2015
DOI: 10.1016/j.jtusci.2014.08.001
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Synthesis, spectral characterization of some new 3-heteroaryl azo 4-hydroxy coumarin derivatives and their antimicrobial evaluation

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Cited by 72 publications
(28 citation statements)
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“…Many coumarins are synthesized in the lab and used as medicines for humans and animals. In this sense, coumarin-1,2,3triazole conjugate and 3-heteroarylazo 4-hydroxy showed bactericidal action against Enterococcus faecalis [80] and Staphylococcus aureus, Escherichia coli, Bacillus subtilis, and Pseudomonas aeruginosa [69], respectively ( Table 1).…”
Section: Coumarinsmentioning
confidence: 98%
“…Many coumarins are synthesized in the lab and used as medicines for humans and animals. In this sense, coumarin-1,2,3triazole conjugate and 3-heteroarylazo 4-hydroxy showed bactericidal action against Enterococcus faecalis [80] and Staphylococcus aureus, Escherichia coli, Bacillus subtilis, and Pseudomonas aeruginosa [69], respectively ( Table 1).…”
Section: Coumarinsmentioning
confidence: 98%
“…Many authors have published researches exploring the medicinal properties of coumarins [4,6,12,[35][36][37]. Coumarins possess antimicrobial activity such as antibacterial [38][39][40][41][42][43][44] and antifungal [40,[45][46][47][48]. Numerous coumarin derivatives showed significant antioxidant activity [49][50][51][52][53].…”
Section: Introductionmentioning
confidence: 99%
“…Further reactions were carried out between various phenol derivatives and ethyl 3,3-diethoxypropionate afforded products in poor to high yields (< 5-90%). Sahoo et al reported synthesis of 4-hydroxy-3-(hetero aryl Azo) coumarins [43]. Initially, 4hydroxy coumarin was synthesized via Claisen condensation of 2-hydroxy acetophenone and diethyl carbonate, in the presence of sodium hydride in toluene.…”
mentioning
confidence: 99%
“…It had been reported that azo‐ compounds exhibit interesting biological activities such as in‐vitro antimicrobial activity. [ 3 ] In general, azo‐ compounds exhibit good antibacterial activity against Gram‐positive bacteria such as Staphylococcus aureus but they are inactive against Gram‐negative bacteria such as Pseudomonas aeruginosa . [ 4 ] This behavior is attributed to the structural similarity of azo‐ compounds with stilbenes, and so, they could share the same mechanism of action.…”
Section: Introductionmentioning
confidence: 99%