The Suzuki-Miyaura reaction is a widely used method for the formation of C-C bonds. It involves the coupling of an aryl or vinyl boronic acid (or boronate ester) with an aryl or vinyl halide or triflate in the presence of a palladium catalyst. The Pd-CS@SiO2 catalyst provides a suitable surface for this reaction, allowing the reactants to come into contact with the palladium center and facilitate the C-C bond formation.
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methyl (E)?3?(4?benzoylphenyl)acrylate
5-(4-methoxyphenyl)isoquinoline
[(C5H5)Fe(C5H3C(CH3)NC4H9)PdCl(P(C6H5)3)]
[2,6-(CH3)2C6H3-N=C(Ph)-C(Ph)(Me)-OH]PdCl2
