Palladium-Catalyzed Regio- and Stereoselective Cross-Coupling of Baylis-Hillman Adducts and Bimetals: A Novel Method for the Synthesis of Substituted Allylsilanes and Allylgermanes
Cross-coupling reactions between Baylis-Hillman acetate adducts and bimetallic reagents (Si−Si, Ge−Ge) catalyzed by a phosphine-free palladium complex are described. 3-Substituted-2-carbonylallylsilanes and allylgermanes were isolated in high yields. The cross-coupling reactions are regio- and stere...
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Veröffentlicht in: | Organometallics 2005-02, Vol.24 (4), p.762-764 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Cross-coupling reactions between Baylis-Hillman acetate adducts and bimetallic reagents (Si−Si, Ge−Ge) catalyzed by a phosphine-free palladium complex are described. 3-Substituted-2-carbonylallylsilanes and allylgermanes were isolated in high yields. The cross-coupling reactions are regio- and stereoselective. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om0492451 |