Journal of the Chinese Chemical Society · 2009 · 14 citations · 36 references
Natural SciencesChemical EngineeringChemistryCatalysisFunctional MaterialsInorganic ChemistryCatalyst DesignCatalyst PreparationCatalyst RegenerationCatalyst SynthesisCatalytic MaterialsSupported CatalystsChemoselective FunctionalizationChemoselective SynthesisRecyclable MaterialsSilane CouplingSilica Gel TreatmentSilica SupportsSilica Surface FunctionalizationSilylation Reactions
Abstract Silica‐supported tin chloride [SiO 2 ‐Sn(Cl) 4‐n ] has been prepared by mixing tin chloride with activated silica gel in toluene under refluxing conditions for one day. A range of primary, secondary, and tertiary alcohols as well as phenolic hydroxyl groups were converted into their corresponding trimethylsilyl ethers with hexamethyldisilazane in the presence of catalytic amounts of silica‐supported tin chloride at room temperature. An excellent chemoselective silylation of hydroxyl groups in the presence of other functional groups was also observed. This catalyst could be recycled and reused fifteen times without loss of efficiency.
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Greene's protective groups in organic synthesis
Choice Reviews Online · 2007 · 591 citations
George A. Olah, B. G. B. GUPTA, Subhash C. Narang et al. · The Journal of Organic Chemistry · 1979 · 118 citations