## Abstract The radiosyntheses of 5‐(4′‐[^18^F]fluorophenyl)‐uridine **[^18^F]‐11** and 5‐(4′‐[^18^F]fluorophenyl)‐2′‐deoxy‐uridine **[^18^F]‐12** are described. The 5‐(4′‐[^18^F]fluoro‐phenyl)‐substituted nucleosides were prepared via a Stille cross‐coupling reaction with 4‐[^18^F]fluoroiodobenzen
One-step, no-carrier-added, synthesis of a 18F-labelled benzodiazepine receptor ligand
✍ Scribed by Amir Reza Jalilian; Sayyed Abbas Tabatabai; Abbas Shafiee; Hossein Afarideh; Reza Najafi; Maria Bineshmarvasti
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- French
- Weight
- 336 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
To improve the accessibility of [18F]arylfluorides a method is presented using the decomposition of aromatic diazonium salts in the presence of [18F]fluoride. Several p-toluidyldiazonium salts have been synthesized and decomposed in the presence of fluoride. The most useful salt, ptoluidyldiazonium-
## Abstract [^18^F]Cholesteryl 4‐(fluoromethyl)benzoate **6b** was prepared from 3‐cholesteryl [(4‐nitrobenzenesulfonyl)oxymethyl]benzoate in one step using K^+^‐Kryptofix 2.2.2, as counter ion and acetonitrile as the solvent at 40–60°C. The product was isolated by HPLC in 75% (decay corrected) rad
## Abstract The synthesis of the [^3^H] labelled peripheral benzodiazepine receptor (PBR) ligand CB 34, useful for binding assay, tissue distribution studies, and elucidation of the physiological role of PBR, is described. Catalytic reduction with ^3^H~2~ gas and 10% Pd/C catalyst of the key interm