2,3,4-Tri-O-benzoyl-α-D-glucuronic Acid Methyl Ester

2,3,4-Tri-O-benzoyl-α-D-glucuronic Acid Methyl Ester is a vital compound in carbohydrate chemistry research, primarily used for synthesizing complex oligosaccharides and glycoconjugates. Its mechanism of action involves the introduction of a trichloroacetimidate moiety at the anomeric position of the glucuronic acid residue, serving as an efficient glycosyl donor in glycosylation reactions. This enables the stereoselective assembly of glucuronic acid-containing oligosaccharides, facilitating the study of their biological functions and interactions. Researchers utilize this compound as a versatile building block for synthesizing glycans with tailored structures, essential for investigating carbohydrate-mediated processes like cell signaling, inflammation, and microbial recognition. Moreover, it finds applications in developing glycan-based materials such as glycoprotein mimetics and glycan microarrays for studying carbohydrate-protein interactions and glycan-binding events. Its strategic use in chemical synthesis provides valuable insights into the roles of glucuronic acid-containing glycans in various biological systems, offering potential avenues for designing novel glycomimetics and glycan-based tools for research in glycobiology, immunology, and biomaterials science.