Biginelli Reaction: A Multi-Component Type of Reaction and Synthetic Advancement in the Synthesis of Bioactive Dihydropyrimidinone Derivatives

被引:2
|
作者
Ambatwar, Ramesh [1 ]
Gupta, Vaibhav [1 ]
Kumar, Sumit [1 ]
Khatik, Gopal L. [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res Raebareli, Dept Med Chem, New Transit Campus,Bijnor Sisendi Rd, Lucknow 226002, Uttar Pradesh, India
关键词
Multi-component reaction; Biginelli reaction; dihydropyrimidinones; synthetic methodology; bioactive; heterocyclic scaffolds; ONE-POT SYNTHESIS; BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY; GREEN SYNTHESIS; SOLVENT-FREE; CATALYST; ACID; INHIBITORS; EG5; NANOPARTICLES;
D O I
10.2174/1570193X20666230601093704
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Background In synthetic and medicinal chemistry, multi-component reactions (MCRs) are considered an essential tool in synthesizing bioactive heterocyclic scaffolds. These reactions have been strategically used in drug discovery and development because of ease and economy.Objective The current manuscript aims to highlight the importance of the Biginelli reaction in the synthesis of diverse dihydropyrimidinones with medicinal applications.Methods We searched various keywords, including "multicomponent reaction", "Biginelli reaction" and "dihydropyrimidinone" on "PubMed, PubChem, and google scholar" and collected the relevant articles for including the current work.Results Biginelli reaction involving ketoester, aldehyde, and urea is a high-yielding, atom-economical, environmentally benign reaction for developing a library of new dihydropyrimidinones to drive the process of drug discovery. Several developments were achieved with modifications of synthetic techniques, including C-H activation, coupling, cycloaddition, etc. Inclusively, these modifications give access to a wide range of dihydropyrimidinones.Conclusion The current review provides an overview of recent developments in the Biginelli reaction and insights into synthesizing bioactive dihydropyrimidinones.
引用
收藏
页码:811 / 832
页数:22
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