## 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
The synthesis of 18O multilabeled anhydrous nitric acid
✍ Scribed by A. C. Scott; J. H. McReynolds; M. Anbar
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- French
- Weight
- 170 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
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 found unsuitable due to rapid oxygen exchange. The extent of exchange was. monitored by converting water to methanol, nitric acid to nitroanisole, and analyzing by field ionization mass spectrometry.
📜 SIMILAR VOLUMES
## 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~).
A method is described for the preparation of concentrated solutions (50–70%) of ^18^O‐labelled H~2~O~2~ in water. All singly ^2^H‐, ^13^C‐ and ^18^O‐labelled species of peroxyformic acid have been synthesized by the reaction of appropriately labelled formic acid and H~2~O~2~.
## Abstract 3‐Chloroperbenzoic acid‐^17^O,^18^O was prepared from 3‐chlorobenzoyl chloride and hydrogen peroxide‐^17^O,^18^O (obtained by subjecting water‐^17^O,^18^O. Nitrobenzene‐^15^N was reduced to aniline‐^15^N, which was oxidised by 3‐chloroperbenzoic acid to nitrosobenzene‐^15^N. ^15^N and ^