How to cite this paper
Moradi, F & Behbahani, F. (2018). Synthesis of arylidene dihydropyrimidinones and thiones catalyzed by iron (III) phosphate.Current Chemistry Letters, 7(3), 87-92.
Refrences
1. Atwal, K. S., Rovnyak, G.C., Reilly, B. C. Ó., and Schwartz, J. (1989) Substituted 1,4-dihydropyrimidines. III: Synthesis of selectively functionalized 2-hetero-1,4-dihydropyrimidines. J. Org. Chem., 54(25), 5898-5907.
2. Kappe, C.O., Fabian, W.M.F., and 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(8), 2803-2816.
3. Rashad, A. E., Shamroukh, A.H., Yousif, N. M., Salama, M.A.; Ali, H.S.; Ali, M. M., Mahmoud, A.E., and El-Shahat, M. (2012) New pyrimidinone and fused pyrimidinone derivatives as potential anticancer chemotherapeutics. Archiv der Pharmazie, 345(9), 729-738.
4. El-Subbagh, H. I., Abu-Zaid, S. M., Mahran, M. A., Badria, F. A., and Al-Obaid, A. M. (2000) Synthesis and biological evaluation of certain α, β-unsaturated ketones and their corresponding fused pyridines as antiviral and cytotoxic agents. J. Med. Chem., 43(15), 2915-2921
5. Lorand, T., Deli, J., Szabo, D., Foeldesi, A., and Zschunke, A. (1985) Potentially bioactive pyrimidine derivatives. III: 4-Aryl-8-arylidene-6-methyl-3, 4, 5, 6, 7, 8-hexahydropyrido [4, 3-d] pyrimidine-2 [1H]-ones and-2 (1H)-thiones. Pharmazie, 40(8), 536-539.
6. Elgemeie, G. E. H., Attia, A. M. E., and Alkabai, S. S. (2000) Nucleic acid components and their analogues: new synthesis of bicyclic thiopyrimidine nucleosides. Nucleos. Nucleot. Nucl, 19(4), 723-733.
7. Hammam, A. E. G., Sharaf, M. A., and El-Hafez, N. A. A. (2001) Synthesis and anti-cancer activity of pyridine and thiazolopyrimidine derivatives using 1-ethylpiperidone as a synthon. Indian J. Chem. Sec. B, 40(3), 213-221.
8. Zhu, Y., Huang, S., and Pan, Y. (2005) Highly chemoselective multicomponent biginelli‐type condensations of cycloalkanones, urea or thiourea and aldehydes. Eur. J. Org. Chem., 2005(11), 2354-2367.
9. Zhang, H., Zhou, Z., Yao, Z., Xu, F., and Shen, Q. (2009) Efficient synthesis of pyrimidinone derivatives by ytterbium chloride catalyzed Biginelli-type reaction under solvent-free conditions. Tetrahedron Lett., 50(14), 1622-1624.
10. Behbahani, F. K., and Farahani, M. (2011) Anhydrous FePO4 as a cost-effective and recyclable catalyst for tetrahydropyranylation and tetrahydrofuranylation of alcohols and phenols. Lett. Org. Chem., 8(6), 431-435.
11. Behbahani, F. K., and Yazdanparast, B. (2014) Iron (III) phosphate catalyzed synthesis of 1, 4-dihydropyridines. Arabian J. Chem., inpress. doi.org/10.1016/j.arabjc.2014.11.027
12. Hajipour, A. R., Ghayeb,Y., Sheikhan, N., and Ruoho, A. E. (2011) Brønsted acidic ionic liquid as an efficient and reusable catalyst for one-pot, three-component synthesis of pyrimidinone derivatives via Biginelli-type reaction under solvent-free conditions. Synthetic commun., 41(15), 2226-2233.
