Evidence map›Paper›PMID 35423136›Full record

ArticleRSC advances2021

Synthesis, crystal structure and antibacterial studies of dihydropyrimidines and their regioselectively oxidized products.

Alakbar E Huseynzada, Christian Jelch, Haji Vahid N Akhundzada, Sarra Soudani, Cherif Ben Nasr, Aygun Israyilova, Filippo Doria, Ulviyya A Hasanova, Rana F Khankishiyeva, Mauro Freccero

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in RSC advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
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, 21 citations in OpenAlex.

  1. Cu(OTf)Beilstein journal of organic chemistry · 2025
    Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 4 countries.

Alakbar E HuseynzadaBaku State University, ICRL Z. Khalilov 23 Baku AZ 1148 Azerbaijan alakbar.huseynzada1117@gmail.com.ORCID 0000-0002-6342-4260
Christian JelchUniversité de Lorraine, CNRS, CRM2 54000 Nancy France.ORCID 0000-0002-2655-0313
Haji Vahid N AkhundzadaBaku State University, ICRL Z. Khalilov 23 Baku AZ 1148 Azerbaijan alakbar.huseynzada1117@gmail.com.
Sarra SoudaniLaboratoire de Chimie des Matériaux, Faculté des Sciences de Bizerte, Université de Carthage 7021 Zarzouna Tunisia.
Cherif Ben NasrLaboratoire de Chimie des Matériaux, Faculté des Sciences de Bizerte, Université de Carthage 7021 Zarzouna Tunisia.
Aygun IsrayilovaDepartment of Molecular biology and Biotechnology, Baku State University Z. Khalilov 23 Baku AZ 1148 Azerbaijan.
Filippo DoriaUniversita di Pavia V.le Taramelli 10 27100 Pavia Italy.
Ulviyya A HasanovaBaku State University, ICRL Z. Khalilov 23 Baku AZ 1148 Azerbaijan alakbar.huseynzada1117@gmail.com.
Rana F KhankishiyevaInstitute of Radiation Problems of ANAS B. Vahabzada 9 Baku AZ 1143 Azerbaijan.ORCID 0000-0002-4532-9913
Mauro FrecceroUniversita di Pavia V.le Taramelli 10 27100 Pavia Italy.
Baku State University · AZAzerbaijan National Academy of Sciences · AZÉcole Supérieure des Sciences de l'Ingénierie Commerciale · MAUniversity of Pavia · ITLaboratoire de Cristallographie, Résonance Magnétique et Modélisations · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The syntheses and investigations of new biologically active derivatives of dihydropyrimidines by Biginelli reaction in the presence of copper triflate are reported. Due to the fact that salicylaldehyde and its derivatives under Biginelli reaction conditions can lead to the formation of 2 types of dihydropyrimidines, the influence of copper triflate on product formation was also investigated. In addition to this, regioselective oxidation of dihydropyrimidines was performed in the presence of cerium ammonium nitrate and novel oxidized dihydropyrimidines were obtained. Single crystals of some of them were obtained and as a result, the structures of them were investigated by X-ray diffraction method, which allows determining the presence of hydrogen bonds in their structures. In addition to this, the presence of hydrogen bonds in their structures affects the formation of the corresponding tautomer during oxidizing of dihydropyrimidines. Since dihydropyrimidines are claimed to be biologically active compounds, activities of the synthesized compounds were studied against

Identifiers

PMID35423136
PMCPMC8694924
OpenAlexW4211178466

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.