Dual Ligand-Enabled Nondirected C‒H Olefination of (Hetero)Arenes for the Synthesis of Clickable Derivatives

23 July 2025, Version 1
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

Herein, we present a highly efficient method for the late-stage introduction of ‘’clickable’’ alkyne moieties into different (hetero)arene scaffolds. A highly efficient dual ligand-based palladium catalyst combining an N-acylsulfonamide (NASA) ligand with an N-heterocycle enables the introduction of acrylate moiety bearing a terminal alkyne via nondirected C–H activation, providing a versatile platform for subsequent bioconjugation or activity-based protein profiling (ABPP) applications. The utility of the method is demonstrated through a broad substrate scope and the subsequent use of the obtained products in representative click reactions

Keywords

C-H Activation
Bioorthogonal Labelling
Palladium Catalysis
Click Reactions

Supplementary materials

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Supporting Information
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Experimental procedures, optimization of the reaction conditions, analytical data.
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