## Abstract (−)‐(__RS__)‐(__E__)‐3‐[(__6R,7R__)‐7‐((__Z__)‐2‐(5‐amino‐1,2,4‐thiadiazol‐3‐yl)‐2‐fluoromethoxyiminoacetamide]‐2‐carboxy‐8‐oxo‐5‐thia‐1‐azabicyclo[4.2.0]oct‐2‐ene‐3‐yl[‐2‐propenyl](carbamoylmethyl) ethylmethylammonium hydroxide inner salt (E1077), a new parenteral cephalosporin with we
Synthesis of 14C-labelled Cefluprenam (E1077), a novel parenteral cephalosporin antibiotic
✍ Scribed by Nobuaki Sato; Yasunobu Kai; G. I. Shemilt; Shigeru Chiku
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 214 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Cefluprenam (E1077) is a new parenteral cephalosporin with a well‐balanced antibacterial spectrum and potent antibacterial activity. It was synthesized labelled in the side chain at the 3‐position of the cephem with carbon‐14, starting from potassium [^14^C]cyanide, according to the method illustrated in Schemes 1,2. [^14^C]Cefluprenam having a specific activity of 3.9 MBq/mg, was obtained in 28.6 % overall radiochemical yield, with a radiochemical purity of more than 97.3 %.
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