565463-00-5

Upstream product

• 565462-98-8 tetrahydropyran-2-yl 6-O-triphenylmethyl-5-deoxy-5-thio-α-D-glucopyranoside 
• 453525-11-6 tetrahydropyran-2-yl 2,3,4,6-tetra-O-acetyl-5-deoxy-5-thio-α-D-glucopyranoside 
• 453524-96-4 tetrahydropyran-2-yl 5-deoxy-5-thio-α-D-glucopyranoside 
• 2746-25-0 p-Methoxybenzyl bromide 
• 565462-86-4 tetrahydropyran-2-yl 2,3,4-[tris-O-(4-methoxyphenyl)methyl]-6-O-triphenylmethyl-5-deoxy-5-thio-α-D-glucopyranoside 
• 137886-82-9 2,3,4,6-Tetra-O-acetyl-5-thio-α-D-glucopyranose 
• 76-83-5 trityl chloride 

Downstream Products

• 565462-89-7 methyl 6-[2',3',4'-tris-O-(4-methoxyphenyl)methyl-6'-O-(triphenyl)methyl-5'-deoxy-5'-thio-α-D-glucopyranosyl]-2,3,4-tri-O-benzoyl-α-D-glucopyranoside 
• 565462-90-0 methyl 6-O-[2',3',4'-[tris-O-(4-methoxyphenyl)methyl]-5'-deoxy-5'-thio-α-D-glucopyranosyl]-2,3,4-tri-O-benzoyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthetic studies on oligosaccharides composed of 5-thioglucopyranose units

Glycosylation reactions of 5-thioglucopyranosyl trichloroacetimidates bearing ethereal protective groups at the 2-O-position 14-15, and 37 proceed smoothly to give α-glycosides stereoselectively by using a catalytic amount of silyl triflate. This methodol