Evidence map›Paper›PMID 42046454›Full record

ArticleChemSusChem2026

Merging Micellar Catalysis and C-H Activation: Silver-Free Direct Arylation of Fluoroarenes in Water.

Federico Belnome, Kristóf N Garami, Zoltán Varga, Judith Mihály, Pascal Hauk, Tamás Hergert, György M Keserű, Fabrice Gallou, Joanna Wencel-Delord, Péter Ábrányi-Balogh

Abstract read
In one paragraph

Article in ChemSusChem, 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

10 authors.

Federico BelnomeVan't Hoff Institute for Molecular Sciences (HIMS), University of Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0009-0009-8411-5211
Kristóf N GaramiMedicinal Chemistry Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Zoltán VargaBiological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Judith MihályBiological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Pascal HaukLaboratoire d'Innovation Moléculaire et Applications (UMR CNRS 7042), Université de Strasbourg, ECPM, Université de Haute Alsace, Strasbourg, France.
Tamás HergertThalesNano Inc., Budapest, Hungary.
György M KeserűMedicinal Chemistry Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Fabrice GallouChemical & Analytical Development, Novartis Pharma AG, Basel, Switzerland.ORCID https://orcid.org/0000-0001-8996-6079
Joanna Wencel-DelordInstitut für Organische Chemie, Am Hubland, Würzburg, Germany.ORCID https://orcid.org/0000-0002-7094-5443
Péter Ábrányi-BaloghMedicinal Chemistry Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID https://orcid.org/0000-0002-9284-5160

Funding

Doctoral Excellence Fellowship Programme DCEP-25-1-BME-53Horizon 2020 Framework Programme 860762János Bolyai Research Scholarship of the Hungarian Academy of SciencesNational Research Development and Innovation Fund of the Ministry of Culture and Innovation and the Budapest University of Technology and EconomicsNemzeti Kutatási Fejlesztési és Innovációs Hivatal 2020-1.1.2-PIACI-KFI-2020-00021Nemzeti Kutatási Fejlesztési és Innovációs Hivatal ADVANCED 150077Nemzeti Kutatási Fejlesztési és Innovációs Hivatal RGH 151414Nemzeti Kutatási Fejlesztési és Innovációs Hivatal RRF-2.3.1-21-2022-00015Nemzeti Kutatási Fejlesztési és Innovációs Hivatal TKP2021-EGA-31
6 · The paper itself

Abstract

The direct arylation of fluoroarenes is a powerful but sustainability-limited transformation, as most established protocols rely on organic solvents and stoichiometric silver additives. Here, we report the first silver-free palladium-catalyzed C-H arylation of fluoroarenes in water containing self-assembled surfactant structures (micelles) as reaction medium. Using the designer surfactant PS-750-M, this sustainable method enables the coupling of diverse pyridines and fluoroarenes under mild conditions, displaying broad functional-group tolerance while fully eliminating organic co-solvents. Mechanistic studies, including kinetics, FT-IR spectroscopy, dynamic light scattering (DLS), and freeze-fracture combined transmission electron microscopy (FF-TEM), reveal the nature of interactions between the catalyst, substrates and distinct micellar domains, providing insight into microenvironmental effects on reactivity and selectivity. The robustness of the catalytic system further allows tandem one-pot sequences, such as C-H arylation/S

Identifiers

PMID42046454
PMCPMC13122133

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Registered trials

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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.