1242276-82-9

Upstream product

• 175911-73-6 (1-(benzyloxymethyl)cyclopent-3-enyl)methanol 
• 25878-60-8 D-galactose pentaacetate 
• 76910-02-6 3-cyclopenten-1,1-dimethanol 
• 1242276-80-7 (3-acetoxy-4-hydroxy-1-(hydroxymethyl)cyclopentyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 1242276-79-4 (3-acetoxy-1-(benzyloxymethyl)-4-hydroxycyclopentyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 1242276-78-3 (1-(benzyloxymethyl)-3,4-dihydroxycyclopentyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 1242165-01-0 (1-(benzyloxymethyl)cyclopent-3-enyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 108-30-5 succinic acid anhydride 
• 1242276-81-8 (3-acetoxy-1-O-(4,4'-dimethoxytrityl)methyl-4-hydroxycyclopentyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 

Relevant academic research and scientific papers

Simple solid-phase synthesis and biological properties of carbohydrate - Oligonucleotide conjugates modified at the 3′-terminus

A novel synthesis method for oligonucleotides possessing a functional moiety at the 3′-terminus was established based on solid-phase synthesis. In order to install the functional group at the 3′-terminus of the oligonucleotide, a solid support possessing