Design and Synthesis of Antimicrobial Active New Molecular Entities of N-Substituted Pipradol Derivatives

摘要

Synthesis of antimicrobial 4-(hydroxyldiphenyl methyl)piperidin-l-yl)(substituted phenyl)methanone derivatives by using conventional chemical reactions to produces feasible and entirely new chemical entities (NCE'S) which were having a great potential microbial activities equivalent to fexofenidine used as a biological standard. This invention may help full for derive more potential pipradol molecules with peptide bond linkage.