Specifically labelled phenylacetic acid and mandelic acid derivatives, metabolites of L-Dopa, have been synthesized via the intermediary labelled benzyl alcohols, which were prepared by reduction of the methyl esters of the appropriate benzoic acids. The benzyl alcohols have been converted to the co
Synthesis of 1,2-dioleoyl-3-(α-14C-1-adamantoyl)-sn-glycerol and 1-14C-adamantanecarboxylic acid
✍ Scribed by Anthony J. Villani; Francis R. Pfeiffer
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 312 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The synthesis of 3‐indolylacetic acid labelled with ^14^C in side chain carbon atoms has been effected using (1‐^14^C)glycolic acid, (1,2‐^14^C~2~)glycolic acid and (2‐^14^C)glycolic acid in an yield of 40‐60%. Some of the parameters that affect the synthesis have been studied and the r
## Abstract 2‐__O__‐Arachidonoyl‐1‐__O__‐stearoyl‐__sn__‐glycerol is the most abundant molecular species of the 1,2‐diacyl‐__sn__‐glycerol signaling lipids in neural tissue. The facile preparation of 2‐__O__‐[1′‐^14^C]arachidonoyl‐1‐__O__‐stearoyl‐__sn__‐glycerol from 2‐__O__‐[1′‐^14^C]arachidonoyl
## Abstract A growing interest in the phytotoxic effects of trichloroacetic acid (TCA) has led us to develop a small‐scale (<1 mmol) one‐pot synthesis of [1,2‐^14^C]TCA with >70% yield and specific activity of 3.7 GBq/mmol. Copyright © 2001 John Wiley & Sons, Ltd.
Service der Ilol&culer )I.rqu&er CXN-SACLAY 91191 GIF-SUR-WETTE CEDKX M I SIII+UBY I The preparations of 1.~-bcnsiroxaso~e-3-.c.tic acid labelled with 14C in porition a o r B of the ride chain are dercribed. a-14C acid war obtained from 4-hydroxy cormrarin [3-14C] via Prier rearrangewnt of phenyl ac