Oxazolidinones and methods for their synthesis are provided. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. Oxazolidinones as disclosed herein can be readily synthesized and used in a variety of applications including use as antimicrobial agents. In one embodiment, a variety of thioamidomethyloxazolidinones and methods for their synthesis and use are provided.
本发明提供了
噁唑烷酮及其合成方法。还提供了制备
生物活性
噁唑烷酮的方法,以及包含
噁唑烷酮的药学可接受组合物的方法。本发明所披露的
噁唑烷酮可以很容易地合成,并可用于各种应用,包括用作抗微
生物剂。在一种实施例中,提供了各种
硫代酰胺甲基
噁唑烷酮及其合成和使用方法。