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Updated: Feb 7, 2026

Design, Synthesis, and Photochemical Properties of Clickable Caged Compounds
Published on: October 15, 2019
Dual Ligand-Enabled Nondirected C─H Olefination of (Hetero)Arenes for the Synthesis of Clickable Derivatives
Tommaso Braga1, Maria Hergert1, Manuel van Gemmeren1
1Otto Diels-Institut für Organische Chemie, Christian-Albrechts-Universität zu Kiel, Kiel, Germany.
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.
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