Abstract
The ß-lactam fused thiadiazine ylide (1) undergoes quantitative thermal rearrangement to the thiadiazine ring-opened ß-lactam (2), which can then undergo ß-lactam cleavage rections with a variety of nucleophilic reagents to give dipeptides [(3)-(5)].
| Original language | English |
|---|---|
| Pages (from-to) | 974-975 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 23 |
| DOIs | |
| Publication status | Published - 1974 |