International Journal on Minority and Group Rights. Том 10. 2003. С. 203-220
Synthesis of functionalized tetrahydropyridones by the tandem Knoevenagel—Michael—intramolecular ammonolysis—alkylation reaction
The tandem Knoevenagel—Michael—intramolecular ammonolysis—alkylation reaction was used to synthesize functionalized tetrahydropyridones. The molecular and crystal structures of four pyridone derivatives were studied by X-ray diffraction. © 2021, Springer Science+Business Media LLC.
Авторы
Dyachenko I.V. 1 , Dyachenko V.D. 1 , Dorovatovskii P.V. 2 , Khrustalev V.N. 3, 4 , Nenajdenko V.G. 5
Номер выпуска
11
Язык
Английский
Страницы
2145-2155
Статус
Опубликовано
Ссылка
Том
70
Год
2021
Организации
- 1 Lugansk State Pedagogical University, 2 ul. Oboronnaya, Lugansk, 91011, Ukraine
- 2 National Research Center “Kurchatov Institute”, 1 ul. Akad. Kurchatova, Moscow, 123182, Russian Federation
- 3 Peoples’ Friendship University of Russia (RUDN University), 6 ul. Miklukho-Maklaya, Moscow, 117198, Russian Federation
- 4 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., Moscow, 119991, Russian Federation
- 5 Lomonosov Moscow State University, 1 Leninskie Gory, Moscow, 119991, Russian Federation
Ключевые слова
alkylation; functionalized tetrahydropyridones; intramolecular ammonolysis; Knoevenagel reaction; Michael reaction; X-ray diffraction
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ПРОБЛЕМЫ СОЦИАЛЬНОЙ ГИГИЕНЫ, ЗДРАВООХРАНЕНИЯ И ИСТОРИИ МЕДИЦИНЫ. Том 29. 2021. С. 1470-1474