89104-67-6

Upstream product

• 108-24-7 acetic anhydride 
• 77388-95-5 2,4,6-tri-O-benzyl-β-D-glucopyranose 
• 89068-02-0 allyl 3-O-allyl-β-D-glucopyranose 
• 350254-95-4 3-O-allyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 37111-85-6 2,4,6-tri-O-benzyl-D-glucopyranose 
• 37111-85-6 2,4,6-tri-O-benzyl-L-allose 

Downstream Products

• 89068-05-3 3-O-acetyl-2,4,6-tri-O-benzyl-α-D-glucopyranosyl chloride 
• 127873-80-7 3-O-acetyl-2,4,6-tri-O-benzyl-D-glycopyranose 
• 76543-11-8 1,3-anhydro-2,4,6-tri-O-benzyl-β-D-glucopyranose 
• 89068-06-4 Acetic acid (2R,3R,4S,5R,6R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((2S,3S,4S,5R,6R)-2,3,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-4-yl ester 
• 89068-07-5 Acetic acid (2R,3R,4S,5R,6S)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((2S,3S,4S,5R,6R)-2,3,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

Synthesis of helicobacter-pylorus O2 serotype O antigen oligosaccharide compound

The invention discloses discloses synthesis of a helicobacter-pylorus O2 serotype O antigen oligosaccharide compound, and belongs to the field of organic synthesis. According to the synthesis, helicobacter-pylorus O2 serotype O-antigen disaccharide to tet

Direct amino acid catalyzed asymmetric synthesis of polyketide sugars

Back to the future: In a biomimetic asymmetric synthesis of sugars (see scheme) sequential cross-aldol reactions of simple aldehydes were catalyzed by amino acids. Deoxysugars were obtained with excellent chemoselectivity and up to > 99% ee. This transfor