Design, synthesis and biological activity of novel enediynyl monocyclic β-lactams
作者:Amit Basak、Uttam Kumar Khamrai
DOI:10.1016/0040-4039(96)00297-3
日期:1996.4
Monocyclic β-lactams 1–3 substituted at C-4 with enediyne moiety have been synthesized via Pd(0) mediated coupling reaction. Their antibacterial activity against ampicillin-resistant E. coli have been tested.
通过Pd(0)介导的偶联反应合成了在C-4处被烯二炔部分取代的单环β-内酰胺1-3。已经测试了它们对耐氨苄青霉素的大肠杆菌的抗菌活性。