The thesis investigates the synthesis of the starting β-keto ester derived from Boc-protected glycine and its subsequent functionalization through alkylation and Michael addition. The use of various organocatalysts, including chiral squaramide catalysts, resulted in high enantioselectivity, enabling the formation of enantiomerically enriched products. The study employed analytical techniques such as NMR, IR, and HPLC to determine the structure and purity of the synthesized compounds. The results highlight the potential of the applied catalysts for the synthesis of complex molecules.
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