173206-22-9

Upstream product

• 604-69-3 β-D-glucose pentaacetate 
• 10343-15-4 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-allyloxy-tetrahydro-pyran-4-yl ester 
• 2595-07-5 allyl β-D-glucopyranoside 
• 6207-44-9 1-allyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

An access to glycoconjugate libraries through multicomponent reactions

Four-component reactions: The Ugi reaction of four suitably functionalized carbohydrate derivatives (as a per-O-benzylated amine, an aldehyde, a carboxylic acid, and an isocyanide) allow the effective assembly of diverse compound libraries. The complex gl

Synthesis of a Symmetric Multivalent Molecule containing four Carbohydrate Substituents

Starting with allyl- and pent-4-enyl-β-D-glucopyranosides 4-7, different D-Glucose units (8-15) containing alkyl spacers of variable lenght and with different end groups can be prepared.Reaction of four equivalents of the caesium salt derived from propan-4-carboxyl-1-yl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 15 with pentaerythrityltetrabromide yields the tetravalent molecule 16. - Keywords: Carbohydrates; Dendrimers; Spacer.