238402-95-4

Upstream product

• 157793-52-7 p-chlorophenyl 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl phosphonate 
• 50571-26-1 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 106-48-9 4-chloro-phenol 
• 772-79-2 4-chlorophenylphosphorodichloridate 
• 40615-39-2 5'-O-(4-4'-dimethoxytrityl)thymidine 
• 123-76-2 levulinic acid 
• 93134-37-3 5'-O-(4,4'-dimethoxytrityl)-3'-O-levulinoyl-2'-deoxythymidine 
• 78635-98-0 3'-O-levulinoylthymidine 
• 65062-60-4 4-chlorophenyl 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl phosphate 

Downstream Products

• 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 
• 171974-13-3 C₄₆H₅₁N₄O₁₆P 

Relevant academic research and scientific papers

31p NMR studies on oxidative transformations of aryl nucleoside h-phosphonate diesters

Various aspects of oxidative coupling of nucleoside aryl H-phosphonate diesters with nucleosides to produce important synthetic intermediates in the phosphotriester approach to oligonucleotide synthesis, dinucleoside aryl phosphotriesters, was investigated. Copyright

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