Labelling of leukotrienes with isotopes (14C, 2H, 3H) or with a non isotopically labelled Fe(CO)3 group: Syntheses and utilisations
✍ Scribed by J.P. Beaucourt
- Book ID
- 103920271
- Publisher
- Elsevier Science
- Year
- 1988
- Weight
- 40 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0883-2889
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract In support of a program to develop a treatment for depression, three isotopically labeled forms of the 5‐HT~1B~ antagonist AZ12320927 were synthesized. A tritium labeled version was synthesized for autoradiography using Ir‐catalyzed hydrogen–tritium exchange. A C‐14 labeled version was
A m s t e r d a m -THE NETHERLANDS. R e c e i v e d on November 3. 1 9 7 0 . SUMMARY P r o c e d u r e s a r e g i v e n f o r t h e p r e p a r a t i o n of ( 2 -" C / , I?-' H I n a p h t h a l e n e , ( 1 -' C / , I ?-3 H I n a p h t h a l e n e , I. 2.3.4t e t r a h y d r o -( Z -" C ) , ( ? -'
## Abstract 5‐Fluoro‐1,3‐dihydro‐1‐hydroxy‐2,1‐benzoxaborole (AN2690) is a new antifungal agent for the potential treatment of onychomycosis. During the preclinical development phase, it was necessary to synthesize the radioisotope [3‐^14^C]‐5‐fluoro‐1,3‐dihydro‐1‐hydroxy‐2,1‐benzoxaborole and the