Mesoporous nanocrystalline MgAl2O4: A new heterogeneous catalyst for the synthesis of 2,4,6-triarylpyridines under solvent-free conditions

Chemical Papers

Volumn 67, Issue 7, 2013, Pages 688-695

  Safari, Javad ^a   Zarnegar, Zohre ^a   Borujeni, Mahmoud Borjian ^a  

^a UNIVERSITY OF KASHAN   (Iran)

Author keywords

heterogeneous catalyst; multicomponent reactions; nanocrystalline magnesium aluminate; one pot synthesis; solvent free

Indexed keywords

EID: 84879688017     PISSN: 03666352     EISSN: 13369075     Source Type: Journal    
DOI: 10.2478/s11696-013-0361-5     Document Type: Article

References (19)

1. Adib, M., Tahermansouri, H., Koloogani, S. A., Mohammadi, B., & Bijanzadeh, H. R. (2006). Kröhnke pyridines: an efficient solvent-free synthesis of 2,4,6-triarylpyridines. Tetrahedron Letters, 47, 5957-5960. DOI: 10.1016/j.tetlet.2006.01.162.
2. Banerjee, S., & Sereda, G. (2009). One-step, three-component synthesis of highly substituted pyridines using silica nanoparticle as reusable catalyst. Tetrahedron Letters, 50, 6959-6962. DOI: 10.1016/j.tetlet.2009.09.137.
3. Barluenga, J., Jiménez-Aquino, A., Fernández, M. A., Aznar, F., & Valdés, C. (2008). Multicomponent and one-pot synthesis of trisubstituted pyridines through a Pd-catalyzed crosscoupling/ cross-coupling/cycloaddition sequence. Tetrahedron, 64, 778-786. DOI: 10.1016/j.tet.2007.10.112.
4. Chiu, C. F., Tang, Z. L., & Ellingboe, J. W. (1998). Solid-phase synthesis of 2,4,6-trisubstituted pyridines. Journal of Combinatorial Chemistry, 1, 73-77. DOI: 10.1021/cc980005g.
5. Constable, E. C., Housecroft, C. E., Neuburger, M., Phillips, D., Raithby, P. R., Schofield, E., Sparr, E., Tocher, D. A., Zehnder, M., & Zimmermann, Y. (2000). Development of supramolecular structure through alkylation of pendant pyridyl functionality. Journal of Chemical Society, Dalton Transactions, 13, 2219-2228. DOI: 10.1039/b000940g.
6. Davoodnia, A., Bakavoli, M., Moloudi, R., Tavakoli-Hoseini, N., & Khashi, M. (2010). Highly efficient, one-pot, solvent-free synthesis of 2,4,6-triarylpyridines using a Brønsted-acidic ionic liquid as reusable catalyst. Monatshefte für Chemie - Chemical Monthly, 141, 867-870. DOI: 10.1007/s00706-010-0329-x.
7. Enyedy, I. J., Sakamuri, S., Zaman, W. A., Johnson, K. M., & Wang, S. M. (2003). Pharmacophore-based discovery of substituted pyridines as novel dopamine transporter inhibitors. Bioorganic & Medicinal Chemistry Letters, 13, 513-517. DOI: 10.1016/s0960-894x(02)00943-5.
8. 4 spinel as catalyst support. Materials Letters, 58, 1920-1923. DOI: 10.1016/j.matlet.2003. 12.013.
9. Heravi, M. M., Bakhtiari, K., Daroogheha, Z., & Bamoharram, F. F. (2007). An efficient synthesis of 2,4,6-triarylpyridines catalyzed by heteropolyacid under solventfree conditions. Catalysis Communications, 8, 1991-1994. DOI: 10.1016/j.catcom.2007.03.028.
10. 4 as a binary ionic liquid. Comptes Rendus Chimie, 14, 441-445. DOI: 10.1016/j.crci.2010.10.002.
11. Kim, B. Y., Ahn, J. B., Lee, H. W., Kang, S. K., Lee, J. H., Shin, J. S., Ahn, S. K., Hong, C. I., & Yoon, S. S. (2004). Synthesis and biological activity of novel substituted pyridines and purines containing 2,4-thiazolidinedione. European Journal of Medicinal Chemistry, 39, 433-447. DOI: 10.1016/j.ejmech.2004.03.001.
12. Klimešová, V., Svoboda, M., Waisser, K., Pour, M., & Kaustová, J. (1999). New pyridine derivatives as potential antimicrobial agents. Il Farmaco, 54, 666-672. DOI: 10.1016/s0014-827x(99)00078-6.
13. Maleki, B., Azarifar, D., Veisi, H., Hojati, S. F., Salehabadi, H., & Nejat Yami, R. (2010). Wet 2,4,6-trichloro-1,3,5-triazine (TCT) as an efficient catalyst for the synthesis of 2,4,6-triarylpyridines under solvent-free conditions. Chinese Chemical Letters, 21, 1346-1349. DOI: 10.1016/j.cclet.2010. 06.028.
14. Montazeri, N., & Mahjoob, S. (2012). Highly efficient and easy synthesis of 2,4,6-triarylpyridines catalyzed by pentafluorophenylammonium triflate (PFPAT) as a new recyclable solid acid catalyst in solvent-free conditions. Chinese Chemical Letters, 23, 419-422. DOI: 10.1016/j.cclet.2012.01. 035.
15. 2 as a novel and recyclable catalyst for the synthesis of 2,4,6-triarylpyridines under solvent-free conditions. Catalysis Communications, 8, 1973-1976. DOI: 10.1016/j.catcom.2007.08.003.
16. 4 spinel via surfactant assisted precipitation route. Powder Technology, 198, 275-278. DOI: 10.1016/j.powtec.2009.11.019.
17. Pillai, A. D., Rathod, P. D., Franklin, P. X., Patel, M., Nivsarkar, M., Vasu, K. K., Padh, H., & Sudarsanam, V. (2003). Novel drug designing approach for dual inhibitors as anti-inflammatory agents: implication of pyridine template. Biochemical and Biophysical Research Communications, 301, 183-186. DOI: 10.1016/s0006-291x(02)02996-0.
18. Safari, J., Khalili, S. D., Rezaei, M., Banitaba, S., & Meshkani, F. (2010). Nanocrystalline magnesium oxide: a novel and efficient catalyst for facile synthesis of 2,4,5-trisubstituted imidazole derivatives. Monatshefte für Chemie - Chemical Monthly, 141, 1339-1345. DOI: 10.1007/s00706-010- 0397-y.
19. Safari, J., Banitaba, S. H., & Dehghan Khalili, S. (2011). Cobalt nanoparticles promoted highly efficient one pot fourcomponent synthesis of 1,4-dihydropyridines under solventfree conditions. Chinese Journal of Catalysis, 32, 1850-1855. DOI: 10.1016/s1872-2067(10)60295-1.