首页> 外文期刊>The Journal of Organic Chemistry >Pyrazolo[1,5?a]?1,3,5-triazine C?Nucleoside as Deoxyadenosine Analogue: Synthesis, Pairing, and Resistance to Hydrolysis
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Pyrazolo[1,5?a]?1,3,5-triazine C?Nucleoside as Deoxyadenosine Analogue: Synthesis, Pairing, and Resistance to Hydrolysis

机译:吡唑并[1,5?a]?1,3,5-三嗪C?核苷作为脱氧腺苷类似物:合成,配对和抗水解

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摘要

The synthesis of a pyrazolo[1,5-a]-1,3,5-triazine C-nucleoside (dA~(PT)), designed to form two hydrogen bonds with a complementary dT residue, is reported. Oligonucleotides including this dA nucleoside analogue possess basepairing properties similar to those of the parent oligonucleotide. This dA nucleoside analogue is more resistant to acidcatalyzed hydrolysis than dA.
机译:据报道,吡唑并[1,5-a] -1,3,5-三嗪C-核苷(dA〜(PT))的合成旨在设计成两个带有互补dT残基的氢键。包括该dA核苷类似物的寡核苷酸具有与亲本寡核苷酸相似的碱基配对性质。这种dA核苷类似物比dA更耐酸催化水解。

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