A succinct synthesis of a new bicyclic y-lactam designed to possess antibacterial activity containing an oxazolidine ring is described.
Synthesis of a bicyclic γ-lactam dipeptide analogue
✍ Scribed by Jack E. Baldwin; Christopher Hulme; Alison J. Edwards; Christopher J. Schofield; Kevin E.B. Parkes
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- French
- Weight
- 257 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0040-4039
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Y-Lactam analogues of carbapenems have been synthesized using a [3+2] cyclisation approach. Slight antibiotic activity was observed in one case. S-Lactam antibiotics' mechanism of action involves active site acylation of key enzymes (penicillin binding proteins\_PBP's) required for bacterial cell wa
The synthesis of a Y-lactam analogue of the penems, which showed antibacterial activity, is described.
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