of antibacterial activity for certain analogs is proposed. The successful use of organo-cadmium reagents for the synthesis of the aliphatic and aromatic series of α- as well as β-amino ketones indicates a wider scope of applicability than by the method of Dakin-West or by Friedel-Crafts acylation. These series of compounds show antimicrobial activity in vitro.
合成了
氨基酸的α-和β-
氨基
酮类似物,作为微
生物代谢中
氨基酸的潜在拮抗剂。提出了某些类似物的抗菌活性的假想机理。与Dakin-West方法或Friedel-Crafts酰化方法相比,成功地将有机
镉试剂成功用于脂族和芳族系列的α-以及β-
氨基酮的合成表明其适用范围更广。这些系列的化合物在体外显示出抗菌活性。