The synthesis and purification of modified antisense of igodeoxyriboucleotides (MAO ) are des cribed. A new oligonucleotide purification method and a novel activating agent, dimethyl sulfoxide, for thecondensation reaction are used. EDTA has been attached covalently to the 5’ end of the oligodeoxyribonucleotides sequence via an ethylenediamine linker in basic triethylammonium solution, then chelated withthe metal ions such as Fe(Ⅱ), Co(Ⅱ) or Cu(Ⅱ). High performance liquid chromatorgaphy is used to separate and purify this kind of MAO, using double mobile phase, triethylammonium acetate and acetonitrile. Byusing this routine chemical synthesis method, EDTA can be linked to the 5’ terminus of oligodeoxyribonucleotedes of any desired length and sequence, forming chimeric MAOs.
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机译:Design, Synthesis and Characterization of Novel Sulfonamides Derivatives as Anticancer Agent Targeting EGFR TK, and Development of New Methods of Synthesis by Microwave Irradiation
机译:studies on asymmetric syntheses of Benzophenanthridine alkaloids and the Related spiro Compounds: studies on Chelidonine synthesis and Total synthesis of arnottins I and II