Catalytic fluorination of unactivated C(sp(3))-H bonds

Organofluorine compounds have found widespread applications in the pharmaceutical and agrochemical industries. Efficient construction of organofluorine molecules is highly desirable. Catalytic transformation of C(sp(3))-H bonds into C(sp(3))-F bonds provides the simplest and most straightforward way to organofluorine compounds. This Highlight discusses the most recent findings in the field.