87418-76-6

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 13089-48-0 N₄-benzoylcytidine 
• 16640-05-4 1-(β-D-arabinofuranosyl)-N⁴-benzoylcytosine 

Downstream Products

• 81246-78-8 5'-dimethoxytrityl 3'-tert-butyldimethyl silyl N-benzoylcytidine 
• 129666-74-6 5’-O-(1,1-bis(4-methoxyphenyl)-1-phenylmethyl)-2’-O-tert-butyldimethylsilylcytidine 
• 81246-77-7 5'-O-(dimethoxytrityl)-2',3'-O-bis(tert-butyldimetylsilyl)-N⁴-benzoylcytidine 
• 132055-15-3 Carbonic acid (2R,3R,4R,5R)-2-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-3-yl ester tert-butyl ester 
• 110764-74-4 N⁴-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-methylcytidine 
• 373645-96-6 N-{1-[(2R,3S,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-tetrahydro-furan-2-yl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide 
• 81256-87-3 N-{1-[(2R,3S,4R,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-3-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-tetrahydro-furan-2-yl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide 
• 1453190-11-8 C₄₃H₄₉N₃O₈Si 
• 1453190-10-7 C₄₃H₄₉N₃O₈Si 
• 1277171-61-5 C₃₆H₄₁N₃O₁₂ 
• 1277171-77-3 C₄₃H₅₂N₃O₁₃PS₂ 
• 1277171-54-6 C₅₇H₅₉N₃O₁₄ 
• 1332728-53-6 4-N-benzoyl-1-(2-O-benzoyloxymethoxymethyl-5-O-dimethoxytrityl-β-D-ribofuranosyl)cytosine 
• 1332728-55-8 4-N-benzoyl-1-(3-O-benzoyloxymethoxymethyl-5-O-dimethoxytrityl-β-D-ribofuranosyl)cytosine 

Relevant academic research and scientific papers

Synthesis and biological evaluation of novel selenonucleosides

A series of novel selenonucleoside analogues with 1,4-oxaselenane as the carbohydrate fragment has been synthesized from their corresponding dimesylated seconucleosides treated with NaHSe solution and subsequent deprotection. The synthesized selenonucleos

Phosphoramidate dinucleosides as hepatitis C virus polymerase inhibitors

GC dinucleosides exhibiting a phosphoramidate internucleosidic linkage with neutral, amphiphile, positively or negatively charged side chains were synthesized. Their potential inhibitory effect on the hepatitis C virus (HCV) NS5B polymerase was evaluated

Antisense modulation of CDC14A expression

Antisense compounds, compositions and methods are provided for modulating the expression of CDC14A. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding CDC14A. Methods of using these compounds for modulation of CDC14A expression and for treatment of diseases associated with expression of CDC14A are provided.

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

New catalists and procedures for the dimethoxytritylation and selective silylation of ribonucleosides

Procedures have been developed for the selective formation of (a) 2',5'-silylated ribonucleosides and (b) 3',5'-silylated ribonucleosides.These procedures also permit the selective silylation at either the 2'- or 3'-position of dimethoxytritylated ribonuc