## Abstract The synthesis of racemic [2‐^11^C]phenylglycine, starting with ^11^CO~2′~ is reported. The [^11^C]benzaldehyde, prepared as previsously described in a two‐step reaction from the corresponding [^11^C]benzoic acid salt, was used in a modified Bücherer‐Strecker reaction. The radiochemical
The synthesis of 2- [11C]-methylphenylalanine
✍ Scribed by A.D. Gee; B. Långström
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 159 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The title compound was ^11^C‐labelled in a one‐pot procedure using [^11^C]cyanogen bromide as the key intermediate. Synthesis time was 31–33 min counted from the end of bombardment, affording 1,3‐di(2‐tolyl)‐[^11^C]guanidine (6) in 87 % decay‐corrected radiochemical yield counted from [
## Abstract Levofloxacin, the pure S enantiomer of the fluoroquinolone antibiotic ofloxacin, was labeled via methylation of the corresponding, __des__‐methyl, secondary amine with N.C.A. [^11^C]methyl iodide. The methylation reaction was regioselective, giving predominantly the preferred methyl ami
## Abstract [^11^C]‐acetone, prepared from ^11^CO~2~ and methyllithium, was reduced to [^11^C]‐isopropanol. The latter reacted with methylphosphonic acid difluoride in the presence of diisopropylamine, to yield [11C]‐sarin. 3.4 GBq (100 mCi) of [^11^C]‐sarin may be obtained from about 55.5 GBq (1.