127570-64-3

Upstream product

• 4779-31-1 Z-Asp-OBn 
• 75-05-8 acetonitrile 
• 139299-89-1 phenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-glucopyranoside 
• 441310-81-2 pent-4-enyl 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-D-glucopyranoside 
• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 182074-52-8 pent-4-enyl α,β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 143436-69-5 phenyl 6-O-(tert-butyldiphenylsilyl)-1-thio-β-D-glucopyranoside 
• 441311-03-1 pent-4-enyl 6-O-tert-butyldiphenylsilyl-D-glucopyranoside 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 127594-29-0 2,3,4-tri-O-benzyl-N-(benzyl N-benzyloxycarbonyl-L-β-aspartyl)-6-O-tert-butyldiphenylsilyl-α-D-glucopyranosylamine 
• 127570-61-0 2,3,4-tri-O-benzyl-N-(benzyl N-benzyloxycarbonyl-L-β-aspartyl)-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,