Benzyl 2-Acetamido-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-4,6-benzylidene-α-D-glucopyranoside (CAS 196941-73-8)

Benzyl 2-Acetamido-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-4,6-benzylidene-α-D-glucopyranoside, a complex carbohydrate derivative, has garnered significant attention in carbohydrate chemistry research due to its unique structural features and versatile reactivity. This compound has been employed as a key building block in the synthesis of structurally diverse glycoconjugates, including glycopeptides, glycolipids, and glycosylated natural products. Its mechanism of action lies in its ability to act as a glycosyl donor in glycosylation reactions, facilitating the formation of glycosidic bonds between sugar residues. Researchers have exploited its distinctive glycosylation pattern to access complex carbohydrate architectures with tailored properties for various applications in chemical biology and materials science. Furthermore, Benzyl 2-Acetamido-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-4,6-benzylidene-α-D-glucopyranoside has been utilized as a tool to study carbohydrate-protein interactions and carbohydrate-mediated biological processes, offering insights into the roles of carbohydrates in cellular recognition events and signaling pathways. Its potential as a glycosyl donor in enzymatic glycosylation reactions has also been explored, highlighting its utility in the enzymatic synthesis of complex carbohydrates with high efficiency and selectivity. Overall, Benzyl 2-Acetamido-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-4,6-benzylidene-α-D-glucopyranoside serves as a valuable asset in carbohydrate chemistry research, enabling the synthesis of complex glycoconjugates and contributing to our understanding of carbohydrate biology and biochemistry.