Evidence map›Paper›PMID 41183380›Full record

ArticleChemphyschem : a European journal of chemical physics and physical chemistry2025

C-N Coupling of 3-Aminothiophene with Substituted Benzenediazonium Cations: Carbon Nucleophilicity, Hyper-Ortho Effects, and Predictive Modeling of Structural Analogs.

R El Abed, T Slama, F Mahdhaoui, T Boubaker

Abstract read
In one paragraph

Article in Chemphyschem : a European journal of chemical physics and physical chemistry, 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. 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

4 authors.

R El AbedLaboratoire de Chimie Hétérocyclique, Produits Naturels et Réactivité (LR11SE39), Faculté des Sciences de Monastir, Université de Monastir, Avenue de l'Environnement, 5019, Monastir, Tunisie.
T SlamaLaboratoire de Chimie Hétérocyclique, Produits Naturels et Réactivité (LR11SE39), Faculté des Sciences de Monastir, Université de Monastir, Avenue de l'Environnement, 5019, Monastir, Tunisie.
F MahdhaouiLaboratoire de Chimie Hétérocyclique, Produits Naturels et Réactivité (LR11SE39), Faculté des Sciences de Monastir, Université de Monastir, Avenue de l'Environnement, 5019, Monastir, Tunisie.
T BoubakerLaboratoire de Chimie Hétérocyclique, Produits Naturels et Réactivité (LR11SE39), Faculté des Sciences de Monastir, Université de Monastir, Avenue de l'Environnement, 5019, Monastir, Tunisie.ORCID https://orcid.org/0000-0003-3670-7828

Funding

Ministry of Higher Education and Scientific Research
6 · The paper itself

Abstract

This review has kinetically investigated the electrophilic attack of 3-aminothiophene 1 by a series of para-substituted benzenediazonium cations 7a-7h in 50% H

Indexed as

3‐aminothiophenekineticsMayr–Patz reactivity scalenucleophilicitystructure–reactivity relationshipssubstituent electronic effects

Identifiers

PMID41183380
PMCPMC12710183

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.