Lewis acidic mesoporous Fe-TUD-1 as catalysts for synthesis of Hantzsch 1,4-dihydropyridine derivatives
Source abstract
Abstract
Lewis acidic mesoporous material (TUD-1) containing Fe was investigated as stable and reusable catalyst for the synthesis of Hantzsch 1,4-dihydropyridine (DHP) derivatives. Yields between 76 and 91 % of DHP derivatives were obtained in shorter reaction times of 3 h depending on the nature of substituents in benzaldehyde.
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Research context
OpenAlex topics: Multicomponent Synthesis of Heterocycles · Chemical Synthesis and Reactions · Microwave-Assisted Synthesis and Applications
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References (38)
Show source-provided references
1. A. Corma, H. García, Chem. Rev. 103, 4307 (2003)10.1021/cr030680z ↗
2. K. Wilson, J.H. Clark, Pure Appl. Chem. 72, 1313 (2000)10.1351/pac200072071313 ↗
3. M. Jose Climent, A. Corma, S. Iborra, RSC Adv 2, 16 (2012)10.1039/C1RA00807B ↗
4. S.D. Sawant, M. Srinivas, G. Lakshma Reddy, V. Venkateswar Rao, P.P. Singh, R.A. Vishwakarma, Tetrahedron Lett. 53, 6195 (2012)10.1016/j.tetlet.2012.08.137 ↗
5. M. Syamala, Org. Prep. Proced. Int. 41, 1 (2009)10.1080/00304940802711218 ↗
6. Z.-G. Cheng, X.-Y. Dai, L.-W. Li, Q. Wan, X. Ma, G.-Y. Xiang, Molecules 19, 1344 (2014)10.3390/molecules19011344 ↗
7. M. Filipan-Litvić, M. Litvić, I. Cepanec, V. Vinković, Molecules 12, 2546 (2007)10.3390/12112546 ↗
8. S. Wirtz, S. Herzig, Br. J. Pharmacol. 142, 275 (2004)10.1038/sj.bjp.0705786 ↗
9. J.-P. Wan, Y. Liu, RSC Adv. 2, 9763 (2012)10.1039/c2ra21406g ↗
10. Suresh, D. Kumar, J.S. Sandhu, Synth. Commun. 39, 1957 (2009)10.1080/00397910802622762 ↗
11. K.L. Bridgwood, G.E. Veitch, S.V. Ley, Org. Lett. 10, 3627 (2008)10.1021/ol801399w ↗
12. M.M. Heravi, B. Baghernejad, H.A. Oskooie, R. Hekmatshoar, Tetrahedron Lett. 49, 6101 (2008)10.1016/j.tetlet.2008.08.012 ↗
13. M.M. Heravi, K. Bakhtiari, N.M. Javadi, F.F. Bamoharram, M. Saeedi, H.A. Oskooie, J. Mol. Catal. Chem. 264, 50 (2007)10.1016/j.molcata.2006.09.004 ↗
14. H.G.O. Alvim, G.A. Bataglion, L.M. Ramos, A.L. de Oliveira, H.C.B. de Oliveira, M.N. Eberlin, J.L. de Macedo, W.A. da Silva, B.A.D. Neto, Appl. Org. Synth. 70, 3306 (2014)
15. N. Isambert, M. del M.S. Duque, J.-C. Plaquevent, Y. Genisson, J. Rodriguez, T. Constantieux, Chem. Soc. Rev. 40, 1347 (2011)10.1039/C0CS00013B ↗
16. R. Liu, J. Zhang, Asian J. Chem. 23, 1743 (2011)
17. B. Jahanbin, A. Davoodnia, H. Behmadi, N. Tavakoli-Hoseini, Bull. Korean Chem. Soc. 33, 2140 (2012)10.5012/bkcs.2012.33.7.2140 ↗
