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Synthesis of S-[3H]-DO-710, a benzamide ligand of the D2-dopamine receptor and of S-[3H]-azidosulpride, its photoactivable analog

✍ Scribed by D. Rognan; A. Mann; P. Hamdi; C. C. Wermuth; P. Sokoloff; J. J. Schwartz; J. Roy; J. J. Morgat


Book ID
102375725
Publisher
John Wiley and Sons
Year
1987
Tongue
French
Weight
412 KB
Volume
24
Category
Article
ISSN
0022-2135

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✦ Synopsis


The p r e p a r a t i o n o f t h e t r i t i u m l a b e l l e d benzamides, S-[ 3 H 1-00-710 3 and S-[ H I -a z i d o s u l p r i d e i s reported. The synthesis i n v o l v e s enant i o s e l e c t i v e p r e p a r a t i o n o f t h e p y r r o l i d i n y l moiety, r e d u c t i v e t r i t i a t i o n o f an a l l y l i c precursor and conversion o f an amino, t o an azido f u n c t i o n .


πŸ“œ SIMILAR VOLUMES


Synthesis of [3H] aminocyclopropane carb
✍ Michael S. Dappen; Charles S. Markos; Christopher J. Gresk; Alex A. Cordi πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 French βš– 221 KB

## Abstract The synthesis of [^3^H] Aminocyclopropane carboxylic acid (ACC, 1) at high specific activity and high purity is described. The compound has been developed as a specific ligand for the Glycine‐B binding site.