82469-72-5

Upstream product

• 82469-67-8 1,5-anhydro-3,4,6-tri-O-benzoyl-D-fructose O-benzoyloxime 
• 82469-67-8 C₃₄H₂₇NO₉ 
• 75414-21-0 3,4,6-tri-O-benzoyl-1,5-anhydro-D-fructose E-oxime 
• 98-88-4 benzoyl chloride 
• 82569-81-1 1,5-anhydro-3,4,6-tri-O-benzoyl-D-fructose oxime 

Downstream Products

• 118088-73-6 methyl 3,4,6-tri-O-benzoyl-2-(benzoyloxyimino)-2-deoxy-β-D-arabinohexopyranosyde 
• 118088-80-5 3,4,6-tri-O-benzoyl-2-(benzoyloxyimino)-2-deoxy-α-D-arabino-hexopyranose 
• 118088-79-2 methyl 4-O-<3,4,6-tri-O-benzoyl-2-(benzoyloxyimino)-2-deoxy-β-D-arabino-hexopyranosyl>-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 141514-07-0 4-pentenyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-β-D-arabino-hexopyranoside 
• 1198604-64-6 isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside 
• 142329-99-5 4-methoxybenzyl O-(2-acetamido-3,4,6-tri-O-benzoyl-2-deoxy-β-D-mannopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 142330-01-6 C₅₆H₅₄ClNO₁₃ 
• 171412-27-4 4-O-(2-acetamido-3,4,6-tri-O-benzoyl-2-deoxy-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranose 
• 118088-74-7 methyl 2-acetamido-3,4,6-tri-O-benzoyl-β-D-mannopyranosyde 
• 118088-82-7 methyl 4-O-(2-acetamido-3,4,6-tri-O-benzoyl-2-deoxy-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 118088-77-0 6-O-<2-acetamido-3,4,6-tri-O-benzoyl-2-deoxy-β-D-mannopyranosyl>-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 118088-83-8 methyl 4-O-(2-acetamido-2-deoxy-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 32087-36-8 methyl 2-acetamido-2-deoxy-β-D-mannopyranoside 
• 172949-55-2 4-methoxybenzyl 2,3-O-isopropylidene-4-O-<3,4,6-tri-O-benzoyl-2-(benzoyloxyimino)-2-deoxy-β-D-arabino-hexopyranosyl>-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Radical-mediated bromination of carbohydrate derivatives: Searching for alternative reaction conditions without carbon tetrachloride

KBrO3-Na2S2O4 in CH2Cl2-H2O or PhCF3-H2O biphasic solvent systems was applied to the bromination of several monosaccharide derivatives having capto-datively

Sugar Enolones, XVIII. - Stereocontrolled Functionalization at Proanomeric Centres by Photobromination. - A Novel Efficient Access to Oxo- and Oximinoglycosyl Bromides

Suitably O-blocked monosaccharides carrying an electron acceptor group such as an oxo or oximino function next to a proanomeric centre, readily homolyze the corresponding push-pull-substituted C-H bond to give under photobromination conditions the respect