334934-29-1

Upstream product

• 334934-28-0 3-trifluoroacetamidopropyl 2-acetamido-4,6-O-benzylidene-3-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 334934-32-6 3-trifluoroacetamidopropyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 334934-31-5 Benzoic acid (2S,4aR,6S,7R,8S,8aS)-7-acetoxy-6-{(2R,3S,4R,5R,6R)-5-acetylamino-4-benzyloxy-2-benzyloxymethyl-6-[3-(2,2,2-trifluoro-acetylamino)-propoxy]-tetrahydro-pyran-3-yloxy}-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester 
• 334934-34-8 Benzoic acid (2S,4aR,6S,7R,8R,8aS)-6-{(2R,3S,4R,5R,6R)-5-acetylamino-4-benzyloxy-2-benzyloxymethyl-6-[3-(2,2,2-trifluoro-acetylamino)-propoxy]-tetrahydro-pyran-3-yloxy}-7-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester 
• 334934-23-5 3-trifluoroacetamidopropyl (2-O-acetyl-3-O-benzoyl-β-D-galactopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 334934-24-6 3-trifluoroacetamidopropyl (3-O-benzoyl-β-D-galactopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 334934-33-7 3-trifluoroacetamidopropyl (4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 334934-25-7 N-{3-[(2R,3R,4R,5S,6R)-3-Acetylamino-4-benzyloxy-6-benzyloxymethyl-5-((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-propyl}-2,2,2-trifluoro-acetamide 
• 432023-49-9 3-trifluoroacetamidopropyl O-(6-O-benzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 

Relevant academic research and scientific papers

The presence of water improves reductive openings of benzylidene acetals with trimethylaminoborane and aluminium chloride

The acidic reagent formed in situ from anhydrous AlCl3 and H2O in 3:1 ratio is much more efficient for the reductive openings of the cyclic benzylidene acetals with Me3N·BH3 in tetrahydrofurane than the AlClsub

Synthesis of Neu5Ac- and Neu5Gc-α-(2 → 6′)-lactosamine 3-aminopropyl glycosides

In order to prepare 3-aminopropyl glycosides of Neu5Ac-α-(2 → 6′)-lactosamine trisaccharide 1, and its N-glycolyl containing analogue Neu5Gc-α-(2 → 6′)-lactosamine 2, a series of lactosamine acceptors with two, three, and four free OH groups in the galact