Reference

1. Jasim HA, Nahar L, Jasim MA, et al. Chalcones: synthetic chemistry follows where nature leads. Biomolecules 2021;11(8):1203.
2. Tang YL, Zheng X, Qi Y, et al. Synthesis and anti-inflammatory evaluation of new chalcone derivatives bearing bispiperazine linker as IL-1? inhibitors. Bioorg Chem 2020;98:103748.               
3. Venkatesh T, Bodke YD, Kenchappa R, et al. Synthesis, antimicrobial and antioxidant activity of chalcone derivatives containing thiobarbitone nucleus. Med Chem 2016;6(7):440-8.
4. Narwal S, Kumar S, Verma PK. Synthesis and biological activity of new chalcone scaffolds as prospective antimicrobial agents. Res Chem Intermed 2021;47(4):1625-41.
5. Gan X, Wang Y, Hu D, et al. Design, synthesis, and antiviral activity of novel chalcone derivatives containing a purine moiety. Chin J Chem 2017;35(5):665-72.
6. Sashidhara KV, Avula SR, Mishra V, et al. Identification of quinoline-chalcone hybrids as potential antiulcer agents. Eur J Med Chem 2015;89:638-53.         
7. Gupta D, Jain DK. Chalcone derivatives as potential antifungal agents: Synthesis, and antifungal activity. J Adv Pharm Technol Res 2015;6(3):114.      
8. Bonakdar AP, Vafaei F, Farokhpour M, et al. Synthesis and anticancer activity assay of novel chalcone-sulfonamide derivatives. Iran J Pharm Res 2017;16(2):565.
9. Gomes MN, Braga RC, Grzelak EM, et al. QSAR-driven design, synthesis and discovery of potent chalcone derivatives with antitubercular activity. Eur J Med Chem 2017;137:126-38.
10. Tomar V, Bhattacharjee G, Rajakumar S, et al. Synthesis of new chalcone derivatives containing acridinyl moiety with potential antimalarial activity. Eur J Med Chem 2010;45(2):745-51.
11. Hsieh CT, Hsieh TJ, El-Shazly M, et al. Synthesis of chalcone derivatives as potential anti-diabetic agents. Bioorg Med Chem Lett 2012;22(12):3912-5.
12. Alonso L, Menegatti R, Gomes RS, et al. Antileishmanial activity of the chalcone derivative LQFM064 associated with reduced fluidity in the parasite membrane as assessed by EPR spectroscopy. Eur J Pharm Sci 2020;151:105407.
13. Alberton EH, Damazio RG, Cazarolli LH, et al. Influence of chalcone analogues on serum glucose levels in hyperglycemic rats. Chem Biol Interact 2008;171(3):355-62.
14. Bhargav A, Narendra B. Gowda, Pavan kumar C. Synthesis, characterization and biological evaluation of substituted pyrimidines. Int j pharm res appl 2021;6;5,954-962.
15. Budak Y. Potassium tert?Butoxide Catalyzed Synthesis and Characterization of Novel 3?Aryl?3?(phenylthio)?1?(thiophen?3?yl) propan?1?one Derivatives. Chin J Chem 2012;30(2):341-4.
16. Kulkarni PS, Swami PM, Zubaidha PK. Calcium hydroxide is an efficient catalyst for synthesis of polyhydroxy chalcones. Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry. 2013;43(5):617-20.
17. Xin Y, Zang ZH, Chen FL. Ultrasound-promoted synthesis of 1, 5-diarylpenta-2, 4-dien-1-ones catalyzed by activated barium hydroxide. Synth Commun 2009;39(22):4062-8.
18. Won SJ, Liu CT, Tsao LT, et al. Synthetic chalcones as potential anti-inflammatory and cancer chemopreventive agents. Eur J Med Chem 2005;40(1):103-12.
19. Rosa GP, Seca AM, Barreto MD, et al. Chalcones and flavanones bearing hydroxyl and/or methoxyl groups: Synthesis and biological assessments. Appl Sci 2019;9(14):2846.
20. Sebti S, Solhy A, Smahi A, et al. Dramatic activity enhancement of natural phosphate catalyst by lithium nitrate. An efficient synthesis of chalcones. Catal Commun 2002;3(8):335-9.
21. Chand S, Sandhu JS. ZnO Nanoparticles: An efficient green reusable catalyst for the synthesis of 3-formyl benzopyranones chalcones by Claisen-Schmidt reaction under solvent-free condition. http://nopr.niscpr.res.in/handle/123456789/33037
22. Lyle RE, Paradis LP. Acid-catalyzed condensations. II. 1 the condensation of benzaldehyde with substituted acetophenones. J Am Chem Soc 1955;77(24):6667-8.
23. Narender T, Reddy KP. A simple and highly efficient method for the synthesis of chalcones by using borontrifluoride-etherate. Tetrahedron lett 2007;48(18):3177-80.
24. Hu Z, Liu J, Dong Z, et al. Synthesis of chalcones catalysed by SOCl2/EtOH. J Chem Res 2004;2004(2):158-9.
25. Adnan D, Singh B, Mehta SK, et al. Simple and solvent free practical procedure for chalcones: An expeditious, mild and greener approach. Curr Res Green Sustain Chem 2020;3:100041.
26. Sashidhara KV, Rosaiah JN, Kumar A. Iodine-catalyzed mild and efficient method for the synthesis of chalcones. Synth Commun 2009;39(13):2288-96.
27. Xu Q, Yang Z, Yin D, et al. Synthesis of chalcones catalyzed by a novel solid sulfonic acid from bamboo. Catal Commun 2008;9(7):1579-82.
28. Eddarir S, Cotelle N, Bakkour Y, et al. An efficient synthesis of chalcones based on the Suzuki reaction. Tetrahedron lett 2003;44(28):5359-63.
29. Wu XF, Neumann H, Beller M. Palladium?Catalyzed Coupling Reactions: Carbonylative Heck Reactions To Give Chalcones. Angew Chem 2010;122(31):5412-6.
30. Braun RU, Ansorge M, Müller TJ. Coupling–isomerization synthesis of chalcones. Chemistry– Eur J 2006;12(35):9081-94.
31. Zangade S, Mokle S, Vibhute A, et al. An efficient and operationally simple synthesis of some new chalcones by using grinding technique. Chem Sci J 2011;2(011).
32. Shntaif AH. Green synthesis of chalcones under microwave irradiation. Int J Chemtech Res 2016;9(02):36-9.
33. Li JT, Yang WZ, Chen GF, et al. A facile synthesis of ?, ??-bis (Substituted Benzylidene) cycloalkanones catalyzed by KF/Al2O3 under ultrasound irradiation. Synth Commun 2003;33(15):2619-25.
34. Li JT, Yang WZ, Wang SX, et al. Improved synthesis of chalcones under ultrasound irradiation. Ultrason Sonochem 2002;9(5):237-9.
35. Xu C, Chen G, Huang X. Chalcones by the Wittig reaction of a stable ylide with aldehydes under microwave irradiation. Org Prep Proced Int 1995;27(5):559-61.
36. Kumar A, Sharma S, Tripathi VD, et al. Synthesis of chalcones and flavanones using Julia–Kocienski olefination. Tetrahedron. 2010;66(48):9445-9.
37. Yoshizawa K, Shioiri T. Convenient stereoselective synthesis of (Z)-chalcone derivatives from 1, 3-diaryl-2-propynyl silyl ethers. Tetrahedron lett 2006;47(28):4943-5.