76958-61-7

Upstream product

• 15074-54-1 2-chlorophenyl dichlorophosphate 
• 958-09-8 2'-deoxy-D-adenosine 
• 4546-72-9 N₆-benzoyl-2'-deoxyadenosine 
• 64723-02-0 N-benzoyl-3',5'-di-O-benzoyl-2'-deoxyadenosine 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 72351-28-1 2-chlorophenyl phosphordi(1H-1-[1,2,4]triazolide) 
• 64325-78-6 N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine 

Downstream Products

• 96404-97-6 2-chlorophenyl bis<2-cyanoethyl>phosphate 
• 80817-34-1 N-6-benzoyl-5'-O-(dimethoxytrityl)-2'-deoxyadenosine 3'-(o-chlorophenyl β-cyanoethyl phosphate) 
• 91593-10-1 C₄₆H₄₄Cl₂N₈O₁₄P₂ 
• 94940-31-5 C₆₀H₅₅Cl₂N₇O₁₆P₂*C₆H₁₅N 
• 78111-52-1 C₆₇H₆₃Cl₂N₁₁O₁₆P₂ 
• 78111-53-2 <(MeO)2Tr>ibG_dΦbzA_dΦ(CNEt) 
• 78111-49-6 C₆₃H₅₈Cl₂N₈O₁₆P₂ 
• 78111-50-9 C₆₉H₆₁Cl₂N₉O₁₆P₂ 
• 75269-18-0 N-benzoyl-5'-O-(bis(4-methoxyphenyl)phenylmethyl)-P-(2-chlorophenyl)-2'-deoxyadenylyl-(3'->5')-N-benzoyl-2'-deoxy-3'-cytidylic acid, 2-chlorophenyl 2-cyanoethyl ester 
• 85240-06-8 C₄₉H₄₃Cl₂N₁₁O₁₃P₂ 
• 85240-01-3 C₆₁H₅₅ClN₇O₁₄P 
• 85240-03-5 C₄₂H₄₀Cl₂N₈O₁₄P₂ 
• 73118-61-3 Benzoic acid (2R,3S,5R)-2-[[(2R,3S,5R)-5-(6-benzoylamino-purin-9-yl)-2-hydroxymethyl-tetrahydro-furan-3-yloxy]-(2-chloro-phenoxy)-phosphoryloxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 85240-02-4 C₆₀H₅₅Cl₂N₇O₁₆P₂ 

Relevant academic research and scientific papers

eoxyribonucleic Acids and Related Compounds. VIII. Solid-Phase Synthesis of Deoxyribooligonucleotides with 3'-Modification by Elongation in the 3'-Direction

Four dodecanucleotides dATGTTTCCCTCTpOAr (12a), dATGATGTGGTATpOAr (12b), dATGTTGCCCGTTpOAr (12c) and dATGTGTCTGCGGpOAr (12d) having the 3'-(o-chlorophenyl)phosphate moiety have been synthesized on a polymer support by elongation in the 3'-direction.The 5'

Simplified Liquid-Phase Preparation of Four Decadeoxyribonucleotides and their Preliminary Spectroscopic Characterization

Four self-complementary decadeoxyribonucleotides, dApTpApTpApTpApTpApT,dApTpApTpCpGpApTpApT, dApTpApTpGpCpApTpApT and dApApApApApTpTpTpTpT, were chemically synthesized by the phosphotriester procedure.Efforts were concentrated on keeping the procedure as simple as possible, concomitant with obtaining high-purity products at each step of the process.The decamers were elaborated from the 3'-end, starting with a 3'-O-benzoylated monomer according to the scheme: monomer + monomer -> dimer + dimer -> tetramer + dimer -> hexamer + tetramer -> decamer.Putity of intermediates and of the fully blocked decamers were monitored by chromatography and by 300-MHz 1H-NMR. spectroscopy.The deblocked decadeoxyribonucleotides were characterized by their UV., CD., and 1H-NMR. spectra.