Author:
Sedlák Miloš,Halama Aleš,Kaválek Jaromír,Macháček Vladimír,Mitaš Petr,Štěrba Vojeslav
Abstract
A series of 11 substituted 2-(4-nitrophenyl)imidazolinones have been prepared by base catalyzed cyclizations of substituted 2-(4-nitrobenzoylamino)alkanamides. At higher methoxide concentrations the cyclization can be accompanied by reduction of nitro group to azoxy group. All the substances prepared have been identified by 1H and 13C NMR spectra.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
14 articles.
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