565462-97-7

Upstream product

• 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 
• 137886-82-9 2,3,4,6-Tetra-O-acetyl-5-thio-α-D-glucopyranose 
• 565462-95-5 tetrahydropyran-2-yl 2,3,4,6-[tetrakis-O-(4-methoxyphenyl)methyl]-5-deoxy-5-thio-α-D-glucopyranoside 

Downstream Products

• 565462-72-8 2,3,4,6-[tetrakis-O-(4-methoxyphenyl)methyl]-5-deoxy-5-thio-α-D-glucopyranosyl trichloroacetimidate 
• 565462-84-2 methyl 2,3,4-tri-O-benzoyl-6-O-[2',3',4',6'-[tetrakis-O-(4-methoxyphenyl)methyl]-5'-deoxy-5'-thio-α-D-glucopyranosyl]-α-D-glucopyranoside 
• 565462-83-1 methyl 2,3-di-O-benzoyl-6-O-(4-methoxyphenyl)methyl-4-O-[2',3',4',6'-[tetrakis-O-(4-methoxyphenyl)methyl]-5'-deoxy-5'-thio-α-D-glucopyranosyl]-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