171865-45-5

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 113842-87-8 allyl α-D-glucopyranosyl-(1->4)-β-D-glcopyranoside 
• 97777-13-4 allyl O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-acetyl-β-D-gluco-pyranoside 

Downstream Products

• 171412-01-4 allyl O-(2,3-di-O-benzyl-6-O-trityl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 171411-89-5 allyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 113879-86-0 allyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 113842-89-0 allyl O-(2,3-di-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of Glucose-Containing Linear Oligosaccharides Having α(1->4) and α(1->6) Linkages Using Stereoselective Dehydrative Glycosylation

Glycogen-storage-disease-relating linear tetra-, hexa-, and octasaccharides of D-glucose having α(1->4) and α(1->6) linkages were synthesized using a stereoselective dehydrative glycosylation with a reagent mixture of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, N,N-dimethylacetamide, and triethylamine.A cross-condensation of a quasi-stoichiometric amount of a donor and an acceptor of an octasaccheride, followed by deprotection, afforded a glucohexadecasaccharide.