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Chiral surfaces are an object of interest due to their application in catalysis, separation and sensors. Such surfaces can exhibit chirality on the molecular or supramolecular level. Previously, we have studied the thermodynamic features of adsorption on non-porous surfaces with supramolecular chirality. However, for their application in enantiomer separation, enantioselectivity and capacity should be greater. Porous adsorbents are promising for this purpose. In this work, the enantioselectivity of copper borophosphate LiCu2[BP2O8(OH)2] was studied. This zeotype material was obtained by hydrothermal synthesis without any source of chirality. Supramolecular chirality was achieved by spontaneous symmetry breaking via Viedma ripening. XRD and SEM were used to prove the synthesis accuracy. Enantioselectivity during adsorption was studied using the adsorption isotherms of α-pinene and limonene enantiomer analysis. The experimental isotherms were approximated by Langmuir, Dubinin–Radushkevich, Freundlich and Fowler–Guggenheim equations. The t-test was used to prove the reliability of the differences in enantiomer adsorption. The isosteric heats of adsorption were calculated from the adsorption isotherms. The data obtained have shown the ability of the LiCu2[BP2O8(OH)2] surface to recognize both α-pinene and limonene enantiomers. The molecules of α-pinenes adsorbed without pores, with the maximum enantioselectivity coefficient of 1.23 at 80 °C. Limonene molecules adsorbed in pore volume as single molecules or 1D chains. This phenomenon was proved by analysis of isosteric heats. The enantioselectivity of copper borophosphate to limonenes and α-pinenes was similar. The ability of pores with supramolecular chirality (and without molecular chirality) to recognize enantiomers was discovered in this paper for the first time. [ABSTRACT FROM AUTHOR]