145454-73-5

Upstream product

• 130539-41-2 allyl 2,4,6-tri-O-acetyl-3-O-benzyl-α-D-glucopyranoside 
• 39686-94-7 3-O-benzyl-1,2,4,6-tetra-O-acetyl-D-glucopyranose 
• 107-18-6 allyl alcohol 

Downstream Products

• 150969-26-9 allyl 3-O-benzyl-4,6-O-isopropylidene-β-D-glucopyranoside 
• 150969-33-8 allyl 2-O-acetyl-3-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-6-O-trityl-β-D-glucopyranoside 
• 150969-35-0 methyl uronate 
• 150969-34-9 allyl 2-O-acetyl-3-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-β-D-glucopyranoside 
• 150969-36-1 allyl 3-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-β-D-glucopyranosiduronic acid 
• 150969-28-1 allyl 2-O-acetyl-3-O-benzyl-6-O-trityl-β-D-glucopyranoside 
• 150969-27-0 Acetic acid (4aR,6R,7R,8S,8aR)-6-allyloxy-8-benzyloxy-2,2-dimethyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 143419-08-3 allyl 2-O-acetyl-3-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Strong aphicidal activity of GlcNAc(β1→4)Glc disaccharides: Synthesis, physiological effects, and chitinase inhibition

The synthesis of four GlcNAc(β1→4)Glc disaccharides containing 2-O-acetyl and/or 6-sulfate groups was performed in high yields with total 1,2-trans stereoselectivity. These disaccharides were evaluated as candidates for insect chitinase inhibition and aph

Synthesis of structural elements of the capsular polysaccharide of Streptococcus pneumoniae type 8

The synthesis is reported of propyl 4-O-α-D-galactopyranosyl-β-D-glucopyranosiduronic acid (25), 4-O-[4-O-(β-D-glucopyranosyluronic acid)-β-D-glucopyranosyl]-D-glucopyranose (34) and 4-O-(4-O-β-D-glucopyranosyl-α-D-glucopyranosyl)-D-galactopyranose (38),