101696-00-8

Upstream product

• 1214-98-8 phenyl 1-thio-β-D-fucopyranoside 
• 77-76-9 2,2-dimethoxy-propane 
• 141193-62-6 Phenyl-2,3,4-tri-O-acetyl-6-desoxy-1-thio-β-D-galactopyranosid 

Downstream Products

• 257936-70-2 phenyl 6-deoxy-3,4-O-isopropylidene-2-O-pivaloyl-1-thio-β-D-galactopyranoside 
• 257936-51-9 phenyl 2-O-benzoyl-6-deoxy-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside 
• 257936-72-4 phenyl 6-deoxy-2,3-di-O-pivaloyl-1-thio-β-D-galactopyranoside 
• 257936-53-1 phenyl 2,3-di-O-benzoyl-6-deoxy-1-thio-β-D-galactopyranoside 
• 257936-74-6 phenyl 4-O-chloroacetyl-6-deoxy-2,3-di-O-pivaloyl-1-thio-β-D-galactopyranoside 
• 257936-58-6 phenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-1-thio-β-D-galactopyranoside 
• 257936-78-0 methyl O-(6-deoxy-2,3-di-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 257936-76-8 methyl O-(4-O-chloroacetyl-6-deoxy-2,3-di-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 257936-68-8 methyl O-(6-deoxy-2,3-di-O-pivaloyl-4-O-trifluoromethylsulfonyl-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 257936-60-0 methyl O-(2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Glycodiversification for the optimization of the kanamycin class aminoglycosides

In an effort to optimize the antibacterial activity of kanamycin class aminoglycoside antibiotics, we have accomplished the synthesis and antibacterial assay of new kanamycin B analogues. A rationale-based glycodiversification strategy was employed. The a

β-Acarbose. VIII the synthesis of some N-linked carba-oligosacchandes

Two carbohydrate triflates have been used to alkylate a 1-epivalienamine derivative to give small amounts of the desired secondary amines, in addition to amounts of the products of elimination. Deprotection of the secondary amines afforded a carba-disacch