Evidence map›Paper›PMID 40270886›Full record

ArticleACS catalysis2025

Microfluidic Photocatalytic Ring Expansion of Sulfonium Salts for the Synthesis of Cyclic Sulfides.

Jorge Humbrías-Martín, José J Garrido-González, Katy Medrano-Uribe, Giorgio Pelosi, Loris Laze, Luca Dell'Amico

Abstract read
In one paragraph

Article in ACS catalysis, 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. Review
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

6 authors.

Jorge Humbrías-MartínDepartment of Chemical Sciences, University of Padova, Via Francesco Marzolo 1, 35131 Padova, Italy.
José J Garrido-GonzálezDepartment of Chemical Sciences, University of Padova, Via Francesco Marzolo 1, 35131 Padova, Italy.ORCID https://orcid.org/0000-0001-7696-7902
Katy Medrano-UribeDepartment of Chemical Sciences, University of Padova, Via Francesco Marzolo 1, 35131 Padova, Italy.
Giorgio PelosiDepartment of Chemistry, Life Sciences and Environmental Sustain-ability, University of Parma, Parco Area Delle Science 17, 43124 Parma, Italy.ORCID https://orcid.org/0000-0002-7946-0602
Loris LazeInstituto de Síntesis Orgánica (ISO) and Departamento de Química Orgánica, Universidad de Alicante, 03080 Alicante, Spain.
Luca Dell'AmicoDepartment of Chemical Sciences, University of Padova, Via Francesco Marzolo 1, 35131 Padova, Italy.ORCID https://orcid.org/0000-0003-0423-9628

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclic sulfides are relevant building blocks in medicinal and synthetic chemistry, with applications ranging from drug discovery to materials science. However, the synthesis of medium-sized cyclic sulfides (6-8-membered rings) remains largely underdeveloped. Herein, we report a photocatalytic ring-expansion strategy for sulfonium salts, granting access to six-, seven-, and eight-membered cyclic sulfides with very high regio- and diastereocontrol. The implementation of the method under continuous flow was key to increasing the efficiency and minimizing product decomposition. Mechanistic investigations revealed the formation of benzylic radicals and carbocation intermediates that control the high regio- and diastereoselectivity observed. Finally, the synthetic utility of this approach was demonstrated in the synthesis of cyclic sulfoxides and sulfones, which can be easily obtained from the corresponding sulfide products.

Identifiers

PMID40270886
PMCPMC12012829

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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.