2014
DOI: 10.1155/2014/619749
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Synthesis and Antimicrobial Activity of Some Novel Heterocyclic Candidates via Michael Addition Involving 4-(4-Acetamidophenyl)-4-oxobut-2-enoic Acid

Abstract: This paper discusses the utility of 4-(4-acetamidophenyl)-4-oxobut-2-enoic acid as a key starting material for the preparation of a novel series of pyridazinones, thiazoles derivatives, and other heterocycles via interaction with nitrogen, sulfur, and carbon nucleophiles under Michael addition conditions and studies the antimicrobial activities of some of these compounds.

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Cited by 6 publications
(4 citation statements)
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“…40 Another compound, €-2-methyl-5-((1S,2R,4R)-2-m ethyl-3-methylbocyclo[2,2,1]-heptane-2-yl)-pent-2-enoic acid was identified through NIST library, which showed promising antibacterial activity as mentioned in literature. 41 Third compound, identified through GC-MS, 3-(1-Benzyl-1Himidazol-2-yl)-5-methylisoxazole, is an aromatic aldehyde which also displayed antibacterial activity as per the report cited in literature. 42 These three compounds individually exhibit good antibacterial activity, however presence of these three compounds combinely in a single plant may increse its antibacterial activity.…”
Section: Zone Of Inhibition Of Negative Control (In Mm)mentioning
confidence: 76%
“…40 Another compound, €-2-methyl-5-((1S,2R,4R)-2-m ethyl-3-methylbocyclo[2,2,1]-heptane-2-yl)-pent-2-enoic acid was identified through NIST library, which showed promising antibacterial activity as mentioned in literature. 41 Third compound, identified through GC-MS, 3-(1-Benzyl-1Himidazol-2-yl)-5-methylisoxazole, is an aromatic aldehyde which also displayed antibacterial activity as per the report cited in literature. 42 These three compounds individually exhibit good antibacterial activity, however presence of these three compounds combinely in a single plant may increse its antibacterial activity.…”
Section: Zone Of Inhibition Of Negative Control (In Mm)mentioning
confidence: 76%
“…The infrared spectrum of the schiff base ligand has a broad absorption band at 3456 cm −1 which were due to the phenolic group [18,19]. The spectrum displays also medium band at 1290 cm −1 due to υ C-O (phenolic group) [20].…”
Section: Resultsmentioning
confidence: 99%
“…By careful comparison of the spectrum of the nano-metal complex with those of the Schiff base ligand, it was found that the band at 3456 cm −1 shifted to lower frequency region at 3401 cm −1 in the metal nano The IR spectrum of the ligand was compared with those of its metal complex to confirm the mode of bonding, as demonstrated in Table 3. The infrared spectrum of the schiff base ligand has a broad absorption band at 3456 cm −1 , which was due to the phenolic group [15,16]. The spectrum also displays medium band at 1290 cm −1 due to υ C-O (phenolic group) [17].…”
Section: Resultsmentioning
confidence: 99%
“…The infrared spectrum of the schiff base ligand has a broad absorption band at 3456 cm −1 , which was due to the phenolic group [ 15 , 16 ]. The spectrum also displays medium band at 1290 cm −1 due to υ C-O (phenolic group) [ 17 ].…”
Section: Resultsmentioning
confidence: 99%