𝔖 Bobbio Scriptorium
✦   LIBER   ✦

(3 R ,4 S )-3-[4-(4-Fluorophenyl)-4-hydroxypiperidin-1-yl]chroman-4,7-diol: A Conformationally Restricted Analogue of the NR2B Subtype-Selective NMDA Antagonist (1 S ,2 S )-1-(4-Hydroxyphenyl)-2- (4-hydroxy-4-phenylpiperidino)-1-propanol

✍ Scribed by Butler, Todd W.; Blake, James F.; Bordner, Jon; Butler, Paul; Chenard, Bertrand L.; Collins, Mary A.; DeCosta, Debra; Ducat, Mary J.; Eisenhard, Michael E.; Menniti, Frank S.; Pagnozzi, Martin J.; Sands, Steven B.; Segelstein, Barbara E.; Volberg, Walter; White, W. Frost; Zhao, Dayao


Book ID
127100419
Publisher
American Chemical Society
Year
1998
Tongue
English
Weight
263 KB
Volume
41
Category
Article
ISSN
0022-2623

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Synthesis of N- Substituted 4-(4-Hydroxy
✍ Guzikowski, Anthony P.; Tamiz, Amir P.; Acosta-Burruel, Manuel; Hong-Bae, Soo; C πŸ“‚ Article πŸ“… 2000 πŸ› American Chemical Society 🌐 English βš– 337 KB

Antagonists at the 1A/2B subtype of the NMDA receptor (NR1A/2B) are typically small molecules that consist of a 4-benzyl-or a 4-phenylpiperidine with an Ο‰-phenylalkyl substituent on the heterocyclic nitrogen. Many of these antagonists, for example ifenprodil (1), incorporate a 4-hydroxy substituent

Preparation of carbon-14 labeled (3R)-7-
✍ Bertold D. Berrang; Anita H. Lewin; F. Ivy Carroll πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 French βš– 128 KB πŸ‘ 1 views

## Abstract Starting with [^14^C]‐D‐tyrosine, carbon‐14 labeled JDTic dihydrochloride with specific activity 15 mCi/mol was prepared in 5% radiochemical yield. Separation of the (3__R__)‐ and (3__S__)‐diastereomers was carried out via the 3‐phenyl‐2,3,10,10a‐tetrahydro‐5H‐imidazo[1,5‐b]isoquinolin‐