Bicyclic imidazolidinones as potential antibiotics
✍ Scribed by Jacqueline Marchand-Brynaert; Huguette Vanlierde; Léon Ghosez
- Book ID
- 102773551
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 858 KB
- Volume
- 97
- Category
- Article
- ISSN
- 0037-9646
No coin nor oath required. For personal study only.
✦ Synopsis
The bicyclic imidazolidinones 5 topologically related to the penicillin family, are susceptible to form a stable carbamate with serine-D,D-peptidases. A series of N-7 acylated or sulfonylated (2R, 5R)-3,3-dimethyl-8-oxo-4-thia-7,l -diazabicyclo[3.3.0]octane-2-carboxylates 2-a have been prepared. None of these novel penicillin analogs exhibited antibacterial activity.
📜 SIMILAR VOLUMES
racemic compounds 19a-c, prepared in six steps from 5-oxohydantoin, were inactive onto bacterial tests. The 5-acylamino-3-acetylhydantoin derivatives 8 were designed as potential antibiotics mimicking lactivicin 1. The