62327-60-0

Upstream product

• 67-56-1 methanol 
• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 74-88-4 methyl iodide 
• 4551-15-9 phenylthiotrimethylsilane 
• 605-81-2 methyl 2,3,4,6-tetra-O-methyl-α-D-glucopyranoside 
• 1139-97-5 2,3,4,6-tetra-O-methyl-D-glucopyranose 
• 882-33-7 diphenyldisulfane 
• 13992-16-0 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate 

Downstream Products

• 330476-89-6 phenyl 3,4,6-tri-O-methyl-β-D-glucopyranosyl sulfoxide 
• 3149-65-3 methyl 2,3,4,6-tetra-O-methyl-β-D-glucopyranoside 
• 605-81-2 methyl 2,3,4,6-tetra-O-methyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Facile Diastereoseparation of Glycosyl Sulfoxides by Chiral Stationary Phase

Separation of the diastereomers of glycosyl sulfoxides differing in the sulfur chirality has been difficult. This article presents a fast and scalable method for their diastereoseparation using a chiral stationary phase. The usefulness of this method was

Synthesis of pyranoid and furanoid glycals from glycosyl sulfoxides by treatment with organolithium reagents

Glycosyl sulfoxides can be conveniently transformed into pyranoid or furanoid glycals by treatment with organolithium reagents. The more likely reaction pathway involves a sulfoxide/metal exchange reaction to generate a glycosyllithium derivative that und

PHOTOINDUCED GENERATION OF GLYCOSYL CATIONS FROM THIOGLYCOSIDES

Photochemically induced cleavage of thioaryl β-D-glucopyranosides using 1,4-dicyanonaphthalene as an electron-transfer agent, produces glycosyl cations potentially useful in glycosylation reactions.