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Updated: Aug 18, 2026
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)
Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 21, 2014
Extremely high activity catalysts for the Suzuki coupling of aryl chlorides: the importance of catalyst longevity
Robin B Bedford1, Samantha L Hazelwood, Michael E Limmert
1School of Chemistry, University of Exeter, Exeter, UK EX4 4QD. r.bedford@ex.ac.uk
Abstract:
The incorporation of a new pi-acidic, orthometallated phosphite ligand into a palladium pre-catalyst gives considerably enhanced catalyst longevity and thus extremely high activity in the Suzuki coupling of deactivated, activated and sterically hindered aryl chloride substrates.
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