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.

Authors
Aleti R.R. 1 , Festa A.A. 1 , Voskressensky L.G. 1 , Van Der Eycken E.V.
Journal
Publisher
MDPI AG
Number of issue
18
Language
English
Status
Published
Number
5560
Volume
26
Year
2021
Organizations
  • 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
Keywords
2-phenyl benzamides; Arynes; Benzanilides; C-C and C-N bond activation; C-H bond activation; Carbonylation; Ketoximes and aldoximes; N-methoxy benzamides; Oxidation
Date of creation
16.12.2021
Date of change
16.12.2021
Short link
https://repository.rudn.ru/en/records/article/record/76657/
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