How to cite this paper
APA: Sarrafi, Y., Pazokie, F., Azizi, S., Alimohammadi, K., Mehrasbi, E & Chiani, E. (2014). Mesoporous SBA-15 nanoparticles: An efficient and eco-friendly Catalyst for one-pot synthesis of 3, 4-dihydropyrimidin-2(1H)-ones under solvent-free conditions. Current Chemistry Letters, 3(2), 97-102.
Chicago/Turabian: Sarrafi, Y., Pazokie, F., Azizi, S., Alimohammadi, K., Mehrasbi, E & Chiani, E. 2014. "Mesoporous SBA-15 nanoparticles: An efficient and eco-friendly Catalyst for one-pot synthesis of 3, 4-dihydropyrimidin-2(1H)-ones under solvent-free conditions." Current Chemistry Letters 3, no. 2 (2014): 97-102.
AMA: Sarrafi, Y., Pazokie, F., Azizi, S., Alimohammadi, K., Mehrasbi, E & Chiani, E. Mesoporous SBA-15 nanoparticles: An efficient and eco-friendly Catalyst for one-pot synthesis of 3, 4-dihydropyrimidin-2(1H)-ones under solvent-free conditions. Current Chemistry Letters. 2014;3(2):97-102.
References
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3. Hoang, V. D., Dang, T. P., Dinh, Q. K., et al. (2010). The synthesis of novel hybrid thiol- functionalized nano-structured SBA-15. Adv. Nat. Sci.: Nanosci. Nanotechnol., 1, 1-6.
4. Evans, D. A., Tedrow, J. S., Shaw, J. T., et al. (2002). Diastereoselective Magnesium Halide-Catalyzed anti-Aldol Reactions of Chiral N-Acyloxazolidinones. J. Am. Chem. Soc., 124, 392-393.
5. Tanaka, K. (2009). Solvent-free Organic Synthesis. WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim,.
6. Ramon, D. J., Yus, M. (2005). Asymmetric Multicomponent Reactions (AMCRs): The New Frontier. Angew. Chem., Int. Ed., 44, 1602-1634.
7. Ma, Y., Qian, C., Wang, L., et al. (2000). Lanthanide Triflate Catalyzed Biginelli Reaction. One- Pot Synthesis of Dihydropyrimidinones under Solvent- Free Conditions. J. Org. Chem., 65, 3864-3868.
8. Hu, E. H., Sidler, D. R., Dolling, U. H. (1998). Unprecedented Catalytic Three Component One-Pot Condensation Reaction:? An Efficient Synthesis of 5-Alkoxycarbonyl- 4-aryl-3, 4-dihydropyrimidin-2(1H)-ones. J. Org. Chem., 63, 3454-3457.
9.Snider, B. B., Shi, Z. (1993). Biomimetic synthesis of (±)-crambines A, B, C1, and C2. Revision of the structure of crambines B and C1. J. Org. Chem., 58, 3828-3839.
10. Fabian, W. M. F., Semones, M. A. (1997). Conformational analysis of 4-aryl-dihydropyrimidine calcium channel modulators. A comparison of ab initio, semiempirical and X-ray crystallographic studies. Tetrahedron, 53, 2803-2816.
11. Biginelli, P. (1893). Synthesis of dihydropyrimidinones. Gazz. Chim. Ital., 23, 360-413.
12. Hassani, Z., Islami, M. R., Kalantari, M. (2006). An efficient one-pot synthesis of octahydroquinazolinone derivatives using catalytic amount of H2SO4 in water. Bioorg. Med. Chem. Lett., 16, 4479-4482.
13. Silva, D. L. da., Fernandes, S. A., Sabino, A. A., et al. (2011). P-sulfonic acid calixarenes as efficient and reusable organocatalysts for the synthesis of 3, 4-dihydropyrimidin-2(1H)-ones/-thiones. Tetrahedron Lett., 52, 6328-6330.
14.Radha, Rani .V., Srinivas, N., Radha, Kishan. M., et al. (2001). Zeolite-catalyzed cyclocondensation reaction for the selective synthesis of 3, 4-dihydropyrimidin-2(1H)-ones. Green Chem., 3, 305-306.
