Evidence map›Paper›PMID 40980844›Full record

ArticleChemSusChem2025

A Radical-Based, Transition Metal-Free Approach for Diaryl Ketone Synthesis.

Dongjie Wang, Jordan Garo, Yinpeng Wang, Jean-Marc Sotiropoulos, Marc Taillefer

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ChemSusChem, 2025. 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

5 authors.

Dongjie WangDépartement Chimie & Matériaux Moléculaire, Institut Charles Gerhardt de Montpellier, CNRS, ENSCM, University of Montpellier, 1919, route de Mende, 34293, Montpellier Cedex 5, France.
Jordan GaroE2S UPPA, CNRS, IPREM, Université de Pau et des Pays de l'Adour, Technopôle Hélioparc, 2 avenue du Président Pierre Angot, 64053, Pau Cedex 9, France.
Yinpeng WangDépartement Chimie & Matériaux Moléculaire, Institut Charles Gerhardt de Montpellier, CNRS, ENSCM, University of Montpellier, 1919, route de Mende, 34293, Montpellier Cedex 5, France.
Jean-Marc SotiropoulosE2S UPPA, CNRS, IPREM, Université de Pau et des Pays de l'Adour, Technopôle Hélioparc, 2 avenue du Président Pierre Angot, 64053, Pau Cedex 9, France.ORCID https://orcid.org/0000-0001-9513-3639
Marc TailleferDépartement Chimie & Matériaux Moléculaire, Institut Charles Gerhardt de Montpellier, CNRS, ENSCM, University of Montpellier, 1919, route de Mende, 34293, Montpellier Cedex 5, France.ORCID https://orcid.org/0000-0003-2991-5418

Funding

Académie des SciencesChina Scholarship CouncilCNRSDirection du Numérique of the Université de Pau et Pays de l'Adour
6 · The paper itself

Abstract

Diaryl ketones represent a pivotal class of compounds, widely used in pharmaceuticals, agrochemicals, and materials science. Driven by the urgent need for safer and more sustainable synthetic methodologies, developing innovative approaches in this area has become a critical priority for both academia and industry. In this context, a straightforward yet novel one-pot strategy for synthesizing a broad array of diaryl ketones, including valuable target molecules, is presented. This approach diverges from conventional methods by employing a radical process, in which aryl halides react with benzonitriles in a basic medium, relying exclusively on the organic reductant pair KO

Indexed as

DFT calculationsdiaryl ketonesradical mechanismssustainable chemistrytransition metal‐free processes

Identifiers

PMID40980844
PMCPMC12584960

What OpenQuestion holds

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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.