152157-69-2

Upstream product

• 29073-91-4 1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 79218-90-9 6-O-acetyl-3,4-di-O-benzyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 106-95-6 allyl bromide 
• 152174-59-9 3,4-di-O-benzyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranoside 

Downstream Products

• 152157-71-6 octyl 6-O-(2-O-acetyl-6-O-allyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 152157-64-7 octyl 6-O-(6-O-allyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 152157-70-5 Acetic acid (3S,4S,5R,6R)-6-allyloxymethyl-4,5-bis-benzyloxy-2-chloro-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Synthesis of a tristearoyl lipomannan via preactivation-based iterative one-pot glycosylation

A convergent and efficient strategy was developed for the synthesis of lipomannan (LM), useful for vaccine development. Thioglycosides were employed as glycosyl donors to construct two key pseudotrisaccharide and tetramannose intermediates through preacti

Building Units of Oligosaccharides, CX. - Synthesis of Potential Inhibitors of N-Acetylglucosaminyltransferase I

Modified derivatives of the trisaccharide octyl α-D-Man(1-->3)-6)>-β-D-Man were synthesized by attaching reactive groups via a pentyl spacer to the 4'-OH and 6'-OH group.Glycosylation steps were carried out by using the trichloroacetimidate m

Acceptor-substrate recognition by N-acetylglucosaminyltransferase-V: Critical role of the 4''-hydroxyl group in β-D-GlcpNAc-(1->2)-α-D-Manp(1->6)-β-D-Glcp-OR

The enzyme N-acetylglucosaminyltransferase-V (GlcNAcT-V) transfers GlcNAc from UDP-GlcNAc to the OH-6' group of oligosaccharides terminating in the sequence β-D-GlcpNAc-(1->2)-α-D-Manp-(1->6)-β-D-Glcp (or Manp)-OR (5, R = (CH2)7CH3) to yield the sequence