4.6 Article

Suzuki-Miyaura cross-couplings of arenediazonium tetrafluoroborate salts with arylboronic acids catalyzed by aluminium hydroxide-supported palladium nanoparticles

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 10, Issue 3, Pages 495-497

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ob06752d

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Suzuki-Miyaura cross-couplings of arenediazonium salts with arylboronic acids catalyzed by highly active aluminium hydroxide-supported palladium nanoparticles catalyst have been investigated for the first time. The reactions are performed at 25 degrees C in MeOH without any base and ligand to afford biaryls in good to excellent yields under non-anhydrous and non-degassed conditions.

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