A process for preparing N-(substituted)-C-(substituted methyl)-oxazolidinones, C-(substituted methyl)-oxazolidinones, and N-(substituted)-C-(substituted methyl)-oxazolidinones, preferably chiral, from optically active C-(protected oxymethyl)-oxazolidinones is described. The process can be used to produce combinatorial libraries of the above substituted oxazolidinones in a two or three step reaction comprising a plurality of reagents differing in numbers of carbons or particular substituted oxazolidinones. A number of substituted oxazolidinones produced using the above process have been discovered to have antimicrobial activity.
本文介绍了一种从光学活性的C-(保护的
氧甲基)-
噁唑烷
酮制备N-(取代)-C-(取代
甲基)-
噁唑烷
酮、C-(取代
甲基)-
噁唑烷
酮和N-(取代)-C-(取代
甲基)-
噁唑烷
酮的方法,其中优选手性化合物。该方法可用于在包含多种
碳数或特定取代
噁唑烷
酮的多种试剂的两步或三步反应中产生上述取代
噁唑烷
酮的组合库。使用上述方法生产的许多取代
噁唑烷
酮已被发现具有抗微
生物活性。