Green synthesis of pyrido[2,1‐ a ]isoquinolines and pyrido[1,2‐ a ]quinolins using Fe 3 O 4 ‐MNPs as efficient nanocatalyst: Study of antioxidant activity
Abstract 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 Fe 3 O 4 ‐MNPs with a...
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Published in | Journal of heterocyclic chemistry Vol. 57; no. 1; pp. 337 - 345 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2020
|
Online Access | Get full text |
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Summary: | Abstract
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 Fe
3
O
4
‐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 (Fe
3
O
4
‐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. |
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ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.3782 |