329279-56-3

Upstream product

• 329279-50-7 3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2'-O-(2,3-dibenzoyloxy)propyluridine 
• 329279-49-4 3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2'-O-allyl-O⁴-2-nitrophenyluridine 
• 207565-51-3 3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2'-O-(2,3-dihydroxypropyl)uridine 
• 143463-63-2 3’,5’-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2’-O-allyluridine 
• 108782-90-7 1-(3',5'-O-1,1,3,3-tetraisopropyl-1,3-disilyl)-β-D-ribofuranosyl-4-(2-nitrophenyl)-2-pyrimidinone 
• 613-90-1 benzoyl cyanide 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 329279-55-2 2'-O-(2,3-dibenzoyloxy)propyluridine 

Relevant academic research and scientific papers

Synthesis of modified nucleotide building blocks containing electrophilic groups in the 2′-position

Chemical syntheses of 2′-O-(allyloxycarbonyl)methyladenosine, 2′-0-(methoxycarbonyl)methyladenosine and 2′-O-(2,3-dibenzoyloxy)propyluridine 3′-2-cyanoethyl-N,N-diisopropyl phosphoramidite building blocks are described. These monomers were used successful