Evidence map›Paper›PMID 42312144›Full record

ArticleChemical science2026

Switchable reactivity of homopropargylic alcohols towards γ-arylated ketones and α-arylated tetrahydrofurans in HFIP.

Claire Miesch, Ewelina Krolicka, Robert J Mayer, David Lebœuf

Abstract read
In one paragraph

Article in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Claire MieschLaboratoire d'Innovation Moléculaire et Applications (LIMA), CNRS, UMR 7042, Université de Strasbourg, Université de Haute-Alsace 25 rue Becquerel 67000 Strasbourg France dleboeuf@unistra.fr.ORCID https://orcid.org/0009-0004-4912-8299
Ewelina KrolickaLaboratoire d'Innovation Moléculaire et Applications (LIMA), CNRS, UMR 7042, Université de Strasbourg, Université de Haute-Alsace 25 rue Becquerel 67000 Strasbourg France dleboeuf@unistra.fr.ORCID https://orcid.org/0009-0007-6168-6244
Robert J MayerTechnical University of Munich, School of Natural Sciences, Department Chemie 85748 Garching Germany robert.j.mayer@tum.de.ORCID https://orcid.org/0000-0002-9864-7042
David LebœufLaboratoire d'Innovation Moléculaire et Applications (LIMA), CNRS, UMR 7042, Université de Strasbourg, Université de Haute-Alsace 25 rue Becquerel 67000 Strasbourg France dleboeuf@unistra.fr.ORCID https://orcid.org/0000-0001-5720-7609

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A divergent synthetic strategy to access γ-arylated ketones and α-arylated tetrahydrofurans from readily available homopropargylic alcohols and arene nucleophiles is reported. This method expands the accessible chemical space of γ-arylated ketones

Identifiers

PMID42312144
PMCPMC13270797

What OpenQuestion holds

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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.