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首页> 外文期刊>RSC Advances >Synthesis of protected 2′-O-deoxyribonucleotides on a precipitative soluble support: a useful procedure for the preparation of trimer phosphoramidites
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Synthesis of protected 2′-O-deoxyribonucleotides on a precipitative soluble support: a useful procedure for the preparation of trimer phosphoramidites

机译:在沉淀溶解载体上合成保护的2'-O-脱氧核糖核苷酸:制备三聚磷酰胺的有用方法

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Tetrakis- O -(4-azidomethylphenyl)pentaerythritol, derivatized with 5′- O -(4,4′-dimethoxytrityl)-3′- O -{4-[2-(but-3-yn-1-ylamino)-2-oxoethoxy]phenoxyacetyl}thymidine, was used as a soluble support to assemble fully protected 2′- O -deoxyribonucleotide trimers by the phosphotriester chemistry. After the coupling and detritylation steps, the support-bound construct was purified by precipitation in MeOH. The trimers (TAT, AGT, TTA, CAT, GCT), in fully protected form, were released by a treatment with dilute methanolic K _(2) CO _(3) and filtered through a short silica gel column in 65–70% overall yield. Two of the trimers (CAT and GCT), prepared in 0.5 mmol scale, were converted to the corresponding phosphoramidites. The entire procedure for the preparation of trimer phosphoramidites proved straightforward and applicable for the large scale synthesis.
机译:四乙烯(4-氮杂甲基苯基)季戊四醇,用5'- O - (4,4'-二甲氧基TRITYL) - 3'-O - {4- [2-(除-3- yN-1- ylamino) - 2-氧代乙氧基]苯氧基乙酰基}胸苷,用作可溶性载体,通过磷酸霉酯化学组装完全保护的2'-氧氧核糖核苷酸三晶体。在偶联和偏移步骤之后,通过MeOH的沉淀纯化载体结合的构建体。以完全保护的形式,通过用稀甲醇K _(2)CO_(3)的处理释放完全保护的形式的三聚体(TAT,AGT,TTA,猫,GCT)并通过短硅胶柱在65-70%中过滤总屈服。用0.5mmol刻度制备的两个三聚体(CAT和GCT)转化为相应的磷酰胺。制备三聚磷酰胺的整个程序已经证明了直接和适用于大规模合成。

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