124813-97-4

Upstream product

• 100-52-7 benzaldehyde 
• 124813-96-3 methyl 2,3,4-tri-O-benzyl-6-O-(2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-α-D-glucopyranoside 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 39686-94-7 1,2,4,6-tetra-O-acetyl-3-O-benzyl-β-D-glucopyranose 
• 97590-76-6 benzyl-O-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 124813-98-5 Imidazole-1-sulfonic acid (4aR,6R,7R,8S,8aR)-8-benzyloxy-2-phenyl-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 

Relevant academic research and scientific papers

PREPARATION OF OLIGOSACCHARIDES WITH β-D-MANNOPYRANOSYL AND 2-AZIDO-2-DEOXY-β-D-MANNOPYRANOSYL RESIDUES BY INVERSION AT C-2 AFTER COUPLING

Di- and tri-saccharides with a 2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl unit were prepared by coupling 1,2,4,6-tetra-O-acetyl-3-O-benzyl-β-D-glucopyranose (1) to suitably, partially benzylated, acceptor sugar derivatives.Deacetylation followed by acetalation gave 3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyl derivatives which were treated with N,N'-sulfuryldi-imidazole.The resulting 2-imidazylate group was displaced easily with inversion by benzoate or azide, leading to β-D-mannopyranosyl or 2-azido-2-deoxy-β-D-mannopyranosyl derivatives, respectively.Protected derivatives of β-D-Manp-(1->4)-D-Glc, β-D-Manp-(1->4)-D-Man,β-D-Manp-(1->4)-β-D-Manp-(1->4)-D-Glc, 2-azido-2-deoxy-β-D-Manp-(1->4)-D-Glc, and 2-azido-2-deoxy-β-D-Manp-(1->6)-D-Glc were prepared thus.