Synthetic strategies in the preparation of phenanthridinones

Phenanthridinones are important heterocyclic frameworks present in a variety of complex natural products, pharmaceuticals and displaying wide range of pharmacological actions. Its structural importance has evoked a great deal of interest in the domains of organic synthesis and medicinal chemistry to develop new synthetic methodologies, as well as novel compounds of pharmaceutical interest. This review focuses on the synthesis of phenanthridinone scaffolds by employing arylaryl, N-aryl, and biaryl coupling reactions, decarboxylative amidations, and photocatalyzed reactions. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Авторы
Aleti R.R. 1 , Festa A.A. 1 , Voskressensky L.G. 1 , Van Der Eycken E.V.
Журнал
Издательство
MDPI AG
Номер выпуска
18
Язык
Английский
Статус
Опубликовано
Номер
5560
Том
26
Год
2021
Организации
  • 1 Organic Chemistry Department, Science Faculty, RUDN University, Miklukho-Maklaya st., 6, Moscow, 117198, Russian Federation
  • 2 Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, Leuven, B-3001, Belgium
Ключевые слова
2-phenyl benzamides; Arynes; Benzanilides; C-C and C-N bond activation; C-H bond activation; Carbonylation; Ketoximes and aldoximes; N-methoxy benzamides; Oxidation
Дата создания
16.12.2021
Дата изменения
16.12.2021
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/76657/
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