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
Supplementary materials
Title
Supporting Information
Description
Experimental procedures, optimization of the reaction conditions, analytical data.
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