Author:
Kurfürst Antonín,Schwarz Marián
Abstract
Nitration of polyalkyated 3,5-dicyano-1,4-dihydropyridines Ia-Id to the first and second degrees has been studied leading to compounds II and III, and conversion of nitromethyl groups of these compounds into nitrile groups with formation of tricyano derivatives IV and tetracyano derivatives V has been followed. Also given is the fragmentation of the synthesized compounds II-V by an electron impact in mass spectrometer and further spectral characteristics.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
5 articles.
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1. One-pot nitrodebromination and methyl bi-functionalization of 5-bromo 6-methylpyrimidines: a unique simultaneous transformation;Monatshefte für Chemie - Chemical Monthly;2020-07-24
2. An overview of the retro-Diels-Alder reaction in semiunsaturated heterocyclic rings: mass spectra of new substituted 1,4,5,6,7,8-hexahydroquinolines and their oxo-analogues 5,6,7,8-tetrahydro-4H-chromenes;RAPID COMMUN MASS SP;2001
3. Mass spectra of new substituted 2-amino-4H-pyrans: a retro-Diels-Alder reaction pattern;Rapid Communications in Mass Spectrometry;2000
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5. Reactions of 1,4-dihydropyridines (review);Chemistry of Heterocyclic Compounds;1993-05