## Abstract The work presented illustrates a practical sequence requiring relatively simple and inexpensive aoparatus, and using the commercially available isotopic sources, to produce L‐alanine from M+3 (^13^C~2~, ^15^N) to M+12 (^13^C~3~, ^15^N, D~4~, ^18^O~2~).
Synthesis of multilabeled histidine
✍ Scribed by Caroline Soohoo; John A. Lawson; Joseph I. Degraw
- Book ID
- 102369946
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- French
- Weight
- 244 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The synthesis of tetralabeled histidine 15 described. Glycine‐^15^N was converted essentially by literature procedures to 4‐chloromethylimidazole‐3‐^15^N‐2,5‐^2^H~2~. Alkylation of ethyl acetamidocyanoacetate‐2‐^13^C, followed by acid hydrolysis and decarboxylation yielded DL‐histidine‐α‐ ^13^C‐3‐^15^N‐2,5‐^2^H~2~. The compound is useful as a mass spectrometric standard for the measurement of histidine and metabolites in biological media.
📜 SIMILAR VOLUMES
## Abstract ^18^O‐multilabeled anhydrous nitric acid (89 atom % ^18^O) was prepared by exchange with H~2~^18^O, neutralization with NH~3~, and distillation from methane sulfonic acid. The use of trifluoromethane sulfonic acid, sulfuric acid, and oleum was also investigated, but these acids were fou
## Abstract 5‐[4‐^13^C,^15^N]‐ and 5‐[5‐^13^C,^15^N]Aminolevulinic acid (ALA) were simply synthesized in four steps by the condensation of [1‐^13^C,^15^N]‐ or [2‐^13^C,^15^N]glycine, respectively, with phthalic anhydride, followed by conversion to the chloride, coupling reaction with a three‐carbon