Forty‐eight chalcone analogs were synthesized and their in vitro antibacterial activity
against Staphylococcus aureus NCIM 5021, Bacillus subtilis NCIM 2718, Phaseolus vulgaris …

The antibacterial activity of 31 chalcones was tested against bacterial strains, Bacillus
cereus ATCC 11778, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC …

A series of simple heterocyclic chalcone analogues have been synthesized by Claisen
Schmidt condensation reactions between substituted benzaldehydes and heteroaryl methyl …

In this study, novel series of chalcone derivatives, namely, 4-[4-(3-phenyl-acryloyl)-
phenylamino]-chromen-2-one (5a–k) have been synthesized from the intermediate 4-(4 …

A total of 30 chalcone analogues was synthesized via a base catalyzed Claisen Schmidt
condensation and screened for their in vitro antibacterial activity against Methicillin-sensitive …

Chalcones are open-chain flavonoids which contains two aromatic rings are joined by 3-
carbons α-, β-unsaturated carbonyl chain. The, β-unsaturated ketonic group which is liable …

Chalcones, containing an α, β-unsaturated ketone fragment, are an important
pharmacologically active agents because of their diverse mechanisms. This review provides …

A large series of chalcones were synthesized and studied against Staphylococcus aureus
and Escherichia coli. Chalcones were either unsubstituted in ring A or possessed 4′-chloro …

Three novel series of chalcone derivatives containing an aminoguanidine or acylhydrazone
moiety were designed, synthesized and evaluated in terms of their antibacterial, antifungal …

A series of 25 new chalcones were synthesized by Claisen‐Schmidt condensation, well
characterized by spectroscopic data, and evaluated for their antibacterial and antifungal …