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首页> 外文期刊>Artificial DNA. PNA & XNA >A solid-phase CuAAC strategy for the synthesis of PNA containing nucleobase surrogates
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A solid-phase CuAAC strategy for the synthesis of PNA containing nucleobase surrogates

机译:用于合成含核碱基替代物的PNA的固相CuAAC策略

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摘要

The synthesis of an azide containing PNA monomer is described. The monomer was incorporated into two PNA sequences for the purpose of synthesizing an intercalating fluorophore-labeled PNA and a metal binding hairpin using a solid phase copper catalyzed azide-alkyne Huisgen cycloaddition (CuAAC). Click chemistry was performed using 2-ethynylfluorene or 1-ethynylpyrene to add a fluorophore to the PNA, which were tested for their ability to recognize an abasic site on a DNA target. A PNA hairpin possessing azide monomers at each termini was synthesized and reacted with 2-ethynylpyridine to form a hairpin that is stabilized by Ni~(2+).
机译:描述了含叠氮化物的PNA单体的合成。为了使用固相铜催化的叠氮化物-炔烃Huisgen环加成(CuAAC)合成插入荧光团标记的PNA和金属结合发夹,将单体掺入两个PNA序列中。使用2-乙炔基芴或1-乙炔基re进行点击化学反应,以向PNA添加荧光团,并测试它们识别DNA靶标上的脱碱基位点的能力。合成在每个末端具有叠氮化物单体的PNA发夹,并与2-乙炔基吡啶反应形成由Ni〜(2+)稳定的发夹。

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