Отправить статью по E-mail Methyl Trifluoropyruvate in Cyclocondensation Reactions with N-Substituted Ureas
- Авторы: Sokolov V.1, Aksinenko A.1
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Учреждения:
- Institute of Physiologically Active Compounds of the Russian Academy of Sciences
- Выпуск: Том 89, № 1 (2019)
- Страницы: 153-156
- Раздел: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/222727
- DOI: https://doi.org/10.1134/S1070363219010286
- ID: 222727
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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.
Об авторах
V. Sokolov
Institute of Physiologically Active Compounds of the Russian Academy of Sciences
Email: alaks@ipac.ac.ru
Россия, Severnyi proezd 1, Chernogolovka, 142432
A. Aksinenko
Institute of Physiologically Active Compounds of the Russian Academy of Sciences
Автор, ответственный за переписку.
Email: alaks@ipac.ac.ru
Россия, Severnyi proezd 1, Chernogolovka, 142432
