Methyl 4,6-Di-O-acetyl-2,3-dideoxy-α-D-threo-hex-2-enopyranoside (CAS 6605-29-4)

Methyl 4,6-Di-O-acetyl-2,3-dideoxy-α-D-threo-hex-2-enopyranoside, a derivative of dideoxyhexose, plays a crucial role in carbohydrate chemistry and glycobiology research. Its unique structural features, including the acetyl groups and the unsaturated enopyranoside ring, confer distinctive reactivity and functionality suitable for diverse synthetic applications. In research, this compound has been utilized as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. Specifically, its functional groups enable selective derivatization and manipulation, facilitating the construction of structurally-defined carbohydrates for studies focused on carbohydrate-protein interactions, cell recognition processes, and biomaterials engineering. Moreover, its involvement in glycosylation reactions has been explored to explain the mechanisms and kinetics of glycosidic bond formation, providing insights into carbohydrate biosynthesis and glycoengineering strategies. Furthermore, the compound′s synthetic accessibility and versatility have contributed to its utility in the development of carbohydrate-based probes, sensors, and bioconjugates for various biotechnological and biomedical applications, demonstrating its significance as a valuable tool in glycobiology research.