220280-99-9

Upstream product

• 106-95-6 allyl bromide 
• 220280-97-7 methyl 4-S-(2-O'-acetyl-6-O'-tert-butyidiphenyisilyl-β-D-galacto-pyranosyl)mercaptobutyrate 
• 39257-91-5 methyl 4-mercaptobutanoate 
• 25878-60-8 D-galactose pentaacetate 
• 220280-95-5 methyl 4-S-(2-O'-acetyl-6-O'-tert-butyldiphenylsilyl-3,4-O'-isopropylidene-β-D-galactopyranosyl)mercaptobutyrate 
• 220280-93-3 4-[(3aS,4R,6S,7R,7aR)-4-(tert-Butyl-diphenyl-silanyloxymethyl)-7-hydroxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylsulfanyl]-butyric acid methyl ester 
• 220280-89-7 methyl 4-S-(6-O'-tert-butyldiphenylsilyl-beta-D-galactopyranosyl)mercaptobutyrate 
• 220280-85-3 methyl 4-S-(2',3',4',6'-tetra-O'-acetyl-beta-D-galactopyranosyl)mercaptobutyrate 
• 220280-91-1 methyl S-β-D-galactopyranosylmercaptobutyrate 

Downstream Products

• 220281-01-6 C₃₆H₅₂O₉SSi 

Relevant academic research and scientific papers

Substituted tetrahydropyrane derivatives, method for producing same, their use as medicine or diagnostic agent, as well as medicine containing same

Substituted tetrahydropyran derivatives, processes for their preparation, their use as a pharmaceutical or diagnostic, and pharmaceutical comprising them. The invention relates to compounds of the formula I in which the radicals R1, R2/su

Combinatorial solid-phase synthesis using D-galactose as a chiral five-dimension-diversity scaffold

All five hydroxy groups of galactose as the scaffold are used for selective coupling of side chains in a combinatorial methodology by application of a set of orthogonally stable protecting groups in combination with a thioglycoside anchor.