Palladium-catalyzed sequential three-component reactions to access vinylsilanes
Bo Zhou1, Ailan Lu1, Changdong Shao1
1School of Chemical Science and Engineering, Shanghai Key Laboratory of Chemical, Assessment and Sustainability, Tongji University, 1239 Siping Road, Shanghai, 200092, P. R. China. zhangyanghui@tongji.edu.cn.
Abstract:
A palladium-catalyzed sequential three-component reaction has been developed. The palladacycles, generated through cascade reactions of aryl halides and alkynes, are the key intermediates and react with hexamethyldisilane to form disilylated products. The reaction represents a useful preparative method for vinylsilanes, and the vinylsilanes can be transformed into tetrasubstituted alkenes.
More Related Videos
Related Concept Videos
Base-Catalyzed Aldol Addition Reaction
Acid-Catalyzed Aldol Addition Reaction
Components of Stress
Interestingly, the hidden cube faces also experience these stresses, equal and...
Components of Language
Acid-Catalyzed Ring-Opening of Epoxides
Base-Catalyzed Ring-Opening of Epoxides
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)

