In this diploma thesis, the synthesis of D-glucose mono- and bis-conjugates of ferrocene was carried out, and also an N-acetyl-D-glucosamine mono-conjugate of ferrocene. To ensure conformational flexibility and thus the formation of strong hydrogen bonds between the carbohydrate rings, an ethylene link was planned between ferrocene and the sugar parts of the molecule. In the case of monosubstituted derivatives, the induction of helical chirality of ferrocene is not possible, given that only one of its rings has a sugar unit attached, thus these derivatives serve only for comparison. It is expected that in disubstituted derivatives, with sugar units attached to the both rings of ferrocene, intramolecular hydrogen bonds will form, which should induce helical chirality of ferrocene due to the chirality of the sugar. The synthesis of D-glucose derivatives was carried via direct glycosylation of peracetylated D-glucose with 2-bromoethanol as a glycosidic bond acceptor, and in the case of the N-acetyl-D-glucosamine derivative, the synthesis was performed by glycosylation of the oxazoline intermediate with 2-bromometalnol. The resulting bromides were substituted with an azide, which was then reduced to the amine for the purpose of condensation with ferrocene (di)carboxylic acid. Product characterization was carried out using spectroscopic methods (IR, NMR).