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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.


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