𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Labeling of a serotoninergic ligand with 18F : [18F] setoperone

✍ Scribed by C. Crouzel; M. Venet; T. Irie; G. Sanz; C. Boullais


Publisher
John Wiley and Sons
Year
1988
Tongue
French
Weight
363 KB
Volume
25
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Labelling of a new serotoninergic ligand
✍ C. Crouzel; N. Venet; G. Sanz; A. Denis πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 French βš– 188 KB

SUI(IvLRY ## Ritanserin has been labelled with 18F to visualize the serotoninergic receptors by Positron Emission Tomography (PET). The synthesis was carried out by a nucleophilic substitution of a nitro substituent of a ni trophenylketone by 18F-and then addition of a Grignard reagent to the ket

Facile synthesis of N-succinimidyl 4-[18
✍ G. Tang; Wenbin Zeng; Meixiang Yu; G. Kabalka πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 French βš– 122 KB

## Abstract An efficient preparation of __N__‐succinimidyl 4‐[^18^F]fluorobenzoate ([^18^F]SFB) based on a convenient three‐step, one‐pot procedure is described. [^18^F]Fluorination of the precursor ethyl 4‐(trimethylammonium triflate)benzoate gave ethyl 4‐[^18^F]fluorobenzoate. Saponification of t

Synthesis of 18F-labelled biphenyls via
✍ BjΓΆrn Steiniger; Frank R. Wuest πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 French βš– 147 KB

The Suzuki reaction of organoboron compounds with 4-[ 18 F]fluoroiodobenzene has been developed as a novel radiolabelling technique in 18 F chemistry. The crosscoupling reaction of p-tolylboronic acid with 4-[ 18 F]fluoroiodobenzene was used to screen different palladium complexes, bases and solvent

The comparative synthesis of 18F-fluorop
✍ M. Murakami; K. Takahashi; Y. Kondo; S. Mizusawa; H. Nakamichi; H. Sasaki; E. Ha πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 French βš– 181 KB

Fluorination with 18F-F2 and 18F-AcOF were compared for the synthesis of 18F-fluorophenylalanines. L-phenylalanine in CF,COOH trapped 18F-AcOF more effectively than 18F-F2. The main product was ortho-18F-fluorophenylalanine when 18F-AcOF was used as a reagent. Lower radiochemical yield of 18F-fluoro