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Catalytic Activity of Burkina Phosphates for Chalcone Synthesis in Green Solvent Cover

Catalytic Activity of Burkina Phosphates for Chalcone Synthesis in Green Solvent

Open Access
|Dec 2025

References

  1. Gruselle M. Apatites: A new family of catalysts in organic synthesis. J Organ Chem. 2015;793:93-101. DOI: 10.1016/j.jorganchem.2015.01.018.
  2. Su W, Cheng X, Shang S, Pan R, Qi M, Sang Q, et al. Advances in in situ investigations of heterogen catalytic ammonia synthesis. Catalysts. 2025;15:160. DOI: 10.3390/catal15020160.
  3. Friend CM, Xu B. Heterogen catalysis: A central science for a sustainable future. Acc Chem Res. 2017;50:517-21. DOI: 10.1021/acs.accounts.6b00510.
  4. Wacławek S, Padil VVT, Černík M. Major advances and challenges in heterogen catalysis for environmental applications: A review. Ecol Chem Eng S. 2018;25:9-34. DOI: 10.1515/eces-2018-0001.
  5. Zhou Y, Tian Y, Peng X. Applications and challenges of supercritical foaming technology. Polymers. 2023;15:402. DOI: 10.3390/polym15020402.
  6. Fallah A, Tajbakhsh M, Vahedi H, Bekhradnia A. Natural phosphate as an efficient and green catalyst for synthesis of tetraketone and xanthene derivatives. Res Chem Interm. 2017;43:29-43. DOI: 10.1007/s11164-016-2603-y.
  7. Ganesan M, Nagaraaj P. Recent developments in dehydration of primary amides to nitriles. Org Chem Front. 2020;7:3792-814. DOI: 10.1039/D0QO00843E.
  8. Riadi Y, Abrouki Y, Mamouni R, El Haddad M, Routier S, Guillaumet G, et al. New ecofriendly animal bone meal catalysts for preparation of chalcones and aza-Michael adducts. Chem Cent J. 2012;6:60. DOI: 10.1186/1752-153X-6-60.
  9. Yadav GD, Wagh DP. Claisen-Schmidt condensation using green catalytic processes: A critical review. Chem Select. 2020;5:9059-85. DOI: 10.1002/slct.202001737.
  10. Bentahar S, Taleb MA, Sabour A, Dbik A, Khomri ME, Messaoudi NE, et al. The use of modified clay as an efficient heterogeneous and ecofriendly catalyst for the synthesis of chalcones via Claisen-Schmidt condensation. Russ J Appl Chem. 2020;93:983-90. DOI: 10.1134/S107042722007006X.
  11. Devi K, Rajendran V, Ayushee, Rangarajan T, Singh R, Ghosh P, et al. Synthesis and evaluation of anti plasmodial activity of 2,2,2-trifluoroethoxychalcones and 2-fluoroethoxy chalcones against Plasmodium falciparum in culture. Molecules. 2018;23:1174. DOI: 10.3390/molecules23051174.
  12. Viana GSB, Bandeira MAM, Matos FJA. Analgesic and antiinflammatory effects of chalcones isolated from Myracrodruon urundeuva Allemão. Phytomedicine. 2003;10:189-95. DOI: 10.1078/094471103321659924.
  13. Marcovicz C, Camargo GDA, Scharr B, Sens L, Levandowski MN, Rozada TDC, et al. Schistosomicidal evaluation of synthesized bromo and nitro chalcone derivatives. J Mol Structure. 2022;1258:132647. DOI: 10.1016/j.molstruc.2022.132647.
  14. Borane N, Deshmukh AG, Oza NH, Boddula R, Patel PN. Newer chalcone scaffolds with reactive functional groups: Process, spectral and single crystal XRD studies. Eur J Chem. 2023;14:297-302. DOI: 10.5155/eurjchem.14.2.297-302.2405.
  15. Elazarifi N, Ezzamarty A, Leglise J, Ménorval LCD, Moreau C. Kinetic study of the condensation of benzaldehyde with ethylcyanoacetate in the presence of Al-enriched fluoroapatites and hydroxyapatites as catalysts. Appl Catal A: General. 2004;267:235-40. DOI: 10.1016/j.apcata.2004.03.012.
