36874-86-9

Upstream product

• 19879-84-6 tetraacetyl thioglucose 
• 540-37-4 p-aminoiodobenzene 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 1849-36-1 para-nitrobenzenethiol 
• 68667-01-6 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-((4-nitrophenyl)thio)tetrahydro-2H-pyran-3,4,5-triyl triacetate 

Downstream Products

• 62205-46-3 p-N-acetamidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 
• 1107660-52-5 p-azidophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

Small molecule glycoconjugates with anticancer activity

Glycoconjugates are combinations of sugar moieties with organic compounds. Due to their biological resemblance, such structures often have properties that are desirable for drugs. In this study we designed and synthesised several glycoconjugates from smal

Palladium-catalyzed cross-coupling reaction of thioglycosides with (hetero)aryl halides

α- and β-thioglycosides serve as effective nucleophiles for Buchwald-Hartwig cross-coupling reactions using functionalized (hetero)aryl halides. The functional group tolerance on the electrophilic partner is typically high, both benzyl and acetate protect

Thio-arylglycosides with various aglycon para-substituents: A probe for studying chemical glycosylation reactions

Three series of thioglycosyl donors differing only in their respective aglycon substituents within each series have been prepared as representatives of typical glycosyl donors. The relative anomeric reactivities of these donors were quantified under compe

Formation and stability of oxocarbenium ions from glycosides

Structural, protecting group and leaving group effects in the formation of oxocarbenium intermediates were studied in the gas phase. It is found that significant stabilization of oxocarbenium cations is achieved by protecting groups that interact with the