Incorporation o f stable isotopes 2H, 13C and 15N in the structure of azolo[5,1-c][l,2,4]triazines and azolo[1,5-a]pyrimidine as a tool for studying the chemical and biological transformations of nitrogenous heterocycles

Abstract

It is shown that selective incorporation of stable isotopes allows one to expand standard capabilities of NMR spectroscopy and is an effective approach to the study of the structure and reactivity of organic compounds. Azidotetrazole equilibrium, Dimroth rearrangement, and adamantylation of azoloazines were examined using compounds labeled by stable isotopes.