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Melamine trisulfonic acid as a highly efficient catalyst for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes under solvent-free conditions | ||
Iranian chemical communication | ||
مقاله 1، دوره 2، Issue 1, pp. 1-81, Serial No. 2، فروردین 2014، صفحه 1-17 اصل مقاله (308.93 K) | ||
نوع مقاله: Original Research Article | ||
نویسندگان | ||
Abdolkarim Zare* ؛ Fatemeh Monfared | ||
Department of Chemistry, Payame Noor University, PO BOX 19395-4697 Tehran, Iran | ||
چکیده | ||
Melamine trisulfonic acid (MTSA) is utilized as a highly efficient catalyst for the solvent-free condensation reaction of 2-naphthol (2 eq.) with arylaldehydes (1 eq.) under conventional thermal as well as microwave conditions to give the d | ||
کلیدواژهها | ||
14-Aryl-14H-dibenzo[a؛ j]xanthene؛ melamine trisulfonic acid (MTSA)؛ 2-naphtol؛ arylaldehyde؛ solvent-free؛ microwave | ||
اصل مقاله | ||
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مراجع | ||
[1] T. Hideo, Chem. Abstr., 1981, 95, 80922b, Jpn. TokkyoKoho JP 56005480, 1981. [2] R.W. Lambert, J.A. Martin, J.H. Merrett, K.E.B. Parker, G.J. Thomas, PCT Int. Appl. WO9706178, 1997. [3] J.P. Poupelin, G.S. Ruf, O.F. Blanpin, G. Narcisse, G.U. Ernouf, R. Lacroix, Eur. J. Med. Chem., 1978, 13, 67-71. [4] R.M. Ion, D. Frackowiak, A. Planner, K. Wiktorowicz, Acta Biochem. Pol., 1998, 45, 833-845. [5] S.M. Menchen, S.C. Benson, J.Y.L. Lam, W. Zhen, D. Sun, B.B. Rosenblum, S.H. Khan, M. Taing, U.S. Patent 6, 2003, 583, 168. [6] A. Bekaert, J. Andrieux, M. Plat, Tetrahedron Lett., 1992, 33, 2805-2806. [7] S. Chatterjee, M. Iqbal, J.C. Kauer, J.P. Mallamo, S. Senadhi, S. Mallya, D. Bozyczko-Coyne, R. Siman, Bioorg. Med. Chem. Lett., 1996, 6, 1619-1622. [8] A. Naya, M. Ishikawa, K. Matsuda, K. Ohwaki, T. Saeki, K. Noguchi, N. Ohtake, Bioorg. Med. Chem., 2003, 11, 875-884. [9] I.Mohammadpoor-Baltork, M. Moghadam, V. Mirkhani, S. Tangestaninejad, H.R. Tavakoli, Chin. Chem. Lett., 2011, 22, 9-12. [10] G. Karthikeyan, A. Pandurangan, J. Mol. Catal. A: Chem., 2009, 311,36-45. [11] P.S. Kumar, B.S. Kumar, B. Rajitha, P.N. Reddy, N. Sreenivasulu, Y.T. Reddy, ARKIVOC,2006, xii, 46-50. [12] M. Dabiri, M. Baghbanzadeh, M.S. Nikcheh, E. Arzroomchilar, Bioorg. Med. Chem.Lett., 2008, 18, 436-438. [13] B.F. Mirjalili, A. Bamoniri, A. Akbari, N. Taghavinia, J. Iran. Chem. Soc.,2011, 8, 129-134. [14] M.A. Bigdeli, M.M. Heravi, G.H. Mahdavinia, Catal. Commun.,2007, 8, 