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
Журнал
Russian Chemical Bulletin
Номер выпуска
11
Язык
Английский
Страницы
2145-2155
Статус
Опубликовано
Ссылка
Внешняя ссылка
DOI
10.1007/S11172-021-3326-9
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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