2011
DOI: 10.3109/14756366.2011.555944
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Synthesis and biological evaluation of fused oxepinocoumarins as free radicals scavengers

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Cited by 17 publications
(8 citation statements)
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“…The resulting white solid was filtered and purified by column chromatography on silica gel with petroleum ether/ethyl acetate (8:1, v/v) as eluent to afford 2 (1.85 g, 86%). Mp: 100‐101°C (literature value: 103‐104°C) . IR (KBr pellet) ν = 3464, 1726, 1624, 1560, 1397, 1274, 1145, 1066, 935, 843 cm –1 .…”
Section: Methodsmentioning
confidence: 98%
“…The resulting white solid was filtered and purified by column chromatography on silica gel with petroleum ether/ethyl acetate (8:1, v/v) as eluent to afford 2 (1.85 g, 86%). Mp: 100‐101°C (literature value: 103‐104°C) . IR (KBr pellet) ν = 3464, 1726, 1624, 1560, 1397, 1274, 1145, 1066, 935, 843 cm –1 .…”
Section: Methodsmentioning
confidence: 98%
“… In the course of our interest on the synthesis of fused pyridocoumarin derivatives, we wish to report here the application of FeCl 3 catalysis in the synthesis of the title compounds by using the three‐component domino reactions with aminocoumarins, benzaldehyde, and phenylacetylene. On the basis of our previous experience on the antioxidant and antilipid peroxidation properties of coumarin derivatives, we screened the synthesized compounds in vitro for their antioxidant profile. The reactions studied and the products obtained are depicted in Schemes and .…”
Section: Introductionmentioning
confidence: 99%
“…The reactions studied and the title new compounds received are depicted in Schemes ( 1 - 5 ). The nitrile oxide, generated from the oxime 2a [ 18 ] by chlorination with NCS in DMF solution followed by addition of Et 3 N in an one-pot procedure, was treated with the allyloxycoumarin 3a [ 19 ] under stirring for 24 h and Ar atmosphere (Scheme 1 ) to give the isoxazoline 4a in 68% yield (Table 1 , entry 1). The isoxazoline 4a has the expected regiochemistry [ 18 ] as indicated by HMBC experiments.…”
Section: Resultsmentioning
confidence: 99%