Issue 4, 2022

Synthesis of acridinones via palladium-catalyzed reductive annulation of 2-nitrobenzaldehydes and resorcinols

Abstract

The catalytic conversion of biomass-derived feedstocks into functional molecules is of significance to synthetic organic chemistry. Herein, through a palladium-catalyzed reductive annulation reaction of resorcinols and 2-nitrobenzaldehydes, we present a new approach for the direct synthesis of acridinone derivatives, featuring operational simplicity, good substrate compatibility, and readily available feedstocks.

Graphical abstract: Synthesis of acridinones via palladium-catalyzed reductive annulation of 2-nitrobenzaldehydes and resorcinols

Supplementary files

Article information

Article type
Research Article
Submitted
11 Nov 2021
Accepted
22 Dec 2021
First published
23 Dec 2021

Org. Chem. Front., 2022,9, 953-958

Synthesis of acridinones via palladium-catalyzed reductive annulation of 2-nitrobenzaldehydes and resorcinols

R. Xie, W. Mao, H. Jia, G. Lu, J. Sun, H. Jiang, H. Zhao and M. Zhang, Org. Chem. Front., 2022, 9, 953 DOI: 10.1039/D1QO01693H

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