13. Kiyani, H., and Ghiasi, M. (2014). Potassium phthalimide: An efficient and green organocatalyst for the synthesis of 4-aryl-7-(arylmethylene)-3, 4, 6, 7-tetrahydro-1H-cyclopenta [d] pyrimidin-2 (5H)-ones/thiones under solvent-free conditions. Chin. Chem. Lett., 25(2), 313-316.
2. Kappe, C.O., Fabian, W.M.F., and 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(8), 2803-2816.
3. Rashad, A. E., Shamroukh, A.H., Yousif, N. M., Salama, M.A.; Ali, H.S.; Ali, M. M., Mahmoud, A.E., and El-Shahat, M. (2012) New pyrimidinone and fused pyrimidinone derivatives as potential anticancer chemotherapeutics. Archiv der Pharmazie, 345(9), 729-738.
4. El-Subbagh, H. I., Abu-Zaid, S. M., Mahran, M. A., Badria, F. A., and Al-Obaid, A. M. (2000) Synthesis and biological evaluation of certain α, β-unsaturated ketones and their corresponding fused pyridines as antiviral and cytotoxic agents. J. Med. Chem., 43(15), 2915-2921
5. Lorand, T., Deli, J., Szabo, D., Foeldesi, A., and Zschunke, A. (1985) Potentially bioactive pyrimidine derivatives. III: 4-Aryl-8-arylidene-6-methyl-3, 4, 5, 6, 7, 8-hexahydropyrido [4, 3-d] pyrimidine-2 [1H]-ones and-2 (1H)-thiones. Pharmazie, 40(8), 536-539.
6. Elgemeie, G. E. H., Attia, A. M. E., and Alkabai, S. S. (2000) Nucleic acid components and their analogues: new synthesis of bicyclic thiopyrimidine nucleosides. Nucleos. Nucleot. Nucl, 19(4), 723-733.
7. Hammam, A. E. G., Sharaf, M. A., and El-Hafez, N. A. A. (2001) Synthesis and anti-cancer activity of pyridine and thiazolopyrimidine derivatives using 1-ethylpiperidone as a synthon. Indian J. Chem. Sec. B, 40(3), 213-221.
8. Zhu, Y., Huang, S., and Pan, Y. (2005) Highly chemoselective multicomponent biginelli‐type condensations of cycloalkanones, urea or thiourea and aldehydes. Eur. J. Org. Chem., 2005(11), 2354-2367.
9. Zhang, H., Zhou, Z., Yao, Z., Xu, F., and Shen, Q. (2009) Efficient synthesis of pyrimidinone derivatives by ytterbium chloride catalyzed Biginelli-type reaction under solvent-free conditions. Tetrahedron Lett., 50(14), 1622-1624.
10. Behbahani, F. K., and Farahani, M. (2011) Anhydrous FePO4 as a cost-effective and recyclable catalyst for tetrahydropyranylation and tetrahydrofuranylation of alcohols and phenols. Lett. Org. Chem., 8(6), 431-435.
11. Behbahani, F. K., and Yazdanparast, B. (2014) Iron (III) phosphate catalyzed synthesis of 1, 4-dihydropyridines. Arabian J. Chem., inpress. doi.org/10.1016/j.arabjc.2014.11.027
12. Hajipour, A. R., Ghayeb,Y., Sheikhan, N., and Ruoho, A. E. (2011) Brønsted acidic ionic liquid as an efficient and reusable catalyst for one-pot, three-component synthesis of pyrimidinone derivatives via Biginelli-type reaction under solvent-free conditions. Synthetic commun., 41(15), 2226-2233.
13. Kiyani, H., and Ghiasi, M. (2014). Potassium phthalimide: An efficient and green organocatalyst for the synthesis of 4-aryl-7-(arylmethylene)-3, 4, 6, 7-tetrahydro-1H-cyclopenta [d] pyrimidin-2 (5H)-ones/thiones under solvent-free conditions. Chin. Chem. Lett., 25(2), 313-316.