Synthesis of selectively 13C-labelled benzoic acid for nuclear magnetic resonance spectroscopic measurement of glycine conjugation activity
✍ Scribed by Kazuki Akira; Hiroshi Hasegawa; Shigeo Baba
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 435 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The synthesis of [4‐^13^C]benzoic acid (BA) labelled in a single protonated carbon, for use as a probe to measure glycine conjugation activity by nuclear magnetic resonance (NMR) spectroscopy, has been reported. The labelled compound was prepared by a seven‐step synthetic scheme on a relatively small scale using [2‐^13^C]acetone as the source of label in overall yield of 16 %. The usefulness of [4‐^13^C]BA was demonstrated by the NMR spectroscopic monitoring of urinary excretion of [4‐^13^C]hippuric acid in the rat administered with the labelled BA.
📜 SIMILAR VOLUMES
A detailed structural analysis of the copolyesterification in bulk without any external catalyst at 160ЊC between o-phthalic anhydride (P), oleic acid (O), and trimethylolpropane (T) with a mol ratio ([{COOH]/[{OH]) Å 0.70 has been carried out by high resolution 13 C nuclear magnetic resonance ( 13