198338-70-4

Upstream product

• 246162-56-1 methyl 6-O-allyl-3,5-di-O-benzyl-α-D-mannofuranoside 
• 246162-55-0 1,2-anhydro-6-O-allyl-3,5-di-O-benzyl-β-D-mannofuranose 
• 246162-57-2 methyl 6-O-allyl-2,3,5-tri-O-benzyl-α-D-mannofuranoside 

Relevant academic research and scientific papers

Glycosylation with 1,2-anhydromannofuranose benzyl ether as the glycosyl donor: A comparison between sugar pyranose and furanose acceptors for thelr primary hydroxy activity

Some 1→5 and 1→6 α-linked furano-disaccharide derivatives were synthesized using 1,2-anhydromannofiiranose as the glycosyl donor. Comparison of the glycosyl acceptors indicated that the activity of primary hydroxyl groups of glycofuranoses was much lower than that of glycopyranoses.

Detritylation of mono- and di-saccharide derivatives using ferric chloride hydrate

Quantitative detritylation of mono- and di-saccharide derivatives of diverse structure was achieved with FeCl3 · 6H2O in CH2Cl2 at room temperature. Benzyl, isopropylidene, isopropylthio, allyl, acetyl, and benzoyl O-protecting groups were not effected under the designated conditions.