Evidence map›Paper›PMID 41055363›Full record

ReviewChemical record (New York, N.Y.)2025

Recent Synthetic Advances in C-H/N-H Functionalization of 1H-Pyrazoles: Diverse Strategies Across Variously Substituted Scaffolds.

Karolina Dzedulionytė Müldür, Asta Žukauskaitė, Algirdas Šačkus, Eglė Arbačiauskienė

Abstract readReview
In one paragraph

Review in Chemical record (New York, N.Y.), 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

4 authors.

Karolina Dzedulionytė MüldürDepartment of Organic Chemistry, Faculty of Chemical Technology, Kaunas University of Technology, Radvilėnų pl. 19, LT-50254, Kaunas, Lithuania.ORCID https://orcid.org/0000-0001-7533-1988
Asta ŽukauskaitėDepartment of Chemical Biology, Faculty of Science, Palacký University Olomouc, Šlechtitelů 27, CZ-77900, Olomouc, Czech Republic.ORCID https://orcid.org/0000-0001-6759-8789
Algirdas ŠačkusDepartment of Organic Chemistry, Faculty of Chemical Technology, Kaunas University of Technology, Radvilėnų pl. 19, LT-50254, Kaunas, Lithuania.ORCID https://orcid.org/0000-0002-1514-4934
Eglė ArbačiauskienėDepartment of Organic Chemistry, Faculty of Chemical Technology, Kaunas University of Technology, Radvilėnų pl. 19, LT-50254, Kaunas, Lithuania.ORCID https://orcid.org/0000-0003-1365-9990

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review briefly and systematically overviews C-H and N-H functionalization reactions of pyrazoles, aimed at creating new CC and Cheteroatom bonds on the pyrazole ring. It discusses various strategies, including traditional cross-coupling reactions that necessitate prefunctionalized pyrazoles as well as direct functionalization reactions, which offer a more efficient approach to obtaining a diverse array of functionalized derivatives in only one step.

Indexed as

catalysispyrazoleregioselectivityselective functionalization

Identifiers

PMID41055363
PMCPMC12706575

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.