1595-1598. [15] A. Zare, A.R. Moosavi-Zare, M. Merajoddin, M.A. Zolfigol, T. Hekmat-Zadeh, A. Hasaninejad, A. Khazaei, M. Mokhlesi, V. Khakyzadeh, F. Derakhshan-Panah, M.H. Beyzavi, E. Rostami, A. Argoon, R. Roohandeh, J. Mol. Liq.,2012, 167, 69-77. [16] M. Hong, C. Cai, J. Fluorine Chem.,2009, 130, 989-992. [17] A.K. Bhattacharya, K.C. Rana, M. Mujahid, I. Sehar, A.K. Saxena, Bioorg. Med. Chem. Lett.,2009, 19, 5590-5593. [18] G.I. Shakibaei, P. Mirzaei, A. Bazgir, Appl. Catal. A: Gen.,2007, 325, 188-192. [19] W. Su, D. Yang, C. Jin, B. Zhang, Tetrahedron Lett.,2008, 49, 3391-3394. [20] A.R. Momeni, M. Sadeghi, Appl. Catal. A: Gen.,2009, 357, 100-105. [21] A. Khalafi-Nezhad, A. Parhami, R. Bargebid, S. Molazade, A. Zare, H. Foroughi, Mol. Divers.,2011, 15, 373-381. [22] A.R. Moosavi-Zare, M.A. Zolfigol, M. Zarei, A. Zare, V. Khakyzadeh, A. Hasaninejad, Appl. Catal. A: Gen.,2013, 467, 61-68. [23] A.R. Moosavi-Zare, M.A. Zolfigol, M. Zarei, A. Zare, V. Khakyzadeh, J. Mol. Liq., 2013, 186, 63-69. [24] A.R. Kiasat, M. Fallah-Mehrjardi, Synth. Commun., 2010, 40, 1551-1558. [25] F. Shirini, M.A. Zolfigol, J. Albadi, J. Iran. Chem. Soc., 2010, 7,895-899. [26] F. Shirini, M.A. Zolfigol, J. Albadi, Chin. Chem. Lett., 2011, 22, 318-321. [27] F. Shirini, M.A. Zolfigol, A.-R. Aliakbar, J. Albadi, Synth. Commun., 2010, 40, 1022-1028. [28] F. Shirini, J. Albadi, Bull. Korean Chem. Soc.,2010, 31,1119-1120. [29] K. Tanaka, Solvent-free Organic Synthesis, Wiley- VCH, GmbH and KGaA, Weinheim, 2004. [30] A. Khazaei, M. A. Zolfigol, A.R. Moosavi-Zare, A. Zare, M. Khojasteh, Z. Asgari, V. Khakyzadeh, A. Khalafi- Nezhad, Catal. Commun.,2012, 20, 54-57. [31] M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare, A. Zare, V. Khakyzadeh, Appl. Catal. A: Gen.,2011, 400, 70-81. [32] A. Loupy, Microwave in Organic Synthesis, Wiley- VCH, Weinheim, 2006. [33] A. Zare, A. Hasaninejad, A. Salimi Beni, A.R. Moosavi-Zare, M. Merajoddin, E. Kamali, M. Akbari-Seddigh, Z. Parsaee, Sci. Iran. C, 2011, 18, 433-438. [34] B. Rajitha, B.S. Kumar, Y.T. Reddy, P.N. Reddy, N. Sreenivasulu, Tetrahedron Lett., 2005, 46, 8691-8693. [35] T.S. Jin, J.S. Zhang, J.C. Xiao, A.Q. Wang, T.S. Li, Synlett, 2004, 866-870. [36] A. Zare, M. Merajoddin, F. Abi, A.R. Moosavi-Zare, M. Mokhlesi, M.A. Zolfigol, Z. Asgari, V. Khakyzadeh, A. Hasaninejad, A. Khalafi-Nezhad, A. Parhami, J. Chin. Chem., Soc.,2012, 59, 860-865. [37] M.A. Zolfigol, A.R. Moosavi-Zare, P. Arghavani-Hadi, A. Zare, V. Khakyzadeh, G. Darvishi, RSC Adv., 2012, 2, 3618-3620. | ||
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