Juhász, LászlóBagaskara, Reyhan Kemal2026-01-082026-01-082025-11-25https://hdl.handle.net/2437/401828The aim of this research was to develop a method for synthesizing 1,2-thiodisaccharide-type galectin inhibitors with a C-galactopyranosyl-heterocyclic unit. To achieve this, a cyanogalactal was used as a key intermediate which was synthesized from D-galactose in a three-step reaction. The cyanogalactal underwent an elimination reaction to obtain the galactal derivative. The derivative was then reacted with different thiols to give the desired galactal–benzothiazole hybrid.29enGalectin inhibitorCarbohydrate-heterocycle hybridThiol-ene additionExperiments for the synthesis of carbohydrate-heterocycles hybrid molecule with potential galectin inhibitor activityChemistry::Organic ChemistyHozzáférhető a 2022 decemberi felsőoktatási törvénymódosítás értelmében.