314038-22-7

Upstream product

• 41308-76-3 allyl α-D-mannopyranoside 
• 314038-14-7 allyl 2,4-di-O-benzoyl-3-O-tert-butyldimethylsilyl-6-O-triphenylmethyl-α-D-mannopyranoside 

Downstream Products

• 1117751-18-4 allyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->3)-[2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl]-(1->6)-2,4-di-O-benzoyl-α-D-mannopyranoside 
• 904690-08-0 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->3)-[2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->6)-]-2,4-di-O-benzoyl-α-D-mannopyranosyl trichloroacetimidate 
• 1117751-22-0 3-azidopropyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->3)-[2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl]-(1->6)-2,4-di-O-benzoyl-α-D-mannopyranoside 
• 1117751-24-2 C₅₁H₆₃NO₂₆ 
• 904690-07-9 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->3)-[2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl]-(1->6)-2,4-di-O-benzoyl-α-D-mannopyranose 

Relevant academic research and scientific papers

Highly efficient and practical synthesis of 3,6-branched oligosaccharides.

[reaction: see text] A one-pot formation of the 3- and 6-OH differentially protected sugar synthon was described. A mannopyranosyl pentasaccharide and a glucopyranosyl hexasaccharide were prepared employing this new finding.

Efficient and practical syntheses of three pentasaccharides core structures corresponding to N-glycans

Three branched pentasaccharide derivatives and one tetrasaccharide were synthesized efficiently. The advantages of this method include a one-pot facile synthesis of 3,6-differentially protected mannose building block and an efficient strategy for oligosac