185994-24-5

Upstream product

• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 108-98-5 thiophenol 
• 604-69-3 β-D-glucose pentaacetate 
• 13992-16-0 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 98-88-4 benzoyl chloride 
• 143436-69-5 phenyl 6-O-(tert-butyldiphenylsilyl)-1-thio-β-D-glucopyranoside 
• 4551-15-9 phenylthiotrimethylsilane 
• 211947-42-1 4-Hydroxy-benzoic acid (2S,3R,4S,5R,6R)-3,4,5-tris-benzoyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-pyran-2-yl ester 

Downstream Products

• 866719-69-9 2,3,4-tri-O-benzoyl-6-O-(tert-butyldiphenylsilyl)-α-D-glucopyranosyl trichloroacetimidate 
• 866719-67-7 C₂₉H₂₄Cl₃NO₉ 
• 185994-28-9 C₅₃H₅₂INO₁₂Si 

Relevant academic research and scientific papers

Solid-phase synthesis of oligosaccharides: Construction of a dodecasaccharide

Complicated oligosaccharides such as dodecasaccharide 1 can be constructed by a new solid-phase strategy. The attachment to the polymeric support (gray sphere) is through a photolabile linker (structure I), and thioglycosides serve as carbohydrate donors. Bn = benzyl, Bz = benzoyl.