Methyl Trifluoropyruvate in Cyclocondensation Reactions with N-Substituted Ureas

Methyl Trifluoropyruvate in Cyclocondensation Reactions with N-Substituted Ureas

The transformations of methyl trifluoropyruvate in cyclocondensation reactions with N-substituted ureas, leading to 3-substituted 5-hydroxy- or 5-methoxy-5-trifluoromethylimidazolidine-2,4-diones, were studied. The possibility of using 5-hydroxy-3-(prop-2-in-1-yl)-5-trifluoromethylimidazolidine-2,4-...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Russian journal of general chemistry 2019, Vol.89 (1), p.153-156
Hauptverfasser: Sokolov, V. B., Aksinenko, A. Yu
Format: Artikel
Sprache:eng
Schlagworte:
Alkynes
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Cycloaddition
Diketones
Letters to the Editor
Phenothiazine
Substitutes
Ureas
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The transformations of methyl trifluoropyruvate in cyclocondensation reactions with N-substituted ureas, leading to 3-substituted 5-hydroxy- or 5-methoxy-5-trifluoromethylimidazolidine-2,4-diones, were studied. The possibility of using 5-hydroxy-3-(prop-2-in-1-yl)-5-trifluoromethylimidazolidine-2,4-dione for modifying phenothiazine with a copper-catalyzed alkyne-azide 1,3-dipolar cycloaddition was shown.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363219010286