SYNTHESIS OF ISOTOPICALLY-LABELED NITROXYL RADICALS FOR USE AS SPIN PROBES

Citation
R. Bolton et al., SYNTHESIS OF ISOTOPICALLY-LABELED NITROXYL RADICALS FOR USE AS SPIN PROBES, Journal of labelled compounds & radiopharmaceuticals, 34(7), 1994, pp. 663-668
Citations number
4
Categorie Soggetti
Chemistry Analytical","Pharmacology & Pharmacy
ISSN journal
03624803
Volume
34
Issue
7
Year of publication
1994
Pages
663 - 668
Database
ISI
SICI code
0362-4803(1994)34:7<663:SOINRF>2.0.ZU;2-#
Abstract
The synthesis of [N-15]-1,1,1,1,3, 3-tetrakis(trideuteriomethyl)isoind olin- and of some 5-alkyl derivatives have been achieved by standard s ynthetic routes.(1) The presence of deuterium improves the sharpness o f the signals, and this, together with the incorporation of nitrogen-1 5, enhances the application of such compounds as spin probes; alkyl su bstituents at C-5 improve the lipophilicity.