Zinc triflate-mediated nucleophilic addition of allytrimethylsilane, silyl enol ethers and terminal acetylenes to cyclic N-acyliminium ions at room temperature in CH2Cl2 is described. The corresponding a-substituted heterocycles were obtained in moderate to good yields. The versatility of this reagent was demonstrated in the one-pot generation of the N-acyliminium ion and the zinc alkynylide species, followed by their coupling reaction to afford propargylic adducts in moderate yields.o TEXTO COMPLETO DESTE ARTIGO, ESTARÁ DISPONÍVEL À PARTIR DE AGOSTO DE 2015.1522972300