Readily accessible and highly stable alkenyl- and aryl[2-(hydroxymethyl) phenyl]dimethylsilanes cross-couple with various aryl and alkenyl halides under mild reaction conditions employing K2CO3 as a base at 35-80 °C. The reaction tolerates a diverse range of functional groups including silyl protections. The silicon residue, cyclic silyl ether, is readily recovered and reused on a gram-scale synthesis. Intramolecular coordination of a proximal hydroxyl group is considered to efficiently form pentacoordinated silicates having a transferable group at an axial position. © 2006 IUPAC.
CITATION STYLE
Nakao, Y., Sahoo, A. K., Imanaka, H., Yada, A., & Hiyama, T. (2006). Alkenyl- and aryl[2-(hydroxymethyl)phenyl]dimethylsilanes: Tetraorganosilanes for the practical cross-coupling reaction. In Pure and Applied Chemistry (Vol. 78, pp. 435–440). https://doi.org/10.1351/pac200678020435
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