Green synthesis of pyridoisoquinolines and pyridoquinolins using Fe3O4‐MNPs as efficient nanocatalyst: Study of antioxidant activity

In this work, synthesis of pyrido[2,1‐a]isoquinolines and pyrido[1,2‐a]quinolins in excellent yield using multicomponent reaction of phthalaldehyde, methyl amine, methyl malonyl chloride, alkyl bromides, and triphenylphosphine in the presence of catalytic amount of Fe3O4‐MNPs with aqueous sodium hyd...

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Bibliographic Details
Published inJournal of heterocyclic chemistry Vol. 57; no. 1; pp. 337 - 345
Main Authors Naghmeh Faal Hamedani, Ghazvini, Maryam, Azad, Leila, Annataj Noushin
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc 01.01.2020
Subjects
Antioxidants
Bromides
Ferric chloride
Ferric ions
Iron chlorides
Iron oxides
Nanoparticles
Sodium hydroxide
Synthesis
Trapping
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Summary:In this work, synthesis of pyrido[2,1‐a]isoquinolines and pyrido[1,2‐a]quinolins in excellent yield using multicomponent reaction of phthalaldehyde, methyl amine, methyl malonyl chloride, alkyl bromides, and triphenylphosphine in the presence of catalytic amount of Fe3O4‐MNPs with aqueous sodium hydroxide at 80°C was investigated. The reduction of ferric chloride solution with Clover Leaf water extract caused to synthesis of magnetic iron oxide nanoparticles (Fe3O4‐MNPs) as a green method. As well, antioxidant activity was studied for the some newly synthesized compounds such as 6a, 6c, 9b, and 9c using the DPPH radical trapping and reducing of ferric ion experiments and comparing results with synthetic antioxidants (TBHQ and BHT). As a result, compounds 6a, 6c, 9b, and 9c show good DPPH radical trapping and excellent reducing strength of ferric ion.
ISSN:0022-152X
1943-5193
DOI:10.1002/jhet.3782