819798-34-0

Upstream product

• 100-39-0 benzyl bromide 
• 819798-33-9 phenyl 2-O-benzyl-3,4-O-benzylidene-1-thio-β-L-fucopyranoside 

Downstream Products

• 848416-63-7 phenyl 2,3-di-O-benzyl-4-O-(2-naphthyl)methyl-1-thio-β-L-fucopyranoside 
• 819798-37-3 phenyl 2,3-di-O-benzyl-4-O-succinoyl-1-thio-β-L-fucopyranoside 
• 848416-71-7 methyl 2,3-di-O-benzyl-4-O-(2-naphthyl)methyl-α-L-fucopyranosyl-(1->2)-3,4,6-tri-O-benzyl-β-D-galactopyranoside 

Relevant academic research and scientific papers

METHOD OF SYNTHESIZING SUGAR CHAIN

An object of the present invention is to provide a method for efficiently chemically synthesizing biomolecules including a nucleotide (nucleic acid), a peptide (protein), or a sugar chain, as representative examples. The present invention provides a metho

Synthesis of fully protected α-l-fucopyranosyl-(1→2)-β-d- galactopyranosides with a single free hydroxy group at position 2′, 3′ or 4′ using O-(2-naphthyl)methyl (NAP) ether as a temporary protecting group

Perbenzylated methyl α-l-fucopyranosyl-(1→2)-β-d- galactopyranosides having a single free OH group at position C-2′, C-3′ or C-4′ have been synthesized. Methyl 3,4,6-tri-O-benzyl- β-d-galactopyranoside was glycosylated either with phenyl 3,4-di-O-benzyl-2