15. Mistry, S. R., Joshi, R. S., Sahoo, S. K. (2011). Synthesis of dihydropyrimidiones using large pore zeolites. Catal. Lett., 141, 1541-1547.
16. a) Xu, L–W., Yang, M–S., Jiang, J–X., et al. (2007). Ionic liquid-functionalized SBA-15 mesoporous material: efficient heterogeneous catalyst in versatile organic reactions. Cent. Eur. J. Chem., 5, 1073- 1083; b) mondal, J., Sen, T., Bhaumik, A. (2012). Fe3O4@mesoporous SBA-15: a robust and magnetically recoverable catalyst for one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones viathe Biginelli reaction. Dalton trans., 41, 6173-6181.
17. Srivastava, R. (2010). Assessment of the catalytic activities of novel bronsted acidic ionic liquid catalysts. Catal. Lett., 139, 17-25.
18.Tajbakhsh, M., Mohammadpoor-Baltork, I., Alimohammadi, K. (2003). An Efficient and Selective Solid State Oxidation of Thiols to Disulfides with Quinolinium Fluorochromate on Silica Gel. Monat. Chem., 134, 1571-1575.
19. Sarrafi, Y., Mohadeszadeh, M., Alimohammadi, K. (2009). Microwave- assisted chemoselective copper-catalyzed amination of o-chloro and o-bromobenzoic acids using aromatic amines under solvent free conditions. Chin. Chem. Lett., 20, 784-788.
20. Azizi, S. N., ghasemi, Sh., Chiani, E. (2013). Nickel/mesoporous silica (SBA-15) modified electrode: An effective porous material for electrooxidation of methanol. Electrochim. Acta, 88, 463-472.
21. Su, W., Li, J., Zheng, Z., Shen, Y. (2005). One-pot synthesis of dihydropyrimidiones catalyzed by strontium (II) triflate under solvent-free conditions. Tetrahedron Lett., 46, 6037-6040.
22. Sun, Q., Wang, Y., Ge, Z., et al. (2004). A highly efficient solvent-free synthesis of dihydropyrimidinones catalyzed by zinc chloride. Synthesis, 7, 1047-1051.
23. Zorkun, I. S., Sarac, S., Semra, C.¸ et al. (2006). Synthesis of 4-aryl-3, 4-dihydropyrimidin-2(1H) –thiones derivatives as potential calcium channel blockers. Bioorg. Med. Chem., 14, 8582-8589.
24. Litvic, M., Vecenaj, I., Ladisic, Z. M. et al. (2010). First application of hexaaquaaluminium (III) tetrafluoroborate as a mild, recyclable, non-hygroscopic acid catalyst in organic synthesis: a simple and efficient protocol for the multigame scale synthesis of 3, 4-dihydropyrimidinones by Biginelli reaction. Tetrahedron, 66, 3463-3471.
25. Shaabani, A., Bazgir, A., Teimouri, F. (2003). Ammonium chloride- catalyzed one- pot synthesis of 3, 4- dihydropyrimidin-2(1H) - ones under solvent-free conditions. Tetrahedron Lett., 44, 857-859.
26. Salehi, P., Dabiri, M., Zolfigol, M. A., et al. (2003). Silica sulfuric acid: an efficient and reusable catalyst for the one-pot synthesis of 3, 4-dihydropyrimidin-2(1H) –ones. Tetrahedron Lett., 44, 2889-2891.
27. Lu, J., Bai, Y., Wang, Z., et al. (2000). One- pot synthesis of 3, 4-dihydropyrimidin-2(1H)-ones using lanthanum chloride as a catalyst. Tetrahedron Lett., 41, 9075-9078.
28.Ranu, B. C., Hajra, A., Jana, U. (2000). Indium (III) Chloride-Catalyzed One-Pot Synthesis of Dihydropyrimidinones by a Three-Component Coupling of 1,3-Dicarbonyl Compounds, Aldehydes, and Urea: An Improved Procedure for the Biginelli Reaction. J. Org. Chem., 65, 6270-6276.
