65062-60-4

Upstream product

• 40615-39-2 5'-O-(4-4'-dimethoxytrityl)thymidine 
• 772-79-2 4-chlorophenylphosphorodichloridate 
• 50571-26-1 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 106-48-9 4-chloro-phenol 
• 157793-52-7 p-chlorophenyl 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl phosphonate 

Downstream Products

• 76859-58-0 <(MeO)2Tr>TpTOAc 
• 71459-58-0 5'-O-(bis(4-methoxyphenyl)phenylmethyl)-P-(4-chlorophenyl)thymidylyl-(3'->5')-2'-deoxy-N-(2-methyl-1-oxopropyl)guanosine 3'-benzoate 
• 71459-54-6 C₅₄H₅₂ClN₄O₁₅P 
• 73591-24-9 5'-O-(bis(4-methoxyphenyl)phenylmethyl)-P-(4-chlorophenyl)thymidylyl-(3'->5')-2'-deoxy-N-(2-methyl-1-oxopropyl)-3'-guanylic acid, 4-chlorophenyl 2-cyanoethyl ester 
• 238402-95-4 C₅₂H₅₄ClN₄O₁₆P 
• 85057-27-8 Benzoic acid (2R,3S)-5-((R)-4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-{(4-chloro-phenoxy)-[(2R,3S,5R)-2-hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-phosphoryloxymethyl}-tetrahydro-furan-3-yl ester 
• 90827-16-0 C₃₉H₄₂Cl₂N₈O₁₅P₂ 
• 295311-89-6 C₄₈H₅₅N₄O₁₇P 
• 295311-86-3 C₃₁H₄₀N₅O₁₆PS 
• 295311-84-1 phosphoric acid 4,5-dimethoxy-2-nitro-benzyl ester 3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester 2-hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 295311-82-9 phosphoric acid 3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester 2-hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 2-nitro-benzyl ester 

Relevant academic research and scientific papers

Aryl H-phosphonates. Part 13. A new, general entry to aryl nucleoside phosphate and aryl nucleoside phosphorothioate diesters

The reaction of nucleoside H-phosphonate monoesters with phenols in the presence of a condensing agent, followed by oxidation of the in-situ-generated aryl nucleoside H-phosphonate diesters with iodine-water or with elemental sulfur, provides a new, 'one-

Synthesis and properties of photolabile (Caged) phosphotriester derivatives of dinucleoside phosphates

Dinucleoside phosphates that harbor phosphate groups transiently blocked (caged) by o-nitrobenzyl or o-nitroveratryl residues were synthesized. It was shown that the conditions of the UV-induced deprotection largely depend on the nature of the protective