As part of this thesis, conjugates of ferrocene and cellobiose were prepared, aimed at studying the potential transfer of chirality from the sugar part of the molecule to the ferrocene core through supramolecular interactions. The inspiration for the synthesis of these compounds came from the class of ferrocene peptides, which possess the property of helical chirality, originating from the stabilization of conformers through intramolecular hydrogen bonds. Ferrocene peptides have found applications in the design of stereoselective catalysts and supramolecular systems, but their analogs containing saccharide units instead of amino acids have not yet been explored. The synthesis began with cellobiose octaacetate to which an alkyl linker was added by the method of direct glycosylation with bromoethanol. The bromide was then substituted with azide, which was reduced to an amino group. Under standard conditions for the preparation of amide bonds, the amino group was condensed with the carboxyl group of ferrocene(bis)carboxylic acid, yielding protected final compounds as products, from which acetate protective groups were removed in the final synthetic step. The final products and intermediates of the synthesis were characterized by spectroscopic techniques (NMR, IR).