Evidence map›Paper›PMID 37746335›Full record

ArticleRSC advances2023

BiCl

Yousra Ouafa Bouone, Abdeslem Bouzina, Rayene Sayad, Abdelhak Djemel, Farouk Benaceur, Abdelhalim Zoukel, Malika Ibrahim-Ouali, Nour-Eddine Aouf, Fouzia Bouchareb

Abstract read
In one paragraph

Article in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

9 authors.

Yousra Ouafa BouoneLaboratory of Applied Organic Chemistry, Bioorganic Chemistry Group, Department of Chemistry, Sciences Faculty, Badji-Mokhtar - Annaba University Box 12 23000 Annaba Algeria abdeslem.bouzina@univ-annaba.dz bouzinaabdeslem@yahoo.fr.ORCID https://orcid.org/0000-0002-8908-8912
Abdeslem BouzinaLaboratory of Applied Organic Chemistry, Bioorganic Chemistry Group, Department of Chemistry, Sciences Faculty, Badji-Mokhtar - Annaba University Box 12 23000 Annaba Algeria abdeslem.bouzina@univ-annaba.dz bouzinaabdeslem@yahoo.fr.
Rayene SayadLaboratory of Applied Organic Chemistry, Bioorganic Chemistry Group, Department of Chemistry, Sciences Faculty, Badji-Mokhtar - Annaba University Box 12 23000 Annaba Algeria abdeslem.bouzina@univ-annaba.dz bouzinaabdeslem@yahoo.fr.
Abdelhak DjemelResearch Unit in Medicinal Plants, URPM, Research Center of Biotechnology, CRBt 3000 Laghouat 25000 Constantine Algeria.
Farouk BenaceurResearch Unit in Medicinal Plants, URPM, Research Center of Biotechnology, CRBt 3000 Laghouat 25000 Constantine Algeria.
Abdelhalim ZoukelTechnical Platform of Physico-Chemical Analysis (PTAPC-Laghout-CRAPC), University of Laghouat Laghouat 03000 Algeria.
Malika Ibrahim-OualiAix Marseille Univ, CNRS, Centrale Marseille, iSm2 F-13397 Marseille France.ORCID https://orcid.org/0000-0001-7272-9392
Nour-Eddine AoufLaboratory of Applied Organic Chemistry, Bioorganic Chemistry Group, Department of Chemistry, Sciences Faculty, Badji-Mokhtar - Annaba University Box 12 23000 Annaba Algeria abdeslem.bouzina@univ-annaba.dz bouzinaabdeslem@yahoo.fr.
Fouzia BoucharebLaboratory of Applied Organic Chemistry, Synthesis of Biomolecules and Molecular Modelling Group, Department of Chemistry, Sciences Faculty, Badji-Mokhtar - Annaba University Box 12 23000 Annaba Algeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traditional chemical synthesis, which involves the use of dangerous protocols, hazardous solvents, and toxic products and catalysts, is considered environmentally inappropriate and harmful to human health. Bearing in mind its numerous drawbacks, it has become crucial to substitute conventional chemistry with green chemistry which is safer, more ecofriendly and more effective in terms of time and selectivity. Elaborating synthetic protocols producing interesting new compounds using both microwave heating and heterogeneous non-toxic catalysts is acknowledged as a green approach that avoids many classical chemistry-related problems. In the current study, β-enaminones were used as precursors to the synthesis of modified 4-hydroxy-2-quinolone analogues. The synthesis was monitored in a benign way under microwave irradiation and was catalyzed by bismuth chloride III in an amount of 20 mol%. This method is privileged by using a non-corrosive, non-toxic, low-cost and available bismuth Lewis acid catalyst that has made it more respectful to the demands of green chemistry. The synthesized compounds were obtained in moderate to good yields (51-71%) and were characterized by

Identifiers

PMID37746335
PMCPMC10517106

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.