212128-08-0

Upstream product

• 105376-04-3 ethyl 2,3,4,6-tetra-O-benzoyl-1-thio-β-D-galactopyranoside 
• 139608-11-0 phenyl 2,3,4-tri-O-benzoyl-1-thio-β-D-galactopyranoside 
• 149707-75-5 2,3,4,6-tetra-O-benzoyl-1-O-trichloroacetimidoyl-α-D-galactopyranose 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-β-D-galactopyranose 
• 212128-07-9 phenyl 2,3,4-tri-O-benzoyl-6-O-tert-butyldimethytylsilyl-1-thio-β-D-galactopyranoside 
• 225241-29-2 phenyl 6-O-(tert-butyldimethylsilyloxy)-1-thio-β-D-galactopyranoside 
• 98-88-4 benzoyl chloride 
• 16758-34-2 1-thiophenyl-β-D-galactopyranoside 

Relevant academic research and scientific papers

Synthetic studies on glycosphingolipids from Protostomia phyla: Total syntheses of glycosphingolipids from the parasite, Echinococcus multilocularis

Efficient and systematic syntheses of four neutral glycosphingolipids that have been isolated from the metacestodes of Echinococcus multilocularis have been achieved. A key step is the direct glycosylation of galactosyl donors using thioglycosides with be

Scope and applications of "active and latent" thioglycosyl donors. Part 4

The relative reactivity of various thioglycosyl donors having ethyl, phenyl, or parasubstituted phenyl groups with electron donating (N-Ac) or electron withdrawing (NO2) substituents were compared using 1,2:3,4-di-O-isopropylidene-α-D-galactopy