## Abstract A synthetic procedure for C‐14‐labeled N‐methyl‐N‐nitrosoaniline is presented. Separate labeling of the methyl and phenyl side chains was achieved by using C‐14‐labeled methyl iodide and aniline, respectively. The overall yield of the four reactions was 62% and the final products were s
Synthesis of ring 14C-methyl labeled retinyl acetate
✍ Scribed by William T. Colwell; Caroline Soohoo; Joseph I. Degraw
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- French
- Weight
- 267 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A method for incorporation of a ^14^C‐label in the ring geminal methyl moiety of Vitamin A is described. The procedure involves mono methylation of 2,6‐dimethylcyclohexanone with ^14^C‐methyl iodide as catalyzed by potassium hydride to afford 2‐^14^C, 2,6‐trimethylcyclohexanone. Subsequent condensation with an 11‐carbon acetylenic side chain, followed by reduction, acetylation and dehydration yielded ^14^C‐retinyl acetate. Final purification was achieved by preparative thin layer chromatography.
📜 SIMILAR VOLUMES
## Abstract Methyl sterculate, a cyclopropenoid fatty acid, has been synthesized with carbon‐14 as the methylene carbon in the cyclopropene ring.
Synthesis o f specific labelled [methyl-14Clsarin. The synthesis of label led [methyl-14Clsarin, [14Clmethylphosphonofluoridic acid 1-methylethyl ester, was accomplished by another approach as for nonlabelled sarin in a tele-conducted reaction vessel. The purity was estimated by IR, GC, and GC-MS a
## Abstract p‐Toluic acid‐ring‐^14^C was synthesized by the Friedel‐Crafts p‐carbamylation of toluene‐ring‐^14^C with N,N‐disubstituted carbamyl chloride and subsequent hydrolysis. The radiochemical yield was 61%. An attempt was made to apply this method for the synthesis of benzoic acid‐ring‐^14^C