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首页> 外文期刊>The Journal of Antibiotics: An International Journal >Synthesis of unique spirocyclic orthoester-type derivatives of isothiazolo[4,3-d]pyrimidine nucleosides
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Synthesis of unique spirocyclic orthoester-type derivatives of isothiazolo[4,3-d]pyrimidine nucleosides

机译:异噻唑洛[4,3-D]嘧啶核苷的独特螺环酯型衍生物的合成

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摘要

A set of unique nucleoside analogs, containing 'spirocyclic orthoester-type' scaffolds, were synthesized from a common isothiazolo[4,3-d]pyrimidine-riboside precursor. The key reaction, using 1,2-di-heteroatomic nucleophiles (e.g., 1,2-ethandithiol) and BF3 center dot OEt2, converts an exocyclic imine into the spirocyclic analogs. The novel structural scaffold is confirmed through the use of one-and two-dimensional H-1 and C-13 NMR experiments.
机译:从一种常见的异噻唑并[4,3-d]嘧啶核苷前体合成了一组独特的核苷类似物,包含“螺环原酯型”支架。关键反应是使用1,2-二杂原子亲核试剂(例如,1,2-乙二硫醇)和BF3中心dot OEt2,将一个外环亚胺转化为螺环类似物。通过一维和二维H-1和C-13核磁共振实验证实了这种新型结构支架。

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