169886-79-7

Upstream product

• 786624-54-2 Acetic acid (2R,3S,4R,5R)-2-(4-amino-2-oxo-2H-pyrimidin-1-yl)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-3-yl ester 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 169886-76-4 1-(2-O-acetyl-β-D-arabinofuranosyl)-N⁴-isobuturylcytosine 
• 169886-64-0 Acetic acid (2R,3S,3aR,9aR)-2-(4-isobutyrylamino-2-oxo-2H-pyrimidin-1-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl ester 
• 169886-60-6 N-[1-((2R,3S,3aS,9aR)-3-Hydroxy-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-2-oxo-1,2-dihydro-pyrimidin-4-yl]-isobutyramide 
• 153809-36-0 N⁴-isobutyryl-3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)-cytidine 

Relevant academic research and scientific papers

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

Synthesis of oligoarabinonucleotides using H-phosphonates

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