588730-45-4

Upstream product

• 100-39-0 benzyl bromide 
• 152488-25-0 phenyl 6-O-(tert-butyldimethylsilyloxy)-1-thio-α-D-mannopyranoside 
• 2936-70-1 (2R,3S,4S,5S,6R)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 13992-16-0 phenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-mannopyranoside 

Downstream Products

• 152488-26-1 phenyl 2,3,4-tri-O-benzyl-1-thio-α-D-mannopyranoside 
• 588730-46-5 allyl [2,3,4-tri-O-benzyl-6-O-(tert-butyldimethylsilyl)-α-D-mannopyranosyl]-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 588730-48-7 allyl (2,3,4-tri-O-benzyl-6-O-{[2-(benzyloxycarbonylamino)ethyl](2-cyanoethyl)phosphonato}-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 263893-89-6 allyl (2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Screening of Neu5Acα(2-6)gal isomer preferences of siglecs with a sialic acid microarray

Sialic acids (Sias) are important terminal sugars on cell surfaces involved in a wide range of protein-carbohydrate interactions. Hence, agents modulating sias-mediated protein interactions are promising inhibitors or vaccine candidates. Here, we report t

Studies directed toward the synthesis of protein-bound GPI anchor

Mannobioside-linked phosphoethanolamine 10, a prototype model of the GPI anchor, was synthesized via glycosidation of the monosaccharide donor and acceptor, and subsequent phosphorylation. In order to test the reactivity of the amino group involved in 10

A stereospecific approach towards the synthesis of 2-deoxy α- and β-glycosides based on a 1,2-ethyl (phenyl) thio group migration

Iodonium ion (NIS/TfOH)-assisted glycosylation of a sugar acceptor with properly protected ethyl (phenyl) 2-O-phenoxythiocarbonyl 1-thio-β-D-gluco- or 1-thio-α-D-mannopyranoside donors gives the respective 1,2-trans linked 2'-ethyl (phenyl) thio-2'-deoxy-α-D-manno- or β-D-glucopyranosides.