Evidence map›Paper›PMID 42729712›Full record

ArticleACS omega2026

Fast Microwave-Assisted Ullmann-Type Coupling for the Synthesis of Multisubstituted Diaryl Ethers.

Dario Gentili, Gabriele Lupidi, Francesca Stella, Jo' Del Gobbo, Miriam Caviglia, Luca Barigelli, Maura Pellei, Carlo Santini, H V Rasika Dias, Enrico Marcantoni and 2 more

Abstract read
In one paragraph

Article in ACS omega, 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

12 authors.

Dario GentiliUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.
Gabriele LupidiUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.
Francesca StellaUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.
Jo' Del GobboUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.ORCID https://orcid.org/0009-0002-8969-0900
Miriam CavigliaUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.
Luca BarigelliUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.
Maura PelleiUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.ORCID https://orcid.org/0000-0001-5020-1730
Carlo SantiniUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.ORCID https://orcid.org/0000-0002-3942-1713
H V Rasika DiasDepartment of Chemistry and Biochemistry, The University of Texas at Arlington, Box 19065, Arlington, Texas 76019-0065, United States.ORCID https://orcid.org/0000-0002-2362-1331
Enrico MarcantoniUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.ORCID https://orcid.org/0000-0002-8686-3987
Cristina CimarelliUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.
Serena GabrielliUniversità degli Studi di Camerino, School of Science and Technology - Chemistry Division, Via Madonna delle Carceri, Camerino 62032, Italy.ORCID https://orcid.org/0000-0002-2048-5813

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A mild and rapid microwave-assisted Ullmann-type C-O coupling protocol catalyzed by copper-(II) complexes was developed and optimized for the efficient synthesis of a wide variety of diaryl ethers. The synthetic methodology is general and tolerant toward both electron-rich and electron-poor phenols and aryl halides. Furthermore, this protocol provides a practical and rapid methodology for preparing diaryl ethers with potential biological and pharmacological relevance and represents a rapid and operationally efficient alternative to conventional thermal methods, thereby widening the use of copper catalysis in organic synthesis.

Identifiers

PMID42729712
PMCPMC13563614

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.