1,3,4,6-Tetra-O-acetyl-2-(α-L-fucopyranosyl)-α-D-galactopyranose (CAS 56822-34-5)

1,3,4,6-Tetra-O-acetyl-2-(α-L-fucopyranosyl)-α-D-galactopyranose, a complex carbohydrate derivative, has garnered considerable attention in biochemical and glycobiology research for its role as a versatile building block in the synthesis of oligosaccharides and glycoconjugates. This chemical compound serves as a critical intermediate in the enzymatic and chemical synthesis of structurally diverse fucosylated glycans, which are essential components of glycoproteins and glycolipids involved in various biological processes, including cell-cell recognition, signaling, and immune responses. Researchers exploit its chemical reactivity and selective functional group protection strategy to enable the regio- and stereo-controlled installation of fucose residues onto specific positions of oligosaccharide scaffolds, facilitating the creation of complex carbohydrate structures with tailored properties and functions. Furthermore, 1,3,4,6-Tetra-O-acetyl-2-(α-L-fucopyranosyl)-α-D-galactopyranose derivatives have found applications in the development of glycomimetics and carbohydrate-based probes for studying carbohydrate-protein interactions, cell surface recognition events, and glycobiological processes. Through its pivotal role in carbohydrate chemistry and glycoscience research, this compound continues to contribute to advancements in understanding the structure-function relationships of carbohydrates and their implications in biological systems.