Synthesis of Unsymmetrical 4,4′-Bipyridines through Base-Mediated Cross-Coupling between 4-Pyridyl Phosphonium Salts

Syntheses of unsymmetrical 4,4'-bipyridines were achieved through base-mediated cross-couplings of diverse 4-pyridyl phosphonium salts. This transition-metal- and oxidant-free protocol operates under mild conditions and tolerates a broad range of functional groups. Subsequent derivatization of the bipyridine products enabled the selective preparation of viologens and other valuable aromatic scaffolds. Mechanistic studies indicate the formation of an anionic pyridyl intermediate, which undergoes C-C bond formation through phosphorus ligand coupling or an S<sub>N</sub>Ar mechanism.

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Journal
Organic Letters
Published
2026-01-29
DOI
https://doi.org/10.1021/acs.orglett.5c05284
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Synthesis of Unsymmetrical 4,4′-Bipyridines through Base-Mediated Cross-Coupling between 4-Pyridyl Phosphonium Salts

Suman De Sarkar, Malekul Islam, Braja Kishor Paul, Fadil Faizal Mannighayil
Organic Letters
Catalytic C–H Functionalization Methods
article

Synthesis of Unsymmetrical 4,4′-Bipyridines through Base-Mediated Cross-Coupling between 4-Pyridyl Phosphonium Salts

Suman De Sarkar, Malekul Islam, Braja Kishor Paul, Fadil Faizal Mannighayil
article en

Abstract

Syntheses of unsymmetrical 4,4'-bipyridines were achieved through base-mediated cross-couplings of diverse 4-pyridyl phosphonium salts. This transition-metal- and oxidant-free protocol operates under mild conditions and tolerates a broad range of functional groups. Subsequent derivatization of the bipyridine products enabled the selective preparation of viologens and other valuable aromatic scaffolds. Mechanistic studies indicate the formation of an anionic pyridyl intermediate, which undergoes C-C bond formation through phosphorus ligand coupling or an S<sub>N</sub>Ar mechanism.

Organic LettersVol. 28(6)
Indian Institute of Science Education and Research Kolkata (IN)
Clean water and sanitation
Openalex Percentile: Top 72%
Catalytic C–H Functionalization Methods
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