首页> 外文期刊>Russian Journal of Organic Chemistry >Reactions of Lithiated Allenes with Isothiocyanates:First Example of Hydrolysis of 2,3-Dihydropyridines as a Novel Synthetic Route to 5,6-Dihydropyridin-2(1H)-ones
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Reactions of Lithiated Allenes with Isothiocyanates:First Example of Hydrolysis of 2,3-Dihydropyridines as a Novel Synthetic Route to 5,6-Dihydropyridin-2(1H)-ones

机译:锂化异戊烯与异硫氰酸酯的反应:2,3-二氢吡啶水解为5,6-二氢吡啶-2(1H)-ones的新型合成路线的第一个例子

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摘要

Pyridine derivatives,including pyridinones and dihydropyridinones,are key structural fragments in many natural biologically active compounds and most important medical agents,specifically anti-HIV preparations [1].Therefore,search and design of radically new and simultaneously simple and highly efficient synthetic approaches to these compounds,as well as extension of their assortment,constitute an actual problem.
机译:吡啶衍生物,包括吡啶酮和二氢吡啶酮,是许多天然生物活性化合物和最重要的药物,尤其是抗HIV制剂中的关键结构片段[1]。因此,研究和设计了新颖且同时简单高效的合成方法。这些化合物及其种类的扩展构成了一个实际的问题。

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