The axial chirality of carbodiimide was proposed in 1932, but the synthesis of carbodiimide with one-handed axial chirality has not been achieved because of the low barrier of racemization. This work presents a strategy to use a conformationally restrained cyclic structure for creating carbodiimides whose biases of the axial chirality (labeled as S NCN /R NCN ) are higher than 100:1, as determined by vibrational circular dichroism spectroscopy and density functional theory calculations.