87418-75-5

Upstream product

• 98-88-4 benzoyl chloride 
• 87418-74-4 4-Amino-1-{(2R,3S,4S,5R)-3,4-dihydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-1H-pyrimidin-2-one 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 65-46-3 CYTIDINE 
• 147-94-4 arabinosyl cytosine 
• 16640-05-4 1-(β-D-arabinofuranosyl)-N⁴-benzoylcytosine 

Downstream Products

• 160186-52-7 N⁴-benzoyl-5'-O-monomethoxytritylarabinocytidine-3'-O-N,N-diiso-propyl-β-cyanoethylphosphoramidite 
• 87418-82-4 N-(1-{(2R,3S,4S,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-benzamide 
• 72409-30-4 N-(1-{(2R,3S,4R,5R)-3-(tert-Butyl-dimethyl-silanyloxy)-4-hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-benzamide 

Relevant academic research and scientific papers

Hybridization properties of oligoarabinonucleotides

3'-Phosphoramidite derivatives of arabinocytidine, arabinoadenosine, and arabinouridine were prepared and used for the solid-phase synthesis of oligoarabinonucleotides (arabinonucleic acid, or ANA). Thermal denaturation analysis and gel mobility shift ass

The preparation of protected arabinonucleosides

A general procedure is described for the preparation of protected arabinonucleosides.Protection at the 5'-position involves triphenylmethyl groups (DMT and MMT) while the tert-butyldimethylsilyl (TBDMS) group is used to protect the 2'- or 3'-positions.The