29. Memarian, H. R., Sabzyan, H., Farhadi, A. (2009). Microwave-assisted oxidation of 3, 4-dihydropyrimidin-2(1H) –ones. Zeitschrift fur Naturforschung, 64, 532-540.
30. Fu, N-Y., Yuan, Y- F., Cao, Z., et al. (2002). Indium (III) bromide-catalyzed preparation of dihydropyrimidiones: improved protocol conditions for the niginelli reaction. Tetrahedron, 58, 4801-4807.
2. Tajbakhsh, M., Mohajerani, B., Heravi, M. M., et al. (2005). Natural HEU type zeolite catalyzed Biginelli reaction for the synthesis of 3, 4- dihydropyrimidin-2 (1H) one derivatives. J. Mol. Catal. A: Chem., 236, 216-219.
3. Hoang, V. D., Dang, T. P., Dinh, Q. K., et al. (2010). The synthesis of novel hybrid thiol- functionalized nano-structured SBA-15. Adv. Nat. Sci.: Nanosci. Nanotechnol., 1, 1-6.
4. Evans, D. A., Tedrow, J. S., Shaw, J. T., et al. (2002). Diastereoselective Magnesium Halide-Catalyzed anti-Aldol Reactions of Chiral N-Acyloxazolidinones. J. Am. Chem. Soc., 124, 392-393.
5. Tanaka, K. (2009). Solvent-free Organic Synthesis. WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim,.
6. Ramon, D. J., Yus, M. (2005). Asymmetric Multicomponent Reactions (AMCRs): The New Frontier. Angew. Chem., Int. Ed., 44, 1602-1634.
7. Ma, Y., Qian, C., Wang, L., et al. (2000). Lanthanide Triflate Catalyzed Biginelli Reaction. One- Pot Synthesis of Dihydropyrimidinones under Solvent- Free Conditions. J. Org. Chem., 65, 3864-3868.
8. Hu, E. H., Sidler, D. R., Dolling, U. H. (1998). Unprecedented Catalytic Three Component One-Pot Condensation Reaction:? An Efficient Synthesis of 5-Alkoxycarbonyl- 4-aryl-3, 4-dihydropyrimidin-2(1H)-ones. J. Org. Chem., 63, 3454-3457.
9.Snider, B. B., Shi, Z. (1993). Biomimetic synthesis of (±)-crambines A, B, C1, and C2. Revision of the structure of crambines B and C1. J. Org. Chem., 58, 3828-3839.
10. Fabian, W. M. F., Semones, M. A. (1997). Conformational analysis of 4-aryl-dihydropyrimidine calcium channel modulators. A comparison of ab initio, semiempirical and X-ray crystallographic studies. Tetrahedron, 53, 2803-2816.
11. Biginelli, P. (1893). Synthesis of dihydropyrimidinones. Gazz. Chim. Ital., 23, 360-413.
12. Hassani, Z., Islami, M. R., Kalantari, M. (2006). An efficient one-pot synthesis of octahydroquinazolinone derivatives using catalytic amount of H2SO4 in water. Bioorg. Med. Chem. Lett., 16, 4479-4482.
13. Silva, D. L. da., Fernandes, S. A., Sabino, A. A., et al. (2011). P-sulfonic acid calixarenes as efficient and reusable organocatalysts for the synthesis of 3, 4-dihydropyrimidin-2(1H)-ones/-thiones. Tetrahedron Lett., 52, 6328-6330.
14.Radha, Rani .V., Srinivas, N., Radha, Kishan. M., et al. (2001). Zeolite-catalyzed cyclocondensation reaction for the selective synthesis of 3, 4-dihydropyrimidin-2(1H)-ones. Green Chem., 3, 305-306.
15. Mistry, S. R., Joshi, R. S., Sahoo, S. K. (2011). Synthesis of dihydropyrimidiones using large pore zeolites. Catal. Lett., 141, 1541-1547.
