作者:Paola Roveri、Vanni Cavrini、Rita Gatti、Fabrizio Bianucci、Paolo Legnani
DOI:10.1002/ardp.19823150409
日期:——
Starting from 5‐nitro‐2‐furoyl azide (1), some new 5‐nitro‐2‐furamides 2a–d, O‐alkyl N‐(5‐nitro‐2‐furyl)carbamates 3a,b and 5‐nitro‐2‐ureidofurans 4a,b were synthesized and tested for in vitro antimicrobial activity. Compounds 2c and 2d exhibited appreciable activity against S. pyogenes and S. aureus.
从5-硝基-2-呋喃酰叠氮化物(1)开始,一些新的5-硝基-2-呋喃酰胺2a-d,O-烷基N-(5-硝基-2-呋喃基)氨基甲酸酯3a、b和5-硝基-合成 2-脲基呋喃 4a、b 并测试其体外抗菌活性。化合物2c和2d对化脓性链球菌和金黄色葡萄球菌表现出可观的活性。