Evidence map›Paper›PMID 41752522›Full record

ArticleMolecules (Basel, Switzerland)2026

Multicomponent Reaction for the Synthesis of β-Ketosulfides in Deep Eutectic Solvents.

Chiara Falcini, David Jaén-Herrera, Rosario Fernández, Andrés R Alcántara, Gonzalo de Gonzalo

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 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

5 authors.

Chiara FalciniOrganic Chemistry Department, University of Sevilla, c/Prof. García González, 1, 41012 Sevilla, Spain.ORCID 0009-0009-5163-2079
David Jaén-HerreraOrganic Chemistry Department, University of Sevilla, c/Prof. García González, 1, 41012 Sevilla, Spain.
Rosario FernándezOrganic Chemistry Department, University of Sevilla, c/Prof. García González, 1, 41012 Sevilla, Spain.ORCID 0000-0002-1755-1525
Andrés R AlcántaraDepartment of Chemistry in Pharmaceutical Sciences, Faculty of Pharmacy, Complutense University of Madrid, Plaza de Ramón y Cajal s/n, 28040 Madrid, Spain.
Gonzalo de GonzaloOrganic Chemistry Department, University of Sevilla, c/Prof. García González, 1, 41012 Sevilla, Spain.ORCID 0000-0002-0863-680X

Funding

Horizon Europe 101072731
6 · The paper itself

Abstract

The use of Type III Deep Eutectic Solvents (DESs) as both solvents and cocatalysts enable the one-pot synthesis of several β-ketosulfides, structural motifs commonly found in biologically active compounds, via a multicomponent reaction (MCR) involving 2-bromoketones, alkyl or benzyl halides, and potassium thioacetate in basic medium. Under these conditions, it was possible to avoid not only the use of the non-eco-friendly solvent dimethylformamide (DMF), but also an additional hydrolytic step previously reported for the preparation of these molecules. The MCR conducted in the presence of the DES ChCl:Gly (1:2) was optimized through the evaluation of different reaction parameters. Notably, the non-conventional medium could be recycled up to four times without any appreciable loss of catalytic activity. Environmental metrics, including the E factor, E+ factor, and Global Warming Potential (GWP), were calculated for the process both in the presence and absence of the DES, demonstrating improved environmental performance when the DES was employed.

Indexed as

deep eutectic solventsE-factorglobal warming potentialgreen chemistrymulticomponent reactionsβ-ketosulfides

Identifiers

PMID41752522
PMCPMC12943558

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.