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Updated: Aug 30, 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 20, 2014
Palladium-catalyzed coupling of sp(2)-hybridized tellurides
Gilson Zeni1, Antonio L Braga, Hélio A Stefani
1Departamento de Química, UFSM, 97105-900 Santa Maria, RS, Brazil. gzeni@quimica.ufsm.br
Abstract:
Vinylic tellurides are of importance due to their useful behavior as synthons and intermediates. Recently, the use of these compounds in place of vinylic halides or triflates in the palladium-catalyzed cross-coupling reaction has emerged as a powerful tool in the preparation of conjugated enyne and enediyne. In this way, vinylic tellurides can behave as aryl or vinyl carbocation equivalents. This review focuses on methods that involve the use of vinylic tellurides in palladium-catalyzed cross coupling reaction.
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