  16. Zăvoianu R, Tudorache M, Parvulescu VI, Cojocaru B, Pavel OD. New MgFeAl-LDH catalysts for Claisen-Schmidt condensation. Molecules. 2022;27:8391. DOI: 10.3390/molecules27238391.
  17. Aichi Y. Natural phosphate doped by potassium as efficient catalyst for the synthesis of chalcones by Claisen-Schmidt condensation reaction. Twist J. 2024;19:113-22. DOI: 10.5281/zenodo.10049652#74.
  18. Petigny L, Özel MZ, Périno S, Wajsman J, Chemat F. Water as green solvent for extraction of natural products. Chapter 7 in: Chemat F, Strube J, editors. Green Extraction of Natural Products: Theory and Practice. Willey; 2015:237-64. DOI: 10.1002/9783527676828.ch7.
  19. Mohammadi ZG, Badiei A, Abbasi A, Farahani Z. Cross-aldol condensation of cycloalkanones and aromatic aldehydes in the presence of nanoporous silica-based sulfonic acid (SiO2-Pr-SO3H) under solvent free conditions. Chin J Chem. 2009;27:1537-42. DOI: 10.1002/cjoc.200990259.
  20. Zoungrana JB, Sorgho B, Bakouan C, Sawadogo S, Ouedraogo RD, Guel B, et al. Mineralogical study of phosphate rocks by quantitative rietveld refinement. Open Ceramics. 2024;18:100567. DOI: 10.1016/j.oceram.2024.100567.
  21. Laasri L, Hadidi M. Eco-friendly procedure for the synthesis of 4-(Phenylamino)pent-3-en-2-one using an heterogen catalyst - ZnCl2/natural phosphate. Materials Today Proc. 2021;45:7352-8. DOI: 10.1016/j.matpr.2021.01.018.
  22. Widayat W, Hadiyanto H, Wardani PWA, Az Zuhra U, Prameswari J. Preparation of KI/hydroxyapatite catalyst from phosphate rocks and its application for improvement of biodiesel production. Molecules. 2020;25:2565. DOI: 10.3390/molecules25112565.
  23. Zahouily M, Mezdar A, Elmakssoudi A, Rayadh A, Sebti S, Lazrek HB. Comparison of different Lewis acids supported on natural phosphate as new catalysts for chemoselective dithioacetalization of carbonyl compounds under solvent-free conditions. Arkivoc. 2005;2006:31-40. DOI: 10.3998/ark.5550190.0007.203.
  24. Bazi F, Mounir B, Hamza M, Sebti S. A mild and efficient method for the synthesis of acylals from aromatic aldehydes and their deprotections catalyzed by synthetic phosphates under solvent-free conditions. Green Sust Chem. 2018;08:334-44. DOI: 10.4236/gsc.2018.84023.
  25. Mahato BN, Krithiga T. Recent developments in metal-doped SBA-15 catalysts for heterogen catalysis and sustainable chemistry. Can J Chem. 2022;100:9-17. DOI: 10.1139/cjc-2021-0201.
  26. Saber A, Smahi A, Solhy A, Nazih R, Elaabar B, Maizi M, et al. Heterogen catalysis of Friedel-Crafts alkylation by the fluorapatite alone and doped with metal halides. J Mol Catal A: Chemical. 2003;202:229-37. DOI: 10.1016/S1381-1169(03)00186-9.
  27. Rao GS, Kumar BP, Hussain S, Bhanuchander P. Metal phosphates: Preparation, characterization and catalytic evolution for vapour phase dehydration of glycerol to acrolein. Adv Sci Eng Med. 2020;12:356-63. DOI: 10.1166/asem.2020.2507.
  28. Dikova T, Parushev I, Dunchev V, Yotsova R, Ismailov I, Ivanov I, et al. Influence of heat treatment on the phase composition of biphasic calcium phosphates for biomedical application. Cureus. 2025. DOI: 10.7759/cureus.83514.
  29. Achchar M, Lamonier C, Ezzamarty A, Lakhdar M, Leglise J, Payen E. New apatite-based supports prepared by industrial phosphoric acid for HDS catalyst synthesis. Chem Reports. 2009;12:677-82. DOI: 10.1016/j.crci.2008.11.011.
