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作为RNA类似物的氟化吲哚的合成。

Synthesis of fluorinated indoles as RNA analogues.

作者信息

Bozilović Jelena, Engels Joachim W

机构信息

Institute for Organic Chemistry and Chemical Biology, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2007;26(8-9):869-71. doi: 10.1080/15257770701505220.

Abstract

Nucleoside analogues are chemical means to investigate hydrogen bonds, base stacking, and solvation as the three predominant forces that are responsible for the stability of secondary structure of nucleic acids. To obtain deeper insight into the contributions of these interactions to RNA stability apart from the ones exerted by the predominant nucleosides we decided to synthesize some novel nucleic acid analogues where the nucleobases are replaced by fluoroindoles. Fluorinated indoles can be compared to fluorinated benzimidazoles to determine the role of nitrogen in five membered ring system. The synthesis of fluoroindole ribonucleosides is described here.

摘要

核苷类似物是研究氢键、碱基堆积和溶剂化作用的化学手段,这三种主要作用力决定了核酸二级结构的稳定性。为了更深入地了解这些相互作用对RNA稳定性的贡献,除了主要核苷所发挥的作用之外,我们决定合成一些新型核酸类似物,其中的核苷酸碱基被氟代吲哚所取代。可以将氟化吲哚与氟化苯并咪唑进行比较,以确定五元环系统中氮的作用。本文描述了氟代吲哚核糖核苷的合成方法。

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