Institut deChimie desSubstancesNaturellesduCNRS-Gif/Yvette (S. et0.) \* Service des Molecules Marquees, C E N Saclay -BP. n02 -Gif/Yvette (S. et 0.) France Manuscrit regu le 1 decembre 1965 SUMMARY 5-Amino tetrazole 14C is prepared by action of cyanamide 14C on sodium azide in aqueous acid solution
Synthèse simplifiée de L'Acide Trans-Cinnamique 14C-3
✍ Scribed by M. Herbert; G. Rochas; L. Pichat
- Publisher
- John Wiley and Sons
- Year
- 1968
- Tongue
- French
- Weight
- 140 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Benzoic acid carboxyl 14C
(5 m M ) is reduced by LiAlH4 into benzyl alcohol 7-l". Oxidation of the latter by lead tetracetate in pyridine gives benzaldehyde J4CO which, without isolation is condensed with malonic acid. Cinnamic acid 3J4C is obtained with a 86 overall yield. Purified by sublimation, it is chromatographically homogenous in three solvent systems. Specific activity 10 mCilmM.
📜 SIMILAR VOLUMES
## Abstract Synthesis and chromatographic separation of (E) and (Z) isomers of [6‐^14^C] oxetorone : [6‐^14^C] 6‐(3‐Dimethylaminopropylidene)[2, 3‐e] benzofuro‐12H‐benzo [b] oxepin^\*^, hydrogen fumarate. A new synthesis of [6‐^14^C] oxetorone was devised allowing the three step preparation from ^1