  30. Sebti S, Saber A, Rhihil A, Nazih R, Tahir R. Claisen-Schmidt condensation catalysis by natural phosphate. Appl Catal A: General. 2001;206:217-20. DOI: 10.1016/S0926-860X(00)00604-9.
  31. Rhihil A, Aichi Y, Zahouily M, Sebti S, El Guendouzi M. Apatite phosphate doped by cobalt as hight efficient catalyst of multi-component synthesis of therapeutic spiropyrimidine compound. Nat Prod Bioprospect. 2022;12:35. DOI: 10.1007/s13659-022-00359-8.
  32. Andrushkevich TV, Ovchinnikova EV. The role of water in selective heterogeneous catalytic oxidation of hydrocarbons. Molec Catal. 2020;484:110734. DOI: 10.1016/j.mcat.2019.110734.
  33. Wu H, Zhang R, Li J, Chang J, Liu Z, Chen J, et al. Experimental and kinetic studies on the conversion of glucose to levulinic acid catalyzed by synergistic Cr/HZSM-5 in GVL/H2O biphasic system. Catalysts. 2025;15:162. DOI: 10.3390/catal15020162.
  34. Anand R, Hegde SG, Rao BS, Gopinath CS. Catalytic synthesis of 2-methyl pyrazine over Zn-modified zeolites. Catal Com. 2002;84:265-72. DOI: 10.1016/S1566-7367(01)00064-4.
  35. Jioui I, Dânoun K, Solhy A, Jouiad M, Zahouily M, Essaid B, et al. Modified fluorapatite as highly efficient catalyst for the synthesis of chalcones via Claisen-Schmidt condensation reaction. J Industrial Eng Chem. 2016;39:218-25. DOI: 10.1016/j.jiec.2016.06.003.
  36. Straiton AJ, Parish JD, Smith JJ, Lowe JP, Johnson AL. Exploration of solid-state vs solution-state structure in contact ion pair systems: Synthesis, characterization, and solution-state dynamics of zinc diphenyl phosphate, [Zn{O2P(OPh)2}2], donor-base-supported complexes. Inorg Chem. 2023;62:4770-85. DOI: 10.1021/acs.inorgchem.2c03539.
  37. Solhy A, Tahir R, Sebti S, Skouta R, Bousmina M, Zahouily M, et al. Efficient synthesis of chalcone derivatives catalyzed by reusable hydroxyapatite. Appl Catal A: General. 2010;374:189-93. DOI: 10.1016/j.apcata.2009.12.008.
  38. Blanco S. Determination of absorptivity and formation constant of a chalcone association complex. Talanta. 1998;45:1103-9. DOI: 10.1016/S0039-9140(97)00209-9.
  39. Brovelli F, Toledo D, Ahumada G, Moreno Y. Substituted heterocyclic chalcones: electrochemical, spectroscopic and theoretical study. J Chil Chem Soc. 2022;67:5662-6. DOI: 10.4067/S0717-97072022000305662.
  40. Jumina J, Styaningrum RW, Siswanta D, Triono S, Priastomo Y, Harizal H, et al. Synthesis and preliminary evaluation of several chalcone derivatives as sunscreen compounds. Chemistry J Moldova. 2019;14:90-6. DOI: 10.19261/cjm.2019.624.
  41. Wijayanti LW, Swasono RT, Lee W, Jumina J. Synthesis and evaluation of chalcone derivatives as novel sunscreen agent. Molecules. 2021;26:2698. DOI: 10.3390/molecules26092698.
DOI: https://doi.org/10.2478/cdem-2025-0003 | Journal eISSN: 2084-4506 | Journal ISSN: 1640-9019
Language: English
Published on: Dec 12, 2025
Published by: Society of Ecological Chemistry and Engineering
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2025 Jean-Baptiste Zoungrana, Brahima Sorgho, Corneille Bakouan, Régie Dimanche Ouedraogo, Maurice François Gonon, Boubié Guel, Philippe Blanchart, published by Society of Ecological Chemistry and Engineering
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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