34621-77-7

Upstream product

• 530-26-7 D-Mannose 
• 3459-18-5 4-nitrophenyl N-acetyl-β-D-glucosaminide 
• 14362-46-0 1,2,3,6-tetra-O-acetyl-4-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranosyl)-D-glucopyranose 
• 14362-46-0 4-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-mannopyranosyl)-1,2,3,4,6-tetra-O-acetyl-α,β-D-glucopyranose 
• 70056-64-3 3-O-Acetyl-1,6-anhydro-2-O-benzyl-β-D-galactopyranose 
• 76909-65-4 1,6-Anhydro-2-O-benzyl-3,4-O-(1-methoxyethyliden)-β-D-galactopyranose 
• 55287-63-3 1,6-anhydro-2-O-benzyl-β-D-galactopyranose 
• 76909-67-6 3-O-Acetyl-4-O-(6-O-acetyl-2-azido-3,4-di-O-benzyl-2-desoxy-α-D-glucopyranosyl)-1,6-anhydro-2-O-benzyl-β-D-galactopyranose 
• 76909-75-6 4-O-(2-Acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-glucopyranosyl)-1,3,6-tri-O-acetyl-2-O-benzyl-D-galactopyranose 
• 76909-73-4 4-O-(2-Acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-glucopyranosyl)-3-O-acetyl-1,6-anhydro-2-O-benzyl-β-D-galactopyranose 

Relevant academic research and scientific papers

Unusual nonreducing sugar GlcNAcβ(1 mutually implies 1)Manβ formation by β-N-acetylhexosaminidase from Aspergillus oryzae

β-N-Acetylhexosaminidase from Aspergillus oryzae catalyzes the transfer of N-acetylglucosamine moiety from pNP-β-GlcNAc to mannose giving major product GlcNAcβ(1 mutually implies 1)Manβ (1a), and GlcNAcβ(1 mutually implies 3)Manα/β (2a) and GlcNAcβ(1 mutually implies 6)Manα/β (3a) as two minor products.

SYNTHESE VON TRISACCHARID-EINHEITEN DER KAPSELPOLYSACCHARIDE VON Streptococcus pneumoniae

In the presence of silver silicate as promoter, the reaction of gycosyl bromides of 2-azido-2-deoxy-D-mannose with 1,6-anhydro-2,3-di-O-benzyl-β-D-glucopyranoside led to derivatives of the disaccharide β-D-ManpNAc-(1->4)-D-Glcp.The derivatives were activa

Chemical Modification of Maltose. VII. Synthesis of 4-O-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-D-glucopyranose (GlcNAcα1->4Glc)

1,6-Anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-β-maltose (5), a maltose derivative having only one unprotected hydroxyl group at the C-2' position, was synthesized from 1,6-anhydro-4',6'-O-benzylidene-2'-O-tosyl-β-maltose (2) by benzylation followed

Bausteine von Oligosacchariden, XXII. Synthese der Trisaccharid-Sequenz α-D-GlcNAc-(1-4)-β-D-Gal-(1-4)-D-GlcNAc aus blutgruppenaktiven Substanzen

A directly stereoselective α-glycoside synthesis to oligosaccharides succeeds in the presence of AgClO4/Ag2CO3 in methylene chloride with the α-bromide 1 of 2-azido-2-desoxy-D-glucose.By reaction with 1 the disaccharides 3, 7a, 7b, 18 and the trisaccharid