Author:
Marchalín Miroslav,Světlík Jan,Martvoň Augustin
Abstract
Addition-cyclization reactions of 2-pyridyl isothiocyanate with enamines and C-acids afforded derivatives containing pyrido[1,2-a]pyrimidine skeleton. Cyclization with a series of phenylhydrazones gave substituted triazolidines. The IR, UV, 1H NMR and 13C NMR spectra of the synthesized compounds are discussed.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
16 articles.
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