## S u in ma r y 1sN.15N-imidazoleacetic acid was synthesized from 15N, lSN-DL-histidine (>99 atom % 15N). The latter. oxidized with sodium hypochlorite. formed 15N.15N-imidazoleacetoniuile. The free acid was prepared after acid hydrolysis of the nitrile, elution from an anion exchange column with
Synthesis and NMR characterization of (15N)taurine [2-(15N)aminoethanesulfonic acid]
โ Scribed by G. Philippossian; D. H. Welti; R. Fumeaux; U. Richli; K. Anantharaman
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 282 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0022-2135
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โฆ Synopsis
The t i t l e compound was prepared i n three steps w i t h 55% overall y i e l d s t a r t i n g from potassium (lSN)phthal imide. The synthetic rout e involved reaction w i t h 1,2-dibromoethane, hydrolysis of the res u l t i n g N-(2-br0moethyl)(~~N)phtha7imide w i t h HBr and treatment of the 2-brom0ethyl(~~N)amine thus formed w i t h sodium sulphite. The product was characterized by 13C, ' H and "N NMR spectroscopy. The absolute coupling constants of I 5 N w i t h the
1 3 C nuclei and the non-exchanging protons were determined and an unambiguous assignment of the proton signals obtained.
๐ SIMILAR VOLUMES
The M y proton-coupled 15N NMR spectra of pyrimidine with natural isotope abundance and of bis-labelled [1,3-"N2]p~dine, obtained using single pulse experiments, are described. The "N and 'H spectra are analysed for "J, 'J and 4J(NH) as well as N,N and H,H coupling constants.
## Abstract The following substances have been synthesized and characterized as monomers or intermediates for syntheses of new polymers: 1โ(4โvinylbenzyl)uracil (**1a**), 1โ(4โvinylbenzyl)thymine (**1b**), __N__โ4โacetylโ1โ(4โvinylbenzyl)cytosine (**1c**), 1โ(4โvinylbenzyl)cytosine (**1d**), 9โ(4โv