Introduction of two efficient catalysts for the synthesis of 1,8-dioxo-octahydroxanthene derivatives in the absence of solvent
محورهای موضوعی : Iranian Journal of CatalysisFarhad Shirini 1 , Gholam Hossein Imanzadeh 2 , Masoumeh Abedini 3 , Maryam Akberi Dokhte-Ghaziani 4 , Mohaddeshes Safarpoor Langroodi 5 , Parisa Ghods Ghasemabadi 6
1 - Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.
2 - Department of Chemistry, College of Science, Mohaghegh-Ardabili University, Ardabil, I.R. Iran.
3 - Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.
4 - Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.
5 - Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.
6 - Department of Chemistry, College of Science, Mohaghegh-Ardabili University, Ardabil, I.R. Iran.
Department of Chemistry, College of Science, University of Guilan, Rasht, zip code 41335, I.R. Iran.
کلید واژه: 1, Aldehydes, 5-dimethylhydantoin, Cyclic 1, 3-dicarbonyl compounds, Solvent-free conditions, 8-Dioxo-octahydroxanthenes, 3-Dibromo-5, Benzyltriphenylphosphoniumtribromide,
چکیده مقاله :
1,3-Dibromo-5,5-dimethylhydantoin (DBH) and benzyltriphenylphosphoniumtribromide (BTPTB) were used as efficient catalysts for the promotion of the synthesis of 1,8-dioxo-octahydroxanthene derivatives (DOXOs) via a one-pot three component condensation of aldehydes and cyclic 1,3-dicarbonyl compounds in the absence of solvent.
[1] A. Shaabani, A. Maleki, A.H. Rezayan, A. Sarvary, Mol. Div. 15 (2011) 41-68.
[2] Y.M. Ren, C. Cai, Monatsch. Chem. 140 (2009) 49-52.
[3] S. Bondock, H. El-Azap, E.E.M. Kandeel, M.A. Metwally, Monatsch. Chem. 139 (2008) 1329-1335.
[4] L. Liu, L.Y. Ji, Y.Y. Wei, Monatsch. Chem. 139 (2008) 901-903.
[5] T. Hideu, .JpnTokkyoKoho JP 56005480; 1981 (Chem. Abstr. 1981, 95. 80922b).
[6] R.W. Lamberk, J.A. Marti, J.H. Merrett, K.E.B. Parkers, G. Thomas, J. PCT Int. Appl. WO 9706178, 1997 (Chem. Abstr. 1997, 126. P212377y).
[7] J.P. Poupelin, G. Saint-Rut, O. Fussard-Blanpin, G. Narcisse, G. Uchida-Ernouf, R. Lakroix, Eur. J. Med. Chem. 13 (1978) 67-71.
[8] R.M. Ion, A. Planner, K. Wiktorowicz, D. Frackowiak, Acta. Biochem. Pol. 45 (1998) 833-845.
[9] B. Das, P. Thirupathi, K.R. Reddy, B. Ravikanth, L. Nagarapu, Catal. Commun. 8 (2007) 535-538
[10] M. Seyyedhamzeh, P. Mirzaei, A. Bazgir, Dyes & Pig. 76 (2008) 836-839.
[11] B. Das, P. Thirupathi, I. Mehender, V.S. Reddy, Y.K. Rao, J. Mol. Catal. A: Chem. 247 (2006) 233-239.
[12] G. ImaniShakibaei, P. Mirzaei, A. Bazgir, Appl. Catal. A: General 325 (2007) 188-192.
[13] M.A. Bigdeli, F. Nemati, G.H. Mahdavinia, H. Doostmohammadi, Chin. Chem. Lett. 20 (2009) 1275-1278.
[14] M. Dabiri, M. Baghbanzadeh, E. Arzroomchilar, Catal. Commun. 9 (2008) 939-942.
[15] K. Venkatesan, S.S. Pujari, R.J. Lahoti, K.V. Srinivasan, Ultrason. Sonochem. 15 (2008) 548-553.
[16] T.S. Jin, J.S. Zhang, J.C. Xiao, A.Q. Wang, T.S. Li, Synlett (2004) 866-870.
[17] G. Song, B. Wang, H. Luo, L. Yang, Catal. Commun. 8 (2007) 673-676.
[18] S. Kantevari, R. Bantu, L. Nagarapu, J. Mol. Catal. A: Chem. 269 (2007) 53-57.
[19] K. Niknam, M. Damya, J. Chin. Chem. Soc. 56 (2009) 659-665.
[20] F. Shirini, M.A. Zolfigol, M. Paktinat, M. Synthesis (2006) 4252-4256.
[21] F. Shirini, G.H. Imanzadeh, S.A.R. Mousazadeh, I. Mohammadpoor-Baltork, M. Abedini, Chin. Chem. Lett. 21 (2010) 1187-1190.
[22] F. Shirini, G.H. Imanzadeh, A.R. Mousazadeh, I. Mohammadpoor-Baltork, A.R. Aliakbar, M. Abedini, Phosphorous, Sulfur, Silicon 185 (2010) 641-646.
[23] F. Shirini, M. SafarpoorLangroodi, M. Abedini, Chin. Chem. Lett. 21 (2010) 1342-1345.
[24] F. Shirini, G. H. Imanzadeh, A.R. Mousazadeh, A.R Aliakbar, Phosphorous, Sulfur, Silicon 185 (2010) 1640-1644.
[25] D. Fang, K. Gong, Z.L. Liu, Catal. Lett. 127 (2009) 291-295.
[26] L. Li-Bin, J. Tong-Shou, H. Li-Sha, L. Meng, Q. Na, L. Tong-Shuang, Eur. J. Chem. 3 (2006) 117-121.
[27] H.Y. Lu, J.J. Li, JZ.H. Zhang, Appl. Organo. Metal. Chem. 23 (2009) 165-169.
[28] M.T. Maghsoodlou, S.M. Habibi-Khorassani, Z. Shahkarami, N. Maleki, M. Rostamizadeh, Chin. Chem. Lett. 21 (2010) 686-689.
[29] S. Rostamizadeh, A.M. Amani, G.H. Mahdavinia, G. Amiri, H. Sepehrian, Ultrason. Sonochem.17 (2010) 306-309.
[30] M. Bigdeli, Chin. Chem. Lett. 21 (2010) 1180-1182.