Evidence map›Paper›PMID 41014277›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026

Versatile Palladium-Catalyzed C-H Arylation of Fluoroarenes with 2-Chloropyridine Derivatives.

Federico Belnome, Péter P Fehér, András Stirling, Csongor G Németh, Tamás Hergert, György M Keserű, Péter Ábrányi-Balogh

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Federico BelnomeVan 't Hoff Institute for Molecular Sciences (HIMS), University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands.
Péter P FehérTheoretical Chemistry Research Group, HUN-REN Research Centre for Natural Sciences of the Hungarian Academy of Sciences, Magyar tudósok körútja 2. 1117, Budapest, Hungary.ORCID https://orcid.org/0000-0002-6927-4523
András StirlingTheoretical Chemistry Research Group, HUN-REN Research Centre for Natural Sciences of the Hungarian Academy of Sciences, Magyar tudósok körútja 2. 1117, Budapest, Hungary.
Csongor G NémethMedicinal Chemistry Research Group, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2. 1117, Budapest, Hungary.
Tamás HergertThalesNano Inc., Záhony street 7, Budapest, H-1031, Hungary.
György M KeserűMedicinal Chemistry Research Group, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2. 1117, Budapest, Hungary.
Péter Ábrányi-BaloghMedicinal Chemistry Research Group, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2. 1117, Budapest, Hungary.ORCID https://orcid.org/0000-0002-9284-5160

Funding

H2020 European Research Council 860762Nemzeti Kutatási Fejlesztési és Innovációs Hivatal PharmaLab (RRF-2.3.1-21-2022-00015)
6 · The paper itself

Abstract

Direct C─H arylation of fluoroarenes with 2-halopyridines remains underexplored, due to the low reactivity of both partners and the reliance on harsh conditions or toxic solvents. Herein, we report a general and sustainable method for the C─H arylation of fluoroarenes with 2-chloropyridines using Pd/SPhos as a simple catalytic system in isopropyl acetate. The protocol employs inexpensive starting materials, shows broad functional group tolerance, and delivers a wide range of 2-(fluorinated aryl)pyridines in up to 90% yield. Substrate scope studies uncovered key substituent effects on both coupling partners, while Density Functional Theory (DFT)-supported mechanistic analysis rationalized the observed reactivity and chemoselectivity. This research advances sustainable and practical methodologies for the synthesis of complex fluorinated aromatic compounds with potential applications in materials science, agrochemistry, and medicinal chemistry.

Indexed as

C‐H arylationcross‐couplingDFTfluorinated arenesmechanismpyridinesustainability

Identifiers

PMID41014277
PMCPMC13411621

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.