Evidence map›Paper›PMID 42491416›Full record

ArticleRSC advances2026

M-NGO/UiO-66 nanocomposite: a green and efficient catalyst for the synthesis of 1,8-dioxodecahydroacridine derivatives.

Atefeh Zeinali, Leila Moradi

Abstract read
In one paragraph

Article in RSC advances, 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

2 authors.

Atefeh ZeinaliDepartment of Organic Chemistry, Faculty of Chemistry, University of Kashan P. O. Box 8731753153 Kashan I.R. Iran l_moradi@kashanu.ac.ir.
Leila MoradiDepartment of Organic Chemistry, Faculty of Chemistry, University of Kashan P. O. Box 8731753153 Kashan I.R. Iran l_moradi@kashanu.ac.ir.ORCID https://orcid.org/0000-0001-6830-907X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, a novel magnetic nanocomposite (M-NGO/UiO-66) was successfully synthesized. This nanocomposite was utilized as a green, heterogeneous, and recoverable catalyst in a one-pot pseudo-four-component reaction for the preparation of 1,8-dioxodecahydroacridine derivatives. The structure and physicochemical properties of the resulting nanocomposite were thoroughly characterized and confirmed using FT-IR, XRD, SEM, EDS, elemental mapping, BET, and VSM techniques. The catalytic performance of M-NGO/UiO-66 was evaluated under optimized reaction conditions, including 0.015 g of catalyst in ethanol at 80 °C, affording the target products within 8-25 min and in high yields ranging from 83% to 95%. The developed protocol demonstrates several significant advantages, such as operational simplicity, excellent catalytic activity, high atom economy, favorable reaction mass efficiency, utilization of a green solvent, and convenient magnetic recovery of the catalyst, making it an attractive and sustainable approach for the synthesis of acridine derivatives.

Identifiers

PMID42491416
PMCPMC13377563

What OpenQuestion holds

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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.