18. B.R.P. Kumar, P. Masih, C.R. Lukose, N. Abraham, D. Priya, R.M. Xavier, K. Saji, L. Adhikary, J. Heterocycl. Chem. 46, 336 (2009)10.1002/jhet.67 ↗
19. R. Surasani, D. Kalita, A.V.D. Rao, K. Yarbagi, K.B. Chandrasekhar, J. Fluor. Chem. 135, 91 (2012)10.1016/j.jfluchem.2011.09.005 ↗
20. P.P. Ghosh, P. Mukherjee, A.R. Das, RSC Adv. 3, 8220 (2013)10.1039/c3ra40706c ↗
21. R. Pagadala, S. Maddila, V.D.B.C. Dasireddy, S.B. Jonnalagadda, Catal. Commun. 45, 148 (2014)10.1016/j.catcom.2013.11.012 ↗
22. A.M. Zonouz, S.B. Hosseini, Synth. Commun. 38, 290 (2008)10.1080/00397910701750003 ↗
23. M. Nasr-Esfahani, S.J. Hoseini, M. Montazerozohori, R. Mehrabi, H. Nasrabadi, J. Mol. Catal. Chem. 382, 99 (2014)10.1016/j.molcata.2013.11.010 ↗
24. N. Ahmed, Z.N. Siddiqui, J. Mol. Catal. Chem. 394, 232 (2014)10.1016/j.molcata.2014.07.015 ↗
25. A. Heydari, S. Khaksar, M. Tajbakhsh, H.R. Bijanzadeh, J. Fluor. Chem. 130, 609 (2009)10.1016/j.jfluchem.2009.03.014 ↗
26. S. Ghosh, F. Saikh, J. Das, A.K. Pramanik, Tetrahedron Lett. 54, 58 (2013)10.1016/j.tetlet.2012.10.079 ↗
27. P.P. Ghosh, S. Paul, A.R. Das, Tetrahedron Lett. 54, 138 (2013)10.1016/j.tetlet.2012.10.106 ↗
28. M.P. Pachamuthu, K. Shanthi, R. Luque, A. Ramanathan, Green Chem. 15, 2158 (2013)10.1039/c3gc40792f ↗
29. K. Kandasamy, M.P. Pachamuthu, M. Muthusamy, S. Ganesabaskaran, A. Ramanathan, RSC Adv. 3, 25367 (2013)10.1039/c3ra43913e ↗
30. M.P. Pachamuthu, V.V. Srinivasan, R. Maheswari, K. Shanthi, A. Ramanathan, Appl. Catal. Gen. 462–463, 143 (2013)10.1016/j.apcata.2013.05.008 ↗
31. M.P. Pachamuthu, S. Karthikeyan, G. Sekaran, R. Maheswari, A. Ramanathan, Clean: Soil Air Water 43, 375–381 (2015)
32. A. Debache, W. Ghalem, R. Boulcina, A. Belfaitah, S. Rhouati, B. Carboni, Tetrahedron Lett. 50, 5248 (2009)10.1016/j.tetlet.2009.07.018 ↗
33. C.A. Antonyraj, S. Kannan, Appl. Catal. Gen. 338, 121 (2008)10.1016/j.apcata.2007.12.028 ↗
34. S. Haddoum, I. Fechete, B. Donnio, F. Garin, D. Lutic, C.E. Chitour, Catal. Commun. 27, 141 (2012)10.1016/j.catcom.2012.07.009 ↗
35. M. S. Hamdy, G. Mul, J. C. Jansen, A. Ebaid, Z. Shan, A. R. Overweg, and T. Maschmeyer, Catal. Sustain. Future 11th Nord. Symp. Catal. 100, 255 (2005)10.1016/j.cattod.2004.10.018 ↗
36. M. Akçay, Appl. Catal. Gen. 294, 156 (2005)10.1016/j.apcata.2005.07.019 ↗
37. D.M. Do, S. Jaenicke, G.-K. Chuah, Catal. Sci. Technol. 2, 1417 (2012)10.1039/c2cy20084h ↗
38. N. Koukabi, E. Kolvari, A. Khazaei, M.A. Zolfigol, B. Shirmardi-Shaghasemi, H.R. Khavasi, Chem. Commun. 47, 9230 (2011)10.1039/c1cc12693h ↗