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Method Development for Synthesis of the Allal-Derived 2-Amino Free Reducing Sugar Rachel Starr Wednesday, 4/20 2:00-2:50 pm Altschul 805 Synthesizing amino sugar libraries for practical applications is a challenge in organic synthesis. Amino sugars are biologically important molecules that differ from normal other sugars by an amino substitution. They drive essential biological functions in bacterial, plant, and mammalian cells. Modifying these sugars changes the properties of the molecules to which they are attached, an approach especially relevant in drug discovery. Glycodiversification is the synthesis of analogues of naturally occurring carbohydrates. By Through optimizing glycodiversification, libraries of amino sugars can be synthesized and tested on drug scaffolds for to optimize drug properties such as potency and toxicity. This thesis work focuses on amidoglycosylation, deprotection, and neoglycosylation reactions, toward the goal of glycodiversification.