76958-58-2Relevant articles and documents
The photochemistry of thymidylyl-(3′-5′)-5-methyl-2′- deoxycytidine in aqueous solution
Celewicz, Lech,Mayer, Moriz,Shetlar, Martin D.
, p. 404 - 418 (2005)
The photochemistry of the dinudeoside monophosphate thymidylyl-(3′- 5′)-5-methyl-2′-deoxycytidine (Tpm5dC) has been studied in aqueous solution using both 254 nm and UV-B radiation. A variety of dinucleotide photoproducts containing 5-methyl-cy
ON THE PHOSPHORYLATION OF DEOXYRIBONUCLEOSIDES AND THE PROTECTION OF DEOXYGUANOSINE
Francois, P.,Hamoir, G.,Sonveaux, E.,Vermeersch, H.,Ma, Y.
, p. 821 - 824 (2007/10/02)
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Simplified Liquid-Phase Preparation of Four Decadeoxyribonucleotides and their Preliminary Spectroscopic Characterization
Denny, William A.,Leupin, Werner,Kearns, David R.
, p. 2372 - 2393 (2007/10/02)
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.