Evidence map›Paper›PMID 42357478›Full record

ReviewMolecules (Basel, Switzerland)2026

Recent Advances in Quinoline Synthesis: Sustainable Catalytic Strategies and Emerging Methodologies.

Ignacio M López-Coca, Shima Ghafouriraz, Silvia Izquierdo, Carlos J Durán-Valle, Mohammad Qandalee, Alireza Soltani

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Ignacio M López-CocaDepartment of Organic and Inorganic Chemistry, School of Technology, Universidad de Extremadura, 10003 Cáceres, Spain.ORCID 0000-0001-9120-4495
Shima GhafourirazDepartment of Organic and Inorganic Chemistry, School of Technology, Universidad de Extremadura, 10003 Cáceres, Spain.
Silvia IzquierdoDepartment of Organic and Inorganic Chemistry, School of Technology, Universidad de Extremadura, 10003 Cáceres, Spain.ORCID 0009-0000-3087-4698
Carlos J Durán-ValleDepartment of Organic and Inorganic Chemistry, Faculty of Sciences, Universidad de Extremadura, 06006 Badajoz, Spain.ORCID 0000-0002-2507-4650
Mohammad QandaleeDepartment of Basic Sciences, Ga.C., Islamic Azad University, Garmsar 3581631167, Iran.ORCID 0000-0002-3404-8577
Alireza SoltaniGolestan Rheumatology Research Center, Biomedical Research Institute, Golestan University of Medical Sciences, Gorgan 4934174515, Iran.ORCID 0000-0002-4739-636X

Funding

European Regional Development Fund IB24227Government of Extremadura IB24227
6 · The paper itself

Abstract

Quinoline derivatives constitute a privileged class of nitrogen-containing heterocycles with extensive applications in medicinal chemistry, agrochemicals, materials science, and functional organic materials. Owing to their broad biological and industrial relevance, the development of efficient, selective, and sustainable synthetic methodologies for quinoline construction remains an active area of research. This review provides a comprehensive overview of recent advances in quinoline synthesis, with particular emphasis on catalytic strategies aligned with the principles of green and sustainable chemistry. Classical transformations, including the Friedländer, Skraup, and Povarov reactions, are revisited in the context of modern catalytic developments that improve reaction efficiency, substrate scope, selectivity, and environmental compatibility. Special attention is devoted to homogeneous and heterogeneous catalytic systems based on both platinum-group and earth-abundant transition metals, highlighting the growing importance of borrowing-hydrogen and acceptorless dehydrogenative coupling methodologies. Recent progress in nanocatalysis, photocatalysis, multicomponent reactions, ionic-liquid-mediated transformations, and metal-free protocols is also critically discussed. Furthermore, solvent-free processes, microwave-assisted synthesis, and recyclable catalytic systems are examined as practical approaches toward minimizing waste generation and energy consumption. Mechanistic aspects, catalytic design principles, substrate limitations, and sustainability metrics are evaluated throughout the review to provide a critical perspective on current methodologies. Collectively, the advances summarized herein demonstrate the rapid evolution of quinoline synthesis toward more atom-economical, environmentally benign, and operationally efficient processes, while also identifying future opportunities for the development of next-generation catalytic platforms for quinoline-based heterocycle construction.

Indexed as

Friedländer reactiongreen chemistryheterocyclic compoundsheterogeneous catalysisPovarov reactionquinoline synthesis

Identifiers

PMID42357478
PMCPMC13304786

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Registered trials

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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.