124595-23-9

Upstream product

• 37074-90-1 1,2,3,4-tetra-O-acetyl-6-O-trityl-β-D-glucopyranose 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 108-98-5 thiophenol 
• 83-87-4 D-glucose pentaacetate 
• 108-24-7 acetic anhydride 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 13992-16-0 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 13100-46-4 1,2,3,4-tetra-O-acetyl-β-D-glucopyranose 

Downstream Products

• 1610609-89-6 p-methoxyphenyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside 
• 1610609-85-2 p-methoxyphenyl 2,3,4-tri-O-acetyl-6-O-tert-butyldimethylsilyl-β-D-glucopyranosyl-(1→6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside 
• 124595-24-0 phenyl 2,3,4-tri-O-acetyl-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis, biological evaluation and structure-activity relationship studies of hederacolchiside E and its derivatives as potential anti-Alzheimer agents

Inspired by the previously reported neuroprotective activity of hederacolchiside E (1), we synthesized hederacolchiside E for the first time along with eleven of its derivatives. The neuroprotective effects of these compounds were further evaluated agains

Access to Galectin-3 Inhibitors from Chemoenzymatic Synthons

Chemoenzymatic strategies are useful for providing both regio- and stereoselective access to bioactive oligosaccharides. We show herein that a glycosynthase mutant of a Thermus thermophilus α-glycosidase can react with unnatural glycosides such as 6-azido

FACILE SYNTHESIS OF SILYLATED THIOGLYCOSIDES

The one pot conversion of 1,2,4,6-tetra-O-acetyl-β-D-glucopyranose, 1, into phenyl 2,4,6-tri O-acetyl-3-O-trialkylsilyl-1-thio-β-D-glucopyranosides, 3, is described.The method is applicable to use with galactopyranosyl-, 2-deoxyglucopyranosyl-, and ribofuranosyl-starting materials.