220281-17-4

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 75-36-5 acetyl chloride 
• 220281-16-3 ethyl 6‐O‐tert‐butyldiphenylsilyl‐3,4‐O‐isopropylidene‐1‐thio‐β‐D‐galactopyranoside 
• 172146-95-1 ethyl 3,4-O-isopropylidene-1-thio-β-D-galactopyranoside 
• 108-24-7 acetic anhydride 

Downstream Products

• 696598-55-7 ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside 
• 696598-69-3 ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-O-acetyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 696598-76-2 ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2-O-acetyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 220281-18-5 ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside 

Relevant academic research and scientific papers

Synthesis of a Tetrasaccharide Related to the Repeating Unit of the Antigen from Shigella dysenteriae Type 9 in the Form of Its 2-(Trimethylsilyl)ethyl Glycoside

Starting from D-mannose, D-galactose and D-glucosamine hydrochloride, two disaccharide blocks were synthesized. Schmidt's inverse addition technique for trichloroacetimidate was utilized for the construction of a disaccharide with a β-mannosidic linkage i

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