Evidence map›Paper›PMID 39069813›Full record

ReviewCurrent topics in medicinal chemistry2025

Green Synthesis of Bioactive Pyrrole Derivatives

Berrichi Amina, Bachir Redouane

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current topics in medicinal 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

2 authors.

Berrichi AminaLaboratory of Catalysis and Synthesis in Organic Chemistry, University of Tlemcen, BP 119, 13000, Tlemcen, Algeria.ORCID 0000-0003-2586-6428
Bachir RedouaneLaboratory of Catalysis and Synthesis in Organic Chemistry, University of Tlemcen, BP 119, 13000, Tlemcen, Algeria.ORCID 0000-0001-6260-2179

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pyrrole derivatives are known as building blocks for the synthesis of biological compounds and pharmaceutical drugs. Several processes were employed to synthesize pyrroles, including Hantzsch, Paal-Knorr, and cycloaddition of dicarbonyl compounds reaction. Using catalysts like nanoparticles, metal salts, and heterogeneous ones was necessary to obtain the targeted pyrrole structure. Also, to afford more active pyrrole compounds, heterocyclic molecules such as imidazole or other rings were used in the synthesis as amines. This review presents heterogeneous catalysts since 2010 for the green synthesis of bioactive pyrroles in a one-pot multi-component reaction. Additionally, each synthetic method included a demonstration of the suggested mechanisms. Diakylacetylenedicarboxylate, dicarbonyl group, amines, furans, and acetylene group are consolidated to yield biological pyrroles through the heterogeneous catalysts. Finally, various pyrrole-performed activities were displayed, such as antibacterial, anti-inflammatory, analgesic, and other significant activities.

Indexed as

Anti-Bacterial AgentsAnti-Inflammatory Agents, Non-SteroidalGreen Chemistry TechnologyPyrrolesAnti-Inflammatory AgentsCatalysisHumansMolecular StructureAnti-Bacterial AgentsAnti-Inflammatory AgentsAnti-Inflammatory Agents, Non-SteroidalPyrrolesAcetylene group.Bioactive pyrrolesDicarbonyl groupHeterogeneous catalystsNanoparticlesPyrrole derivatives

Identifiers

What OpenQuestion holds

Textmetadata
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.