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Fujisaki, Fumiko; Hiromatsu, Sachi; Matsumura, Yumiko; Fukami, Aki; Kashige, Nobuhiro; Miake, Fumio; Sumoto, Kunihiro
Journal of heterocyclic chemistry, 03/2013, Letnik: 50, Številka: 2Journal Article
In connection with our studies on antibacterial active compounds in the class of new oxazolidinones against Gram‐positive (Staphylococcus aureus) and Gram‐negative (Escherichia coli) strains, some molecular modifications were attempted. In this study, molecular modifications of 4‐aminomethyloxazolidin‐2‐ones (3a) to the corresponding 4‐acylaminomethyloxazolidin‐2‐one derivatives (3c–d) and preparations of the represented twin‐drug type molecules (10–14) were investigated. Some additional 4‐dialkylaminomethyloxazolidin‐2‐ones (2) were also synthesized. The synthesized compounds were evaluated for antibacterial activity with Gram‐positive (S. aureus) and Gram‐negative (E. coli) strains.
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