244286-78-0

Upstream product

• 3616-19-1 1,2,3,6,2',3',4',6'-octa-O-acetylmaltose 
• 27891-73-2 phenylthio 2,3,4,6-terta hydroxy-α-D-glucopyranosyl-(1→4)-2,3,6-triylhydroxy-β-D-glucopyranoside 
• 87470-75-5 phenyl 4-O-(4,6-O-benzylidene-α-D-glucopyranosyl)-1-thio-β-D-glucopyranoside 
• 5346-81-6 phenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-1-thio-β-D-glucopyranoside 
• 108-98-5 thiophenol 
• 244286-77-9 phenyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranosyl)-1-thio-β-D-glucopyranoside 

Downstream Products

• 244286-79-1 methyl 2,3,6,2',3',4'-hexa-O-benzyl-α-D-maltoside 
• 244286-73-5 phenyl 2,3,6-tri-O-benzyl-4-O-(2,3,4-tri-O-benzyl-6-deoxy-α-D-xylohex-5-enopyranosyl)-1-thio-β-D-glucopyranoside 
• 244286-80-4 methyl 2,3,6,2',3',4'-hexa-O-benzyl-6'-deoxy-6'-iodo-α-D-maltoside 
• 244286-71-3 methyl 2,3,6-tri-O-benzyl-4-O-(2,3,4-tri-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranosyl)-α-D-glucopyranoside 

Relevant academic research and scientific papers

DISAL glycosyl donors for the synthesis of a linear hexasaccharide under mild conditions.

[reaction: see text] The new class of glycosyl donors with a methyl 3,5-dinitrosalicylate (DISAL) anomeric leaving group has proved efficient for glycosylation under strictly neutral, mildly basic, or mildly acidic conditions. Here, we report the synthesi

Direct synthesis of pseudo-disaccharides by rearrangement of unsaturated disaccharides

The series of unsaturated disaccharides 10-14 undergo stereoselective reductive rearrangement with TIBAL (triisobutylaluminium) to afford (1→4) and (1→6) ether-linked pseudo-disaccharides 2-9.