130539-41-2

Upstream product

• 34339-69-0 2,4,6-tri-O-acetyl-3-O-benzyl-α-D-glucopyranosyl bromide 
• 107-18-6 allyl alcohol 
• 39686-94-7 3-O-benzyl-1,2,4,6-tetra-O-acetyl-D-glucopyranose 
• 108-24-7 acetic anhydride 
• 209911-52-4 allyl 3-O-benzyl-D-glucopyranoside 

Downstream Products

• 143419-05-0 N-[(2R,3R,4R,5S,6R)-4-((2S,3R,4S,5S,6S)-5-Azido-4-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-benzyloxymethoxymethyl-5-hydroxy-2-methoxy-tetrahydro-pyran-3-yl]-acetamide 
• 143419-04-9 N-[(2R,3R,4R,5S,6R)-4-((2S,3R,4S,5S,6S)-5-Azido-4-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-5-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl]-acetamide 
• 143419-13-0 Acetic acid (2R,3R,4R,5R,6R)-2-allyloxy-4-benzyloxy-6-benzyloxymethyl-5-trifluoromethanesulfonyloxy-tetrahydro-pyran-3-yl ester 
• 143419-12-9 Acetic acid (2R,3R,4R,5R,6R)-2-allyloxy-4-benzyloxy-6-benzyloxymethyl-5-methanesulfonyloxy-tetrahydro-pyran-3-yl ester 
• 143419-01-6 Acetic acid (2R,3R,4S,5S,6S)-2-allyloxy-5-azido-4-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-yl ester 
• 143419-02-7 Acetic acid (2R,3R,4S,5S,6S)-5-azido-4-benzyloxy-6-benzyloxymethyl-2-bromo-tetrahydro-pyran-3-yl ester 
• 143419-00-5 allyl 2-O-acetyl-3,6-di-O-benzyl-β-D-glucopyranoside 
• 143418-99-9 Acetic acid (2R,4aR,6R,7R,8S,8aR)-6-allyloxy-8-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 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 

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