290359-93-2

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 3396-99-4 methyl α-D-galactopyranoside 

Downstream Products

• 3396-99-4 methyl α-D-galactopyranoside 
• 7432-72-6 Methyl 2,3,4-tri-O-acetyl-α-D-galactopyranoside 
• 181112-82-3 Succinic acid mono-{(2S,3R,4S,5S,6R)-3-acetoxy-5-benzoyloxy-6-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-methoxy-tetrahydro-pyran-4-yl} ester 
• 181112-81-2 Succinic acid mono-{(3aS,4R,6S,7R,7aS)-4-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-6-methoxy-2-phenyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl} ester 

Relevant academic research and scientific papers

Synthesis of multi-galactose-conjugated 2′-O-methyl oligoribonucleotides and their in vivo imaging with positron emission tomography

68Ga labelled 2′-O-methyl oligoribonucleotides (anti-miR-15b) bearing one, three or seven d-galactopyranoside residues have been prepared and their distribution in healthy rats has been studied by positron emission tomography (PET). To obtain t

Solid phase synthesis of oligosaccharides

An efficient and stereocontrolled solid-phase chemical synthesis of oligosaccarides using a new type of insoluble support (a copolymer of polyethylene glycol and polystyrene) is described. Several Lewis acids were tested as activators of the trichloroacetimidate 12, used as glycosyl donor, in the dimer 13 formation.