653597-49-0

Upstream product

• 142924-31-0 S-ethyl 4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 653597-45-6 ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 653597-44-5 ethyl (β-D-xylopyranosyl)-(1->2)-3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 319922-00-4 ethyl 3-O-allyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 653597-46-7 ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-3-O-allyl-6-O-benzyl-1-thio-α-D-mannopyranoside 

Downstream Products

• 653597-58-1 2-azidoethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-(4,6-di-O-benzyl-α-D-mannopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 653597-57-0 2-azidoethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1->2)-(3-O-allyl-4,6-di-O-benzyl-α-D-mannopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of Cryptococcus neoformans Capsular Polysaccharide Structures. IV. Construction of Thioglycoside Donor Blocks and their Subsequent Assembly

Di- and trisaccharide thioglycoside building blocks, ethyl (2,3,4-tri-O-benzyl-β-D-xylopyranosyl)-(1 → 2)-3-O-allyl-4,6-di-O- benzyl-1-thio-α-D-mannopyranoside, ethyl (2,3,4-tri-O-benzyl-β-D- xylopyranosyl)-(1 → 2)-6-O-acetyl-3-O-allyl-4-O-benzyl-1-thio-α