Heteroatom‐directedCH borylation of cyclopropanes and cyclobutanes was achieved with silica‐supported monophosphane–Ir catalysts. Borylation occurred at the CH bonds located γ to the directingN or O atoms with exceptional cis stereoselectivity relative to the directinggroups. This protocol was applied to the borylation of a tertiary CH bond of a ring‐fused cyclopropane.