## Abstract Diazepam‐^14^C and demethyldiazepam‐^14^C are synthesized from glycine‐1‐^14^C. Addition of diketene to diazepam‐^14^C leads to ketazolam‐^14^C. The reaction conditions for the formation of ketazolam from diazepam is studied using high‐pressure liquid chromatography in conjunction with
Synthesis of carbon-14 labeled [1-14C]-, and [2-14C]-L-tyrosine
✍ Scribed by W. Augustyniak; R. Kański; M. Kańska
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- French
- Weight
- 96 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.483
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✦ Synopsis
Abstract
Two labeled isotopomers of L‐tyrosine, L‐Tyr, have been synthesized using specific properties of the enzymes phenylanine ammonia lyase, PAL, and L‐phenylalanine hydroxylase. In an intermediate step [1‐^14^C]‐, and [2‐^14^C]‐L‐phenylalanine, L‐Phe, have been obtained from [1‐^14^C]‐, and [2‐^14^C]cinnamic acid, prepared from potassium [^14^C]cyanate or [2‐^14^C]malonic acid, and by addition of ammonia in the presence of enzyme PAL. The labeled isotopomers of L‐Phe have been converted into [1‐^14^C]‐, and [2‐^14^C]‐L‐Tyr using the enzyme L‐phenylalanine hydroxylase. Copyright © 2001 John Wiley & Sons, Ltd.
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