Dual Ligand‐Enabled Nondirected C─H Olefination of (Hetero)Arenes for the Synthesis of Clickable Derivatives
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.
Authors
- Maria Hergert
- Manuel van Gemmeren (ORCID: https://orcid.org/0000-0003-3080-3579)
- Tommaso Braga
Institutions
- Christian-Albrechts-Universität zu Kiel (DE)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2026-02-05
- DOI
- https://doi.org/10.1002/chem.202600018
- Primary Topic
- Click Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- European Commission