Benzyl N-Acetyl-4,6-O-benzylidene Normuranic Acid (CAS 14595-22-3)

Benzyl N-Acetyl-4,6-O-benzylidene Normuranic Acid is a pivotal compound in carbohydrate chemistry research, particularly in the synthesis of structurally diverse oligosaccharides and glycoconjugates. The chemical′s mechanism of action involves its utilization as a protected sugar derivative, where the benzylidene and acetyl groups serve as protecting groups for the hydroxyl functionalities, enabling selective glycosylation reactions. This protecting strategy ensures regioselectivity and stereochemistry control during glycosylation, facilitating the synthesis of complex carbohydrate structures. Researchers employ Benzyl N-Acetyl-4,6-O-benzylidene Normuranic Acid as a key building block in the construction of glycopeptides, glycolipids, and glycosylated natural products for various research applications. Its compatibility with diverse glycosylation methodologies allows for the creation of tailored carbohydrate derivatives with specific functional groups, enabling investigations into carbohydrate-protein interactions, carbohydrate-mediated signaling pathways, and carbohydrate-based materials. Additionally, this compound serves as a valuable tool in the development of carbohydrate-based probes, mimetics, and inhibitors for probing glycobiology and exploring carbohydrate-related diseases. Overall, Benzyl N-Acetyl-4,6-O-benzylidene Normuranic Acid plays a crucial role in advancing our understanding of carbohydrate chemistry and its implications in biological systems.