Pure and Applied Chemistry · 2006 · 52 citations · 1 references
Natural SciencesChemistryCatalysisGreen ChemistryOrganic ChemistryCoordination ChemistryCross-coupling ReactionsHeterocycle SynthesisOrganic SynthesisAlkenyl Halide CouplingHydroxyl FunctionalizationHydroxyl Group ProtectionMild Reaction ConditionsSilane CouplingSiliconSilyl Protecting GroupsSilylation Reactions
Abstract 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 K 2 CO 3 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.
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Metal-catalyzed cross-coupling reactions
Choice Reviews Online · 2005 · 320 citations