191034-33-0

Upstream product

• 98-88-4 benzoyl chloride 
• 18464-08-9 2,3,6,2',3',4',6'-hepta-O-acetyl-lactose 
• 34957-73-8 methyl 9-hydroxynonanoate 
• 160720-83-2 (2,6-di-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-α/β-D-glucopyranosyl trichloroacetimidate 
• 196305-13-2 Acetic acid (2S,3R,4S,5R,6R)-3-acetoxy-6-acetoxymethyl-2-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-5-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 
• 196305-14-3 (2S,3R,4S,5R,6R)-2-{(2R,3S,4R,5R,6S)-6-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 
• 196305-18-7 Thexyldimethylsilyl (2,6-di-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-β-D-glucopyranoside 
• 160720-82-1 (2S,3R,4R,5S,6R)-2-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-5-((3aS,4R,6S,7R,7aR)-7-hydroxy-4-hydroxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yloxy)-6-hydroxymethyl-tetrahydro-pyran-3,4-diol 
• 75795-58-3 4-O-(3,4-O-isopropylidene-β-D-galactopyranosyl)-D-glucopyranose 

Downstream Products

• 432022-71-4 8-methoxycarbonyloctyl-4'-O-acetyl-2,3,6,2',6'-penta-O-benzoyl-β-D-lactoside 
• 160720-73-0 8-methoxycarbonyloctyl-2,3,6,2',6'-penta-O-benzoyl-β-D-lactoside 

Relevant academic research and scientific papers

Large-scale chemical and enzymatic synthesis of a Clostridium difficile toxin A binding trisaccharide

Trisaccharide 1, 8-methoxycarbonyloctyl-O-(α-D-galactopyranosyl) -(1-→3)-(β-D-galactopyranosyl)-(1-→4)-β-D-glucopyranoside, linked to a solid support can be used to remove Cloxtridium difficile toxin A from the intestinal tract. Therefore, multi-gram chem

A simple access to lactose-derived building blocks required in glycoconjugate synthesis

Lactose was readily transformed into thexyldimethylsilyl (3,4-O-isopropylidene-β-D-galactopyranosyl)-(1 → 4)-β-D-glucopyranoside (5); this compound served as intermediate for the generation of partially O-protected lactose building blocks required in olig

Efficient synthesis of lactoneo series antigens H, Lewis X (Lex), and Lewis Y (Ley)

Regioselective 61,6b-di-O-benzoylation of azidolactose 4 furnished derivative 6 which permitted ensuing regioselective 2b-O-fucosylation, 2b,3a-di-O-fucosylation, or regioselective 2b-O-benzoylation and then 3a-O-fucosylation, respectively, thus providing