38081-39-9

Upstream product

• 102219-47-6 2-O-benzoyl-3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 97133-48-7 1,2-O-Benzyliden-α-D-glucopyranose 
• 108-24-7 acetic anhydride 
• 4692-12-0 1,3,4,6-tetra-O-acetyl glucopyranose 
• 98-88-4 benzoyl chloride 
• 102219-46-5 1,3,4,6-tetra-O-acetyl-2-O-benzoyl-α-D-glucopyranoside 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 103664-30-8 3,4,6-tri-O-benzoyl-1,2-O-benzylidene-α-D-glucopyranose 

Relevant academic research and scientific papers

Practical synthesis of 1,2-O-benzylidene and 1,2-O-p-methoxybenzylidene hexopyranoses

An improved and practical synthesis of 1,2-O-benzylidene and 1,2-O-p-methoxybenzylidene hexopyranoses as useful synthons in carbohydrate chemistry is described. The reaction of 2-benzoyloxyglycosyl bromide with sodium borohydride using excess amount of po

Studies on Koenigs-Knorr Glycosidations

Mercury salt and silver triflate-promoted Koenigs-Knorr reactions of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide and 2-O-benzoyl-3,4,6-tri-O-acetyl-α-D-glucopyranosyl bromide with mono, di and trichloroethanol were studied.The products in each react