喹啉
化学
抗真菌
组合化学
广谱
纳米技术
有机化学
皮肤病科
医学
材料科学
作者
Rukhsana Tabassum,Muhammad Ashfaq,Hiroyuki Oku
出处
期刊:Letters in Organic Chemistry
[Bentham Science]
日期:2020-10-21
卷期号:18 (9): 669-686
被引量:4
标识
DOI:10.2174/1570178617999201020215632
摘要
Synthesis of heterocyclic compounds containing quinoline scaffold gained significant attention of organic chemists due to their importance as a therapeutic agent in the pharmaceutical industry. Quinoline molecules exhibit extensive biological activities, a few of which are antiviral, anti-inflammatory antibacterial, antifungal, antiproliferative, anthelmintic and anticonvulsant. A variety of synthetic routes has been developed for construction compounds bearing the quinoline nucleus due to its broad spectrum of pharmacological activities. This review describes recent development in transition metal mediated synthetic protocols of these important heterocycles by the formation of quinoline rings or by substitution of quinoline rings, including both modified conventional name reactions and novel routes with highly functionalized quinoline products.
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