81025-64-1

Upstream product

• 20379-60-6 α-D-Glucopyranosyl azide 
• 20379-61-7 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl azide 
• 4627-41-2 octa-O-acetyl-β-gentobiose 
• 81129-75-1 2,3,4,2',3',4',6'-hepta-O-acetyl-α-D-isomaltosyl bromide 
• 80977-08-8 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-acel-β-D-glucopyranosyl)-(1<*>6)-(2,3,4-tri-O-acetyl-N-)O-ethyl-N-(O-ethyl-N-benzyloxycarbonyl-L-β-aspartyl)-β-D-glucopyranosylamine 
• 81025-65-2 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-1,2,3,4-tetra-O-acetyl-β-D-glucopyranose 
• 80977-07-7 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-acetyl-β-D-glucopyranosylamine 
• 80977-04-4 O-(α-D-glucopyranosyl)-(1<*>6)-O-1,2,3,4-tetra-O-cetyl-β-D-glucopyranose 
• 80977-03-3 2,3,4-tri-O-acetyl-6-O-trityl-α-D-glucopyranosyl azide 
• 80977-05-5 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-acetyl-α-D-glucopyranosyl acide 
• 77437-54-8 1-azido-2,3,4-tri-O-acetyl-α-D-glucopyranose 
• 80977-09-9 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-acetyl-N-(O-ethyl-L-β-aspartyl)-β-D-glucopyranosylamine 
• 80977-08-8 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-acetyl-N-(O-ethyl-N-benzyloxycarbonyl-L-β-aspartyl)-α-D-glucopyranosylamine 
• 80977-06-6 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-acetyl-α-D-glucopyranosylamine 

Relevant academic research and scientific papers

An Efficient and Stereocontrolled Synthesis of the Nephritogenoside Core Structure

An efficient and stereocontrolled synthesis of the core trisaccharide 2 of nephritogenic glycopeptide, nephritogenoside 1 is described.Key to our synthetic strategy was β-selective glycosylation without neighboring group participation. Key words: nephrito

Application of n-pentenyl glycosides in the regio- and stereo-controlled synthesis of α-linked N-glycopeptides

The N-glycopeptides α-Glc-(1→Asn and α-Glc-(1→6)-β-Glc-(1→6)-α-Glc-(1→Asn have been synthesized efficiently from pent-4-enyl D-glucopyranoside derivatives. The methodology illustrates (a) a novel route for formation of the N-α-D-glucosyl-asparagine link,

Synthetic Studies on Nephritogenic Glycosides. Synthesis of α-Glc-(1->6)-β-Glc-(1->6)-α-Glc-(1->Asn)

Glucotriosyl asparagine 2, a proposed structure for the glycan part of nephritogenic glucopeptide 1 isolated from the glomerular basement-membrane of rat, was synthesized in regio- and stereo-selective manners starting from α-D-glycopyranosyl azide 8.The key intermediate for this synthesis was designed to be glucotriosyl azide 21, based on retrosynthetic considerations.