Recent Developments in the Synthetic Strategies of 4-Quinolones and Its Derivatives

被引:16
作者
Singh, Gurpreet [1 ]
Devi, Varsha [1 ]
Monga, Vikramdeep [1 ]
机构
[1] ISF Coll Pharm, Dept Pharmaceut Chem, GT Rd, Moga 142001, Punjab, India
来源
CHEMISTRYSELECT | 2020年 / 5卷 / 44期
关键词
4-Quinolones; C− H activation; Enantioselective Synthesis; Inorganic Catalysis; Metal-assisted synthesis; Visible light Oxidation; C-H AMIDATION; ANTIBACTERIAL EVALUATION; BIOLOGICAL EVALUATION; MOLECULAR DOCKING; FACILE SYNTHESIS; FLUOROQUINOLONE; ANTIOXIDANT; NEMONOXACIN; CYCLIZATION; INHIBITION;
D O I
10.1002/slct.202003570
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ubiquitous presence of 4-quinolones and its derivatives in a wide range of natural as well as synthetic drug molecules made them molecule of utmost importance for organic and medicinal chemists. Their wide array of biological activities such as antimicrobial, anticancer, anti-HIV, genitourinary infection, antifilarial, etc., has augmented their appeal both for synthetic and medicinal chemistry campaigns. Moreover, they are valuable intermediates for the synthesis of various fused heterocyclic compounds of synthetic and medicinal importance. Considering their array of synthetic and biological importance, new strategies for the synthesis of 4-quinolones and their derivatives have been designed and successfully demonstrated by researchers around the globe. The present review covers recent advances in the synthetic chemistry of 4-quinolones since 2015 along with an insight into their mechanistic studies. We hope that the review article will serve as a valuable tool for the scientific community engaged in the synthesis and utilization of 4-quinolones and their derivatives.
引用
收藏
页码:14100 / 14129
页数:30
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