Synthesis of phosphonate derivatives via Fe3O4/ZnO MNPs: Investigation of antioxidant ability

A novel and efficient procedure for the generation of quinazolinone phosphonate derivatives employing the reaction of euparin, isatin or its derivatives, primary amines, dialkyl acetylenedicarboxylates, trimethyl phosphite or triphenyl phosphite and acidic solution of hydrogen peroxide in aqueous media at ambient temperature under ultrasonic irradiation was developed. Without ultrasonic irradiation the reaction does not proceed and agitation of the reaction mixture is difficult. In addition, the power of some prepared compounds as antioxidant was studied using trapping of radical by 1,1-diphenyl-2-picrylhydrazyl (DPPH) and ferric reduction activity potential (FRAP) experiment. Some advantages of this procedure are: short time of reaction, high yields of product, easy isolation of products.

Authors

Publication Details

Published
2025-12-25
DOI
https://doi.org/10.82361/iranjoc.2025.1229449
Primary Topic
Phosphorus compounds and reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synthesis of phosphonate derivatives via Fe3O4/ZnO MNPs: Investigation of antioxidant ability

IAU
Phosphorus compounds and reactions
article

Synthesis of phosphonate derivatives via Fe3O4/ZnO MNPs: Investigation of antioxidant ability

IAU
article en

Abstract

A novel and efficient procedure for the generation of quinazolinone phosphonate derivatives employing the reaction of euparin, isatin or its derivatives, primary amines, dialkyl acetylenedicarboxylates, trimethyl phosphite or triphenyl phosphite and acidic solution of hydrogen peroxide in aqueous media at ambient temperature under ultrasonic irradiation was developed. Without ultrasonic irradiation the reaction does not proceed and agitation of the reaction mixture is difficult. In addition, the power of some prepared compounds as antioxidant was studied using trapping of radical by 1,1-diphenyl-2-picrylhydrazyl (DPPH) and ferric reduction activity potential (FRAP) experiment. Some advantages of this procedure are: short time of reaction, high yields of product, easy isolation of products.

Openalex Percentile: Top 32%
Phosphorus compounds and reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Synthesis of phosphonate derivatives via Fe3O4/ZnO MNPs: Investigation of antioxidant ability — IAU · (2025) | TGRS Research Map | TGRS