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喹啉合成的最新进展

Recent Progress in the Synthesis of Quinolines.

作者信息

Xuan Duc Dau

机构信息

Department of Chemistry, Institute of Natural Science, Vinh University, Vinh City, Vietnam.

出版信息

Curr Org Synth. 2019;16(5):671-708. doi: 10.2174/1570179416666190719112423.

Abstract

BACKGROUND

Quinoline-containing compounds present in both natural and synthetic products are an important class of heterocyclic compounds. Many of the substituted quinolines have been used in various areas including medicine as drugs. Compounds with quinoline skeleton possess a wide range of bioactivities such as antimalarial, anti-bacterial, anthelmintic, anticonvulsant, antiviral, anti-inflammatory, and analgesic activity. Due to such a wide range of applicability, the synthesis of quinoline derivatives has attracted a lot of attention of chemists to develop effective methods. Many known methods have been expanded and improved. Furthermore, various new methods for quinoline synthesis have been established. This review will focus on considerable studies on the synthesis of quinolines date which back to 2014.

OBJECTIVE

In this review, we discussed recent achievements on the synthesis of quinoline compounds. Some classical methods have been modified and improved, while other new methods have been developed. A vast variety of catalysts were used for these transformations. In some studies, quinoline synthesis reaction mechanisms were also displayed.

CONCLUSION

Many methods for the synthesis of substituted quinoline rings have been developed recently. Over the past five years, the majority of those reported have been based on cycloisomerization and cyclization processes. Undoubtedly, more imaginative approaches to quinoline synthesis will appear in the literature in the near future. The application of known methods to natural product synthesis is probably the next challenge in the field.

摘要

背景

天然和合成产品中含喹啉的化合物是一类重要的杂环化合物。许多取代喹啉已被用于包括医药在内的各个领域作为药物。具有喹啉骨架的化合物具有广泛的生物活性,如抗疟疾、抗菌、驱虫、抗惊厥、抗病毒、抗炎和镇痛活性。由于其广泛的适用性,喹啉衍生物的合成吸引了许多化学家的关注,以开发有效的方法。许多已知方法已得到扩展和改进。此外,还建立了各种喹啉合成的新方法。本综述将重点关注自2014年以来关于喹啉合成的大量研究。

目的

在本综述中,我们讨论了喹啉化合物合成的最新进展。一些经典方法已被改进和完善,同时也开发了其他新方法。这些转化过程使用了各种各样的催化剂。在一些研究中,还展示了喹啉合成反应机理。

结论

最近已经开发了许多合成取代喹啉环的方法。在过去五年中,大多数报道的方法都基于环异构化和环化过程。毫无疑问,在不久的将来,文献中将会出现更多富有想象力的喹啉合成方法。将已知方法应用于天然产物合成可能是该领域的下一个挑战。

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