858129-86-9

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 114853-38-2 methyl 1-thio-β-L-fucopyranoside 

Downstream Products

• 858129-88-1 methyl 4-O-benzoyl-2-O-(4-methoxybenzyl)-1-thio-β-L-fucopyranoside 
• 858129-89-2 methyl 4-O-benzoyl-3-O-(tert-butyldimethylsilyl)-2-O-(4-methoxybenzyl)-1-thio-β-L-fucopyranoside 
• 858129-90-5 4-O-benzoyl-3-O-(tert-butyldimethylsilyl)-2-O-(4-methoxybenzyl)-α-L-fucopyranosyl bromide 
• 858129-92-7 methyl 4-O-benzoyl-3-O-(tert-butyldimethylsilyl)-2-O-(4-methoxybenzyl)-α-L-fucopyranosyl-(1->3)-4-O-benzoyl-2-O-(4-methoxybenzyl)-1-thio-β-L-fucopyranoside 

Relevant academic research and scientific papers

Synthesis of a (1→3)-linked α-L-fucose tetrasaccharide

Orthoester-protected benzyl and methyl 1-thiofucopyranosides could be opened to give fucopyranosides unblocked at position 3. Convergent glycosylations of such donors and acceptors led to the corresponding disaccharides, and their block condensation could