The principal domain of our activity is the enantioselective synthesis of natural products using simple chiral auxiliaries of natural or synthetic origin. Isoquinoline and indole alkaloids, as well as pharmacologically important heterocycles have been often chosen as synthetic targets. We are interested in the development of new reagents or synthetic methods that allow highly selective asymmetric transformations with the use of various enantiopure substrates (amino acids, alkaloids, terpenes and carbohydrates).