122591-36-0

Upstream product

• 169886-74-2 1-(2-O-acetyl-β-D-arabinofuranosyl)-uracil 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 69304-38-7 3',5'-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 
• 87418-79-9 5'-O-monomethoxytrityl-3'-O-tert-butyldimethylsilylarabinouridine 
• 104477-70-5 5',3'-O-(tetraisopropyldisiloxane-1,3-di-yl)-1-β-D-arabinofuranosyl-uracil 
• 169886-62-8 Acetic acid (2R,3S,3aR,9aR)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl ester 
• 84828-97-7 1-((6aR,8R,9aR)-2,2,4,4-tetraisopropyl-9-oxotetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)pyrimidine-2,4(1H,3H)-dione 

Downstream Products

• 112475-39-5 5'-O-monomethoxytritylarabinouridine-2'-O-acetyl-3'-O-N,N-diisopropyl-β-cyanoethylphosphoramidite 

Relevant academic research and scientific papers

Synthesis of oligoarabinonucleotides using H-phosphonates

Protected arabinonucleoside H-phosphonates have been prepared starting from ribonucleosides and used in solid phase synthesis of oligoarabinonucleotides.

Building blocks for synthesis of oligoarabinonucleotides: Preparation of arabinonucleoside H-phosphonates from protected ribonucleosides

A straightforward and inexpensive synthesis of arabinonucleoside H- phosphonates has been developed. Arabinonucleosides were synthesised from protected ribonucleosides via 2'-keto derivatives. Reaction conditions have been optimised for compounds hearing

Solution and solid phase chemical synthesis of arabinonucleotides

A fast and convenient procedure for the chemical synthesis of arabinonucleotides, which eliminates the multistep protection of the arabinonucleoside building blocks, is described.The results of these studies were successfully applied to the automated chem