Onium amides, generated in situ from the combination of aminosilanes and onium fluorides (R(4)PF, R(4)NF), are employed for the first time as bases for catalytic deprotonative functionalization of C(sp(2))-H and activated C(sp(3))-H bonds under mild conditions.
由
氨基
硅烷和
氟化鎓(R(4)PF,R(4)NF)的组合就地生成的鎓酰胺首次用作C(sp(2))-H催化去质子功能化的基础和活化的C(sp(3))-H键在温和的条件下。