Synthesis of (β-methyl3H-6β-iodopenicillanic acid
✍ Scribed by Fabien De Meester; Jean-Marie Frère; Jean-Louis Piette; Hubert Vanderhaeghe
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- French
- Weight
- 428 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
A rapid and easy synthesis of tritium-labelled 8-iodopenicillanate, an efficient inactivator of serine B-lactamase, is described. This method involves only three reaction steps after the introduction of the label in the molecule with an overall yield of 16 % .
📜 SIMILAR VOLUMES
## Abstract We have synthesized β‐aminoisobutyric acid (3‐amino‐2‐[^3^H]methyl‐propanoic acid) and β‐ureidoisobutyric acid (3‐[(aminocarbonyl)amino]‐2‐[^3^H]methyl‐propanoic acid) starting with [^3^]thymidine (1‐(2‐deoxy‐β‐D‐ribo‐furanosyl)‐5‐[^3^H]methyluracil). We have developed a simplified enzy