169237-18-7

Upstream product

• 142329-96-2 4-methoxybenzyl 4,6-O-benzylidene-β-D-glucopyranoside 
• 171412-20-7 (4-methoxybenzyl)-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 81381-72-8 (4-methoxyphenyl)methyl-β-D-glucopyranoside 
• 105-13-5 4-Methoxybenzyl alcohol 
• 142329-95-1 p-methoxybenzyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 108-24-7 acetic anhydride 
• 142329-98-4 4-methoxybenzyl O-<3,4,6-tri-O-benzoyl-2-(benzoyloxyimino)-2-deoxy-β-D-arabino-hexopyranosyl>-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 142329-97-3 4-methoxybenzyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 

Relevant academic research and scientific papers

A practical synthesis of mannosaminyl-β(1 → 4)-glucosyl-α(1 → 2)-rhamnose, the trisaccharide repeating unit of a Streptococcus pneumoniae capsular polysaccharide

An efficient chemical synthesis is described for the title trisaccharide repeating unit of the capsular polysaccharide of Streptococcus pneumoniae Type 19F. The key intermediate was a well-accessible indirect β-D-mannosaminyl donor, i.e. 2-(benzoyloxyimin

Expedient Synthesis of an Anomerically Modified Trisaccharide Component of the Capsular Polysaccharide From Streptococcus pneumoniae Type 19F

A practical stereoselective synthesis is described for α-D-ManNAc-(14)-α-D-(12)-L-Rha, an anomerically modified trisaccharide component of the capsular polysaccharide of Streptococcus pneumoniae type 19F.The key intermediary disaccharide, 2-(benzoyl