152174-59-9

Upstream product

• 163523-19-1 3,4-Di-O-benzyl-6-O-tert-butyldiphenylsilyl-1,2-O-(methyl-orthoacetyl)-β-D-mannopyranose 
• 270087-60-0 3,4-di-O-benzyl-6-O-(tert-butyldimethylsilyl)-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 100-39-0 benzyl bromide 
• 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 

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 
• 674303-04-9 Acetic acid (2S,3S,4S,5R,6R)-6-[3-((2S,3S,4S,5R,6R)-3-acetoxy-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-ureidomethyl]-4,5-bis-benzyloxy-2-[3-(9H-fluoren-9-ylmethoxycarbonylamino)-propoxy]-tetrahydro-pyran-3-yl ester 
• 674302-98-8 Acetic acid (2S,3S,4S,5R,6R)-6-azidomethyl-4,5-bis-benzyloxy-2-[3-(9H-fluoren-9-ylmethoxycarbonylamino)-propoxy]-tetrahydro-pyran-3-yl ester 
• 674303-01-6 Acetic acid (2S,3S,4S,5R,6R)-6-aminomethyl-4,5-bis-benzyloxy-2-[3-(9H-fluoren-9-ylmethoxycarbonylamino)-propoxy]-tetrahydro-pyran-3-yl ester 
• 674302-99-9 [3-((2S,3S,4R,5R,6R)-6-Azidomethyl-4,5-bis-benzyloxy-3-hydroxy-tetrahydro-pyran-2-yloxy)-propyl]-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 674302-97-7 6-azdio-3,4-di-O-benzyl-6-deoxy-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 152157-69-2 6-O-allyl-3,4-di-O-benzyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 

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

Efficient Synthesis of Unsymmetrical Ureido-Linked Disaccharides

Five nonsymmetrical urea-linked disaccharides, in which two glycopyranoside units are bound at the 1→2, 1→4, and 1→6 positions, were efficiently synthesized. A mild and safe procedure, in which glycosyl isocyanates were coupled with a glycosylamine, was e

Building Units of Oligosaccharides, CIX. - Synthesis of Modified Oligosaccharides of N-Glycoproteins for Substrate Specificity Studies of N-Acetylglucosaminyltransferase I

A series of modified derivatives of the trisaccharide octyl α-D-Man(1-->3)-6)>-β-D-Man were synthesized for substrate specificity studies of N-acetylglucosaminyltransferase I (GlcNAc-T I).The hydroxyl groups at C-3, C-4 and C-6 of the α(1-->3

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