Journal of the American Chemical Society · 2004 · 54 citations · 26 references
Natural SciencesChemistryCatalysisGreen ChemistryOrganic ChemistryCatalyst DesignCatalytic MaterialsCross-coupling ReactionsNanocatalysisNanoparticle DesignSurface Functionalization Of NanomaterialsCatalytic SynthesisMild Reaction ConditionsPalladium CatalystsPalladium-catalyzed Cross-couplingSilane CouplingSilane FunctionalizationStereochemistry Of Sugar Derivatives
Palladium nanoparticles generated in situ from N,N-dimethyl-acetamide (DMA) solutions of PdX(2) (X = Cl(-), OAc(-), OCOCF(3)(-)) or Pd(2)(dba)(3) by reduction with alkyl silanes R(3)SiH (R = Me, Et, i-Pr, t-Bu) are selective catalysts for the cross-coupling of the silanes R(3)SiH with phenyl and vinyl thioethers forming the corresponding thiosilanes and silthianes in high yields and under mild conditions. The method is applicable to phenyl thioglycosides, giving access to thiosilyl glycosides a new class of sugar derivatives.
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