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• W3080513418 endingPage "4261" @default.
• W3080513418 startingPage "4254" @default.
• W3080513418 abstract "Abstract In this paper, a novel series of 2‐(4‐((1‐aryl‐1 H ‐1,2,3‐triazol‐4‐yl)methoxy)phenyl)2‐(2‐oxoazetidin‐1‐yl)acetamide derivatives are synthesized in two steps. The first step involved Ugi multicomponent reaction of β‐alanine, o ‐(propargyl)benzaldehyde and isocyanide derivatives. The product of this step, underwent a click 1,3‐dipolar cycloaddition reaction with benzyl azide derivatives. The 2‐(4‐((1‐aryl‐1 H ‐1,2,3‐triazol‐4‐yl)methoxy)phenyl)2‐(2‐oxoazetidin‐1‐yl)acetamide product was characterized and their antibacterial activities were evaluated against various G‐positive ( Staphylococcus aureus and Bacillus subtilis ) and G‐negative ( Pseudomonas aeruginosa and Escherichia coli ) bacteria, using minimal inhibition concentration. The compounds showed very good antimicrobial activity and a number of products have been more active than ciprofloxacin." @default.
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• W3080513418 date "2020-09-17" @default.
• W3080513418 modified "2023-09-27" @default.
• W3080513418 title "Design, synthesis and antibacterial activity evaluation of novel 2‐(4‐(( <scp> 1‐aryl‐1 <i>H</i> </scp> ‐1,2,3‐triazol‐4‐yl)methoxy)phenyl)2‐(2‐oxoazetidin‐1‐yl)acetamide derivatives" @default.
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• W3080513418 doi "https://doi.org/10.1002/jhet.4131" @default.
• W3080513418 hasPublicationYear "2020" @default.
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