Reactions of 3-formylchromone with active methylene and methyl compounds and some subsequent reactions of the resulting condensation products.

Renata Gasparová, Margita Lácová

Abstract read

In one paragraph

Article in Molecules (Basel, Switzerland), 2005. 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

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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.

Recyclization of morpholinochromonylidene-thiazolidinone using nucleophiles: facile synthesis, cytotoxic evaluation, apoptosis, cell cycle and molecular docking studies of a novel series of azole, azine, azepine and pyran derivatives.RSC advances · 2023
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.

Renata GasparováDepartment of Chemistry, Faculty of Natural Sciences, University of St. Cyril and Methodius, Slovak Republic. renata.gasparova@ucm.sk

Margita Lácová

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review presents a survey of the condensations of 3-formylchromone with various active methylene and methyl compounds, e.g. malonic or barbituric acid derivatives, five-membered heterocycles, etc. The utilisation of the condensation products for the synthesis of different heterocyclic systems, which is based on the ability of the gamma-pyrone ring to be opened by the nucleophilic attack is also reviewed. Finally, the applications of microwave irradiation as an unconventional method of reaction activation in the synthesis of condensation products is described and the biological activity of some chromone derivatives is noted.

Indexed as

Models, ChemicalAcetatesAcetonitrilesBarbituratesBenzoatesChromonesDinitrobenzenesDioxanesGlycineHeterocyclic CompoundsHippuratesHydrocarbonsPentanonesPhenylacetatesPropionatesQuinonesAcetatesAcetonitrilesaceturic acidacetylacetoneBarbituratesbarbituric acidBenzoatesbenzoylpropionic acidChromonesDinitrobenzenesDioxanesethyl acetateformylchromoneGlycineHeterocyclic CompoundsHippurateshippuric acidHydrocarbonsMeldrum's acidPentanonesPhenylacetatesphenylacetic acidPropionatesQuinonesSulfonesThiazoles

Identifiers

PMID18007363

DOI10.3390/10080937

PMCPMC6147603

What OpenQuestion holds

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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.