Recent Updates on Synthetic Strategies of Chalcone Scaffold and their Heterocyclic Derivatives | ||||
| Journal of advanced Biomedical and Pharmaceutical Sciences | ||||
| Article 2, Volume 6, Issue 3, July 2023, Page 124-132 PDF (1 MB) | ||||
| Document Type: Review Articles | ||||
| DOI: 10.21608/jabps.2023.198509.1184 | ||||
 View on SCiNiTO | ||||
| Authors | ||||
Mohamed M Amin1; Montaser Sh. A. Shaykoon1; Adel A Marzouk1; Eman A Beshr2; Gamal Aburahama  3
| ||||
| 1Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Al-Azhar University, Assiut 71524, Egypt | ||||
| 2Department of Medicinal Chemistry, Faculty of Pharmacy, Minia University, Minia-61519, Egypt | ||||
| 3Faculty of Pharmacy, Minia University, Minia Egypt | ||||
| Abstract | ||||
| Chalcones, α,β-unsaturated ketone linking two aromatic moieties gained noticeable attention in the medicinal chemistry area. Chalcone-scaffold construction has proceeded via verified chemical synthetic strategies, including condensation, coupling, olefination, acylation, reductive annulation, one-pot, and Fries’ rearrangement methods. Specific approaches have assisted chalcone combinations using microwave radiation and ultrasound waves to enhance synthetic conditions and amplify yields. Recently, chalcones have been investigated extensively as core structures in potent bioactive hybrids such as anticancer, antimicrobial, and others. In addition, chalcones serve as parent structures for synthesizing several bioactive heterocyclic derivatives comprising five-membered and six-membered rings. This review will discuss recent applications of chalcones' synthetic strategies, physical and chemical characters, biological activities, and chemical derivatization. | ||||
| Keywords | ||||
| Chalcones; Synthesis; Chemistry; Derivatization | ||||
|
Statistics Article View: 433 PDF Download: 754 |
||||
