Evidence map›Paper›PMID 41009514›Full record

ArticleInternational journal of molecular sciences2025

On the Question of the Regio-Orientation, Stereo-Orientation and Molecular Mechanism in the Cascade Cycloaddition/Rearrangement/Elimination Processes Leading to Nitro-Substituted Thiopyran Analogs: DFT Computational Study.

Mikołaj Sadowski, Ewa Dresler, Radomir Jasiński

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Mikołaj SadowskiCracow University of Technology, CUT Doctoral School, Faculty of Chemical Engineering and Technology, Warszawska 24, 31-155 Cracow, Poland.ORCID 0000-0002-1045-7093
Ewa DreslerŁukasiewicz Research Network-Institute of Heavy Organic Synthesis "Blachownia", Energetyków 9, 47-225 Kędzierzyn-Koźle, Poland.ORCID 0000-0001-5035-3056
Radomir JasińskiCracow University of Technology, Department of Organic Chemistry and Technology, Warszawska 24, 31-155 Cracow, Poland.ORCID 0000-0001-8555-6793

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sulfur-containing heterocyclic structures play an important role in modern biotechnology. Their synthesis is made possible by means of the hetero Diels-Alder reaction involving unsaturated sulfur compounds. In the framework of this paper, the molecular mechanism of the cycloaddition reactions between tioanalogs of the butadiene generated in situ with the participation of the

Indexed as

Cycloaddition ReactionCatalysisDensity Functional TheoryStereoisomerismcycloadditiondeaminationdensity functional theoryhetero Diels–Alder reactionLewis acid (LA) catalysisnitroalkenestepwise mechanism

Identifiers

PMID41009514
PMCPMC12469585

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.