation under ambient air conditions.

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Publication Details

Journal
Helvetica Chimica Acta
Published
2024-11-21
DOI
https://doi.org/10.1002/hlca.202400162
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.25
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article

Radical C4−H Arylation of 1,4‐Dihydropyridines with Cyanoarenes

Shiqin Qiu, Peng Xu, Huaixuan Guo
1 citations
Helvetica Chimica Acta
Radical Photochemical Reactions
0.25
article

Radical C4−H Arylation of 1,4‐Dihydropyridines with Cyanoarenes

Shiqin Qiu, Peng Xu, Huaixuan Guo
article en
1 citations

Abstract

Abstract 4‐Aryl‐1,4‐dihydropyridines are prevalent pharmacophores and versatile building blocks in medicinal and synthetic chemistry. Herein, we demonstrated a mechanistically distinct radical‐radical cross‐coupling approach to 4‐aryl‐1,4‐dihydropyridines, via direct C4−H arylation of 1,4‐dihydropyridines with readily available cyanoarenes. This mild protocol is initiated by the direct photoexcitation of 1,4‐dihydropyridines, eliminating the need for expensive photocatalysts and enabling operation under ambient air conditions.

Helvetica Chimica ActaVol. 107(12)
Shanghai University (CN)
Clean water and sanitation
Openalex Percentile: Top 46%
Radical Photochemical Reactions
0.25
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