Abstract
β-Lactam reacts with hetero nucleophiles under ring cleavage to give 2,2-dimethyl-3-oximinobutanoic esters 6 and 7 . N-hydroxyazetidine 5 , the precursor of β-lactam 1, is prepared by a new method.
| Original language | Undefined |
|---|---|
| Pages (from-to) | 2809-2812 |
| Journal | Tetrahedron letters |
| Volume | 26 |
| Issue number | 23 |
| DOIs | |
| Publication status | Published - 1985 |
Keywords
- IR-69457
Cite this
van Elburg, P. A., Reinhoudt, D., Harkema, S., & van Hummel, G. J. (1985). 1,4-diacetoxy-β-lactams. Reactions with nucleophiles. Tetrahedron letters, 26(23), 2809-2812. https://doi.org/10.1016/S0040-4039(00)94918-9