Beilstein Arch. 2025, 202545. https://doi.org/10.3762/bxiv.2025.45.v1
Published 07 Jul 2025
Azobenzenes are photoresponsive compounds widely used in molecular switches, light-controlled materials, and sensors, but despite extensive studies on symmetric derivatives, efficient methods for synthesizing non-symmetric analogues remain scarce due to regioselectivity issues, multi-step procedures, and limited applicability to tetra-ortho-substituted structures. Herein, we describe a direct, one-pot Pd-catalyzed dehydrogenative C–N coupling between aryl bromides and aryl hydrazines to access non-symmetric azobenzenes. The use of bulky phosphine ligands and sterically tuned substrates promotes selective N-arylation at the terminal nitrogen. The protocol tolerates a wide range of functional groups and enables the synthesis of well-decorated azobenzenes, including tetra-ortho-substituted derivatives. Notably, the reaction proceeds under an O2 atmosphere and in the presence of water, highlighting its robustness.
Keywords: Azo Compounds; Palladium; Cross-Coupling; Phosphine ligands; Domino catalysis
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Geminiani, L.; Junge, K.; Beller, M.; Soulé, J.-F. Beilstein Arch. 2025, 202545. doi:10.3762/bxiv.2025.45.v1
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