874906-01-1

Upstream product

• 88567-49-1 6-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranose 
• 88567-51-5 methyl [(2R,3R,4S,5R)-3,4,5-tribenzyloxy-6-oxo-tetrahydropyran-2-yl]acetate 
• 109-72-8 n-butyllithium 
• 874906-13-5 6-O-acetyl-2,3,4-tri-O-benzyl-1-C-n-butyl-α-D-glucopyranose 

Relevant academic research and scientific papers

Trifluoromethanesulfonic acid efficiently catalyzed the intramolecular glycosidation of 1-C-alkyl-D-hexopyranoses to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1]octane structures

The intramolecular glycosidation of the 1-C-alkyl-D-hexopyranose derivatives to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1] octane structures was investigated. We synthesized several 1-C-alkyl-2,3,4-tri- O-benzyl-D-hexopyranoses and found