Department of Chemical Sciences, University of Naples Federico II, I-80126 Naples, Italy.
Department of Chemical, Materials and Production Engineering, University of Naples Federico II, I-80125 Naples, Italy.
Int J Mol Sci. 2024 Aug 20;25(16):9030. doi: 10.3390/ijms25169030.
The reagent system based on the combined use of EtSiH/I acts as an efficient -glycosidation promoter for the synthesis of natural and sugar-modified nucleosides. An analysis of reaction stereoselectivity in the absence of C2-positioned stereodirecting groups revealed high selectivity with six-membered substrates, depending on the nucleophilic character of the nucleobase or based on anomerization reactions. The synthetic utility of the EtSiH/I-mediated -glycosidation reaction was highlighted by its use in the synthesis of the investigational drug apricitabine.
基于 EtSiH/I 联合使用的试剂体系可作为一种有效的 -糖苷化促进剂,用于合成天然和糖修饰的核苷。在没有 C2 位立体定向基团的情况下,对反应立体选择性进行分析表明,对于六元底物具有很高的选择性,这取决于碱基的亲核性或基于端基异构化反应。EtSiH/I 介导的 -糖苷化反应的合成实用性通过其在研究药物阿匹卡韦的合成中的应用得到了强调。