Full Paper
Palladium-Catalyzed Cross-Coupling Reactions of Substituted Aryl(dimethyl)silanols
Article first published online: 16 DEC 2004
DOI: 10.1002/adsc.200404204
Copyright © 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Denmark, S. and Ober, M. (2004), Palladium-Catalyzed Cross-Coupling Reactions of Substituted Aryl(dimethyl)silanols. Advanced Synthesis & Catalysis, 346: 1703–1714. doi: 10.1002/adsc.200404204
Publication History
- Issue published online: 16 DEC 2004
- Article first published online: 16 DEC 2004
- Manuscript Accepted: 30 AUG 2004
- Manuscript Received: 28 JUN 2004
- Abstract
- References
- Cited By
Keywords:
- biaryls;
- C
C bond formation; - cesium carbonate;
- cesium hydroxide;
- fluoride-free;
- hydration effect
Abstract
Cesium carbonate and cesium hydroxide monohydrate are effective activators for the palladium-catalyzed cross-coupling of aryl(dimethyl)silanols with substituted aryl halides. Extensive optimization studies led to the identification of key variables (solvent, catalyst, additive, and hydration level) that influence the rate and selectivity of the process. Manipulation of these factors provides an effective coupling method of wide scope and generality. Electron-rich aryl(dimethyl)silanols undergo cross-coupling with aryl iodides and aryl bromides in high yields and high selectivity for the desired cross-coupling products. Alternatively, high yields of cross-coupling products could be obtained with electron-poor or ortho-substituted aryl(dimethyl)silanols when activated with cesium hydroxide monohydrate.

1615-4169/asset/2258_left.gif?v=1&s=480b85eb3acd0e8f47639c75e9ec7a59d53cd074)
1615-4169/asset/cover.gif?v=1&s=6b403eb4cdb02c56a05bd76afba87849efa73d61)