2,3,5-trimethyl-pyridine; trimethylsilyl trifluoromethanesulfonate in tetrachloromethane T=25°C;

trimethylsilyl trifluoromethanesulfonate in tetrachloromethane T=20°C; reactions with mono- and bis-silylated reagent under var conditions; Product distribution;

trimethylsilyl trifluoromethanesulfonate in tetrachloromethane T=25°C; Yield given. Yields of byproduct given;

1: in dichloromethane T=-20°C; Sakurai Allylation; 0.0833333 h; Inert atmosphere; 2: With trimethylsilyl trifluoromethanesulfonate in dichloromethane T=-20°C; Sakurai Allylation; 4 h; Inert atmosphere;

trimethylsilyl trifluoromethanesulfonate in tetrachloromethane T=25°C; Yield given. Yields of byproduct given;