2019
DOI: 10.1016/j.bmcl.2019.126636
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Heterocyclic β-keto sulfide derivatives of carvacrol: Synthesis and copper (II) ion reducing capacity

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Cited by 7 publications
(2 citation statements)
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“…Initial protection of the hydroxyl group of thymol was accomplished by its reaction with iodomethane in the presence of bicarbonate to afford methoxythymol (2) [54]. Subsequently, 4-acetylmethoxythymol (3) was obtained by acylation of 2 applying Friedel-Crafts conditions [55], followed by a condensation of 3 with the corresponding thiosemicarbazide under reflux and a catalytic amount of AcOH in ethanol to provide thiosemicarbazones 4a-b [56].…”
Section: Synthesismentioning
confidence: 99%
“…Initial protection of the hydroxyl group of thymol was accomplished by its reaction with iodomethane in the presence of bicarbonate to afford methoxythymol (2) [54]. Subsequently, 4-acetylmethoxythymol (3) was obtained by acylation of 2 applying Friedel-Crafts conditions [55], followed by a condensation of 3 with the corresponding thiosemicarbazide under reflux and a catalytic amount of AcOH in ethanol to provide thiosemicarbazones 4a-b [56].…”
Section: Synthesismentioning
confidence: 99%
“…The presence of hydroxyl group (OH) in carvacrol is the major reason for its radical scavenging activity (superoxide radicals, nitric oxide, and hydrogen peroxide). Its weak acid character facilitates hydrogen atoms donation to unpaired electrons, making another radical stabilized by electron scattering produced at molecule resonance structure (Cocolas et al, 2019 ; Mir et al, 2020 ). Carvacrol protects against oxidative stress made by restraint stress damages the brain, liver, and kidney.…”
Section: Therapeutic Perspectivesmentioning
confidence: 99%