16. a) Xu, L–W., Yang, M–S., Jiang, J–X., et al. (2007). Ionic liquid-functionalized SBA-15 mesoporous material: efficient heterogeneous catalyst in versatile organic reactions. Cent. Eur. J. Chem., 5, 1073- 1083; b) mondal, J., Sen, T., Bhaumik, A. (2012). Fe3O4@mesoporous SBA-15: a robust and magnetically recoverable catalyst for one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones viathe Biginelli reaction. Dalton trans., 41, 6173-6181.
17. Srivastava, R. (2010). Assessment of the catalytic activities of novel bronsted acidic ionic liquid catalysts. Catal. Lett., 139, 17-25.
18.Tajbakhsh, M., Mohammadpoor-Baltork, I., Alimohammadi, K. (2003). An Efficient and Selective Solid State Oxidation of Thiols to Disulfides with Quinolinium Fluorochromate on Silica Gel. Monat. Chem., 134, 1571-1575.
19. Sarrafi, Y., Mohadeszadeh, M., Alimohammadi, K. (2009). Microwave- assisted chemoselective copper-catalyzed amination of o-chloro and o-bromobenzoic acids using aromatic amines under solvent free conditions. Chin. Chem. Lett., 20, 784-788.
20. Azizi, S. N., ghasemi, Sh., Chiani, E. (2013). Nickel/mesoporous silica (SBA-15) modified electrode: An effective porous material for electrooxidation of methanol. Electrochim. Acta, 88, 463-472.
21. Su, W., Li, J., Zheng, Z., Shen, Y. (2005). One-pot synthesis of dihydropyrimidiones catalyzed by strontium (II) triflate under solvent-free conditions. Tetrahedron Lett., 46, 6037-6040.
22. Sun, Q., Wang, Y., Ge, Z., et al. (2004). A highly efficient solvent-free synthesis of dihydropyrimidinones catalyzed by zinc chloride. Synthesis, 7, 1047-1051.
23. Zorkun, I. S., Sarac, S., Semra, C.¸ et al. (2006). Synthesis of 4-aryl-3, 4-dihydropyrimidin-2(1H) –thiones derivatives as potential calcium channel blockers. Bioorg. Med. Chem., 14, 8582-8589.
24. Litvic, M., Vecenaj, I., Ladisic, Z. M. et al. (2010). First application of hexaaquaaluminium (III) tetrafluoroborate as a mild, recyclable, non-hygroscopic acid catalyst in organic synthesis: a simple and efficient protocol for the multigame scale synthesis of 3, 4-dihydropyrimidinones by Biginelli reaction. Tetrahedron, 66, 3463-3471.
25. Shaabani, A., Bazgir, A., Teimouri, F. (2003). Ammonium chloride- catalyzed one- pot synthesis of 3, 4- dihydropyrimidin-2(1H) - ones under solvent-free conditions. Tetrahedron Lett., 44, 857-859.
26. Salehi, P., Dabiri, M., Zolfigol, M. A., et al. (2003). Silica sulfuric acid: an efficient and reusable catalyst for the one-pot synthesis of 3, 4-dihydropyrimidin-2(1H) –ones. Tetrahedron Lett., 44, 2889-2891.
27. Lu, J., Bai, Y., Wang, Z., et al. (2000). One- pot synthesis of 3, 4-dihydropyrimidin-2(1H)-ones using lanthanum chloride as a catalyst. Tetrahedron Lett., 41, 9075-9078.
28.Ranu, B. C., Hajra, A., Jana, U. (2000). Indium (III) Chloride-Catalyzed One-Pot Synthesis of Dihydropyrimidinones by a Three-Component Coupling of 1,3-Dicarbonyl Compounds, Aldehydes, and Urea: An Improved Procedure for the Biginelli Reaction. J. Org. Chem., 65, 6270-6276.
29. Memarian, H. R., Sabzyan, H., Farhadi, A. (2009). Microwave-assisted oxidation of 3, 4-dihydropyrimidin-2(1H) –ones. Zeitschrift fur Naturforschung, 64, 532-540.
30. Fu, N-Y., Yuan, Y- F., Cao, Z., et al. (2002). Indium (III) bromide-catalyzed preparation of dihydropyrimidiones: improved protocol conditions for the niginelli reaction. Tetrahedron, 58, 4801-4807.