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首页> 外文期刊>Journal of the American Chemical Society >Chemical Synthesis of Oligodeoxyribonucleotides Using N-Unprotected H-Phosphonate Monomers and Carbonium and Phosphonium Condensing Reagents: O-Selective Phosphonylation and Condensation
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Chemical Synthesis of Oligodeoxyribonucleotides Using N-Unprotected H-Phosphonate Monomers and Carbonium and Phosphonium Condensing Reagents: O-Selective Phosphonylation and Condensation

机译:使用N-未保护的H-膦酸酯单体和碳鎓和磷鎓缩合试剂的化学合成寡聚脱氧核糖核苷酸:O-选择性磷酰化和缩合

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摘要

Oligodeoxyribonucleotides were synthesized using H-phosphonate monomers without amino protection. The H-phosphonate monomers of deoxyadenosine, deoxycytidine, and deoxyguanosine bearing the free amino groups Were synthesized in good yields by O-selective phosphonylation of the parent 5'-O-(dimethoxytrityl)deoxyribonu- Cleosides.
机译:使用没有氨基保护的H-膦酸酯单体合成寡脱氧核糖核苷酸。带有游离氨基的脱氧腺苷,脱氧胞苷和脱氧鸟苷的H-膦酸酯单体是通过母体5'-O-(二甲氧基三苯甲基)脱氧核糖核苷-Cleosides的O-选择性膦酰化以高收率合成的。

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