Palladium‐Catalyzed Heck‐Type Double Arylation of 1,2‐Dihydropyridines

ABSTRACT We report a site‐ and regioselective Heck‐type double arylation of substituted 1,2‐dihydropyridines. This transformation provides access to 2‐substituted 3,6‐diarylated 1,2‐dihydropyridines from readily available dearomatized pyridine derivatives. Two complementary strategies were developed: a direct double arylation approach that rapidly furnishes symmetrically diarylated products and a sequential arylation strategy that enables the controlled introduction of two different aryl groups. Both approaches proceed with generally high selectivity and tolerate different 1,2‐dihydropyridine substrates and aryl iodides. Overall, this study provides a concise entry to highly substituted 1,2‐dihydropyridine scaffolds.

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Publication Details

Journal
Helvetica Chimica Acta
Published
2026-10-31
DOI
https://doi.org/10.1002/hlca.70108
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

Palladium‐Catalyzed Heck‐Type Double Arylation of 1,2‐Dihydropyridines

Zackaria Nairoukh, Haining Li
Helvetica Chimica Acta
Catalytic Cross-Coupling Reactions
article

Palladium‐Catalyzed Heck‐Type Double Arylation of 1,2‐Dihydropyridines

Zackaria Nairoukh, Haining Li
article en

Abstract

ABSTRACT We report a site‐ and regioselective Heck‐type double arylation of substituted 1,2‐dihydropyridines. This transformation provides access to 2‐substituted 3,6‐diarylated 1,2‐dihydropyridines from readily available dearomatized pyridine derivatives. Two complementary strategies were developed: a direct double arylation approach that rapidly furnishes symmetrically diarylated products and a sequential arylation strategy that enables the controlled introduction of two different aryl groups. Both approaches proceed with generally high selectivity and tolerate different 1,2‐dihydropyridine substrates and aryl iodides. Overall, this study provides a concise entry to highly substituted 1,2‐dihydropyridine scaffolds.

Helvetica Chimica Acta
Hebrew University of Jerusalem (IL)
Openalex Percentile: Top 26%
Catalytic Cross-Coupling Reactions
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