Issue 24, 2022

Pd/Cu catalyzed carbonylation of α-aminoaryl-tethered alkylidenecyclopropanes: synthesis of furoquinoline derivatives

Abstract

A Pd/Cu catalyzed carbonylation of α-aminoaryl-tethered ACPs for the synthesis of furoquinoline derivatives has been developed. Oxygen was used as the terminal oxidant in this reaction. A range of furoquinoline derivatives were efficiently prepared in good to excellent yields via the incorporation of a carbonyl group into the product with the cleavage of the proximal C–C bond of the ACPs.

Graphical abstract: Pd/Cu catalyzed carbonylation of α-aminoaryl-tethered alkylidenecyclopropanes: synthesis of furoquinoline derivatives

Supplementary files

Article information

Article type
Research Article
Submitted
08 Sep 2022
Accepted
20 Oct 2022
First published
21 Oct 2022

Org. Chem. Front., 2022,9, 6802-6807

Pd/Cu catalyzed carbonylation of α-aminoaryl-tethered alkylidenecyclopropanes: synthesis of furoquinoline derivatives

L. Li, H. Zeng, Y. Zhang, J. Liang, X. Zhang and J. Peng, Org. Chem. Front., 2022, 9, 6802 DOI: 10.1039/D2QO01420C

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