Evidence map›Paper›PMID 42860501›Full record

ReviewTopics in current chemistry (Cham)2026

Recent Advances in the Gewald Reaction: A Valuable Tool for the Synthesis of Thiophene Derivatives.

Lubna Khan, Maryam Abbasi, Mohd Kamil Hussain, Rashid Ali

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In one paragraph

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

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0citing papers in PubMed
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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

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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

4 authors.

Lubna Khan *Organic and Supramolecular Functional Materials Research Laboratory, Department of Chemistry, Jamia Millia Islamia, Jamia Nagar, Okhla, New Delhi, 110025, India.
Maryam Abbasi *Organic and Supramolecular Functional Materials Research Laboratory, Department of Chemistry, Jamia Millia Islamia, Jamia Nagar, Okhla, New Delhi, 110025, India.
Mohd Kamil HussainDepartment of Chemistry, Govt. Raza P.G. College, 244901, Rampur, UP, India.
Rashid AliOrganic and Supramolecular Functional Materials Research Laboratory, Department of Chemistry, Jamia Millia Islamia, Jamia Nagar, Okhla, New Delhi, 110025, India. rali1@jmi.ac.in.

Funding

Science and Engineering Research Board ECR/2017/000821
6 · The paper itself

Abstract

Since its first report in 1961, the Gewald reaction has evolved as a powerful tool for the construction of the 2-aminothiophene framework. Toward the synthesis of 2-aminothiophenes, in the past 4-5 decades, a plethora of publications have appeared in the scientific literature, but Gewald's strategy remains dominant among other methods due to its simplicity and the development of its different versions. This review showcases recent advances in Gewald methodologies for the fabrication of thiophene derivatives over the past one and a half decades, since the last update was reviewed. The present comprehensive manuscript, besides covering the traditional Gewald procedures, also exposes modern developments-for example, microwave and ultrasound-assisted synthesis, and the use of ionic liquids (ILs), deep eutectic solvents (DESs), and phase-transfer catalysts (PTCs). Herein, we have not only illustrated the details of the advancements in this still-emerging field, but have also illustrated its superiority, simplicity, and advantages in comparison with the existing methods.

Indexed as

ThiophenesCatalysisDeep Eutectic SolventsIonic LiquidsMicrowavesMolecular StructureDeep Eutectic SolventsIonic LiquidsThiophenes2-aminothiophenesGewald reactionHeterocyclesNamed reaction and synthesis

Identifiers

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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.