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We report here an improved catalyst for the functionalization of Michael acceptors, involving CC bond formation via CH bond activation, using an in situ generated ruthenium active species. Moreover, on some particular substrates, the CH functionalization resulted unexpectedly in the formation of allylsilanes rather than in the expected conjugated adducts, affording a new straightforward methodology to access useful stereodefined trisubstituted allylsilanes via CH bond activation. Preliminary results have shown that they were reactive in the allylation of aldehydes, providing an access to alcohols bearing a quaternary carbon center.