2019
DOI: 10.1002/jhet.3714
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Synthesis, characterization & in vitro antimicrobial‐antioxidant studies of novel N,1‐diphenyl‐4,5‐dihydro‐1H‐1,2,4‐triazol‐3‐amine derivatives

Abstract: A new series of 1,2,4‐triazole was designed, synthesized, and characterized as remarkable antimicrobial and antioxidant agents. These heterocycles have been prepared from the cyclization reactions of Schiff bases 3(a‐k) with phenylhydrazine by refluxing under the alkaline medium. The Schiff bases in turn were realized in good yields from the condensation reactions of N‐phenylurea with different aromatic aldehydes. The structures of the intermediates 3(a‐k) and final heterocycles 4(a‐k) have been fully characte… Show more

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Cited by 7 publications
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“…Then, Yusuf and Thakur (2019) carried out the cyclization of several Schiff bases and phenylhydrazine by refluxing in an alkaline medium (KOH/EtOH mixture) with good yields affording novel 1,2,4-triazoles [ 110 ]. The precursor Schiff bases were prepared by condensation reactions of aromatic aldehydes with N -phenylurea using methanol as a solvent in an acid medium ( Scheme 45 ).…”
Section: Synthetic Methods For Highly Active Compounds Against Fox Speciesmentioning
confidence: 99%
“…Then, Yusuf and Thakur (2019) carried out the cyclization of several Schiff bases and phenylhydrazine by refluxing in an alkaline medium (KOH/EtOH mixture) with good yields affording novel 1,2,4-triazoles [ 110 ]. The precursor Schiff bases were prepared by condensation reactions of aromatic aldehydes with N -phenylurea using methanol as a solvent in an acid medium ( Scheme 45 ).…”
Section: Synthetic Methods For Highly Active Compounds Against Fox Speciesmentioning
confidence: 99%