Regio-selective synthesis of polyazacyclophanes incorporating a pendant group as potential cleaving agents of mRNA 5′-cap structure

Abstract A terpyridine or an imidazole unit has been tethered to an N -protected polyazacyclophane to give the appropriate N -monofunctionalized polyazacyclophane. After mild deprotection, four polyazacyclophanes incorporating a pendant group were obtained in satisfactory yields. Their preliminary cleavage ability of mRNA 5′- cap model was studied at pH 7.2.