铜催化C-S键形成反应合成硫杂环化合物的研究进展

Sanjukta Muhuri, H. Rahaman
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引用次数: 0

摘要

在大量具有生物活性的天然产物和药物中,重要的亚结构是含硫杂环。硫醚和其他富硫分子通常出现在化学生物学、有机合成和材料化学中。在形成碳杂原子键的情况下,铜催化的交叉偶联反应提供了一个强大的工具,因为它的成本低,并且在这里使用了易于获得和稳定的配体。铜催化C-S偶联反应是合成富硫杂环化合物的一种有效方法,因此得到了广泛的关注。综述了近年来以铜为催化剂合成含硫杂环化合物的研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent Developments in Synthesis of Sulfur Heterocycles via Copper-Catalyzed C-S Bond Formation Reaction
In a large number of biologically active natural products and pharmaceuticals, the important substructures are sulfur containing heterocycles. Thioethers and other sulphur-rich molecules commonly occur in chemical biology, organic synthesis and material chemistry. In case of the formation of carbon-heteroatom bonds, copper catalyzed cross-coupling reactions provide a powerful tool as its cost is low and here the readily accessible and stable ligands are used. It has been recognized that copper catalyzed C–S coupling reactions are an efficacious strategy for synthesizing sulfur-rich heterocyclic compounds and so the strategy has gained worldwide attention. This review sums up recent research developments in the field of synthesis of sulfur-containing heterocycles using copper-catalyst.
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