Dual strategy approach for an aliphatic nitrile directing group-assisted palladium-catalyzed meta-C–H arylation/acetoxylation of arenes

Abstract

The meta-selective arylation of simple aliphatic nitrile-bearing arylmethanesulfonic acid derivatives under microwave-accelerated conditions has been developed. Additionally, the meta-arylation of 3-phenylpropanoic acid esters tethered to a nitrile template was achieved under conventional heating conditions. Furthermore, the feasibility of meta-acetoxylation was tested. Moreover, the strategy was found to be suitable for achieving drug diversification.

Graphical abstract: Dual strategy approach for an aliphatic nitrile directing group-assisted palladium-catalyzed meta-C–H arylation/acetoxylation of arenes

Supplementary files

Article information

Article type
Communication
Submitted
12 Mar 2026
Accepted
08 Apr 2026
First published
09 Apr 2026

Org. Biomol. Chem., 2026, Advance Article

Dual strategy approach for an aliphatic nitrile directing group-assisted palladium-catalyzed meta-C–H arylation/acetoxylation of arenes

R. Kaustubh, D. Srinivas, S. Challapalli and G. Satyanarayana, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D6OB00415F

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