Abstract
Several polycyclic β-lactams have been synthesized by the reactions of cyclic imines with acid chlorides in the presence of triethylamine. The azido-functions in these β-lactams were reduced to amino-groups, which were then acylated with phenylacetyl chloride to introduce the penicillin G side chain. Some carbocyclic analogues of cephalosporin were found to possess antibacterial activity.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2193-2197 |
| Number of pages | 5 |
| Journal | Journal of the Chemical Society, Perkin Transactions 1 |
| Issue number | 20 |
| DOIs | |
| State | Published - 1976 |
All Science Journal Classification (ASJC) codes
- General Chemistry