Methyl Trifluoropyruvate in Cyclocondensation Reactions with N-Substituted Ureas


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Аннотация

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.

Авторлар туралы

V. Sokolov

Institute of Physiologically Active Compounds of the Russian Academy of Sciences

Email: alaks@ipac.ac.ru
Ресей, Severnyi proezd 1, Chernogolovka, 142432

A. Aksinenko

Institute of Physiologically Active Compounds of the Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: alaks@ipac.ac.ru
Ресей, Severnyi proezd 1, Chernogolovka, 142432

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