Disclosed are compounds of the general formula: ##STR1## wherein R.sub.1 is amino, an acylated amino or a protected amino group, X is hydrogen or methoxy, and R' is hydrogen, R or R.sup.4 where R is an organic residue attached to the azetidine ring through a carbon atom therein and R.sub.4 is azido, a halogen, an amino group which may optionally be acylated or a group of the formula ##STR2## wherein R.sub.5 is an organic residue and n is 0, 1 or 2, and pharmaceutically acceptable salts and esters thereof. The compounds have antimicrobial and/or .beta.-lactamase-inhibitory activity and are of value as drugs for human beings and domesticated animals.
揭示了一般式为:##STR1## 的化合物,其中R.sub.1是
氨基、酰化
氨基或保护
氨基团,X是氢或甲氧基,R'是氢、R或R.sup.4,其中R是通过其中的一个碳原子连接到氮杂环的有机残基,R.sub.4是
叠氮基、卤素、可能被酰化的
氨基团或具有以下结构的团:##STR2## 其中R.sub.5是有机残基,n为0、1或2,以及其药学上可接受的盐和酯。这些化合物具有抗微
生物和/或β-内酰胺酶抑制活性,并且作为人类和家畜的药物具有价值。