تعداد نشریات | 418 |
تعداد شمارهها | 10,005 |
تعداد مقالات | 83,618 |
تعداد مشاهده مقاله | 78,303,071 |
تعداد دریافت فایل اصل مقاله | 55,356,828 |
Polymer-supported basic ionic liquid as an efficient heterogeneous catalyst system for straightforward synthesis of flavanones | ||
Iranian Journal of Catalysis | ||
مقاله 11، دوره 6، شماره 2، شهریور 2016، صفحه 167-172 اصل مقاله (1.04 M) | ||
نوع مقاله: Articles | ||
نویسندگان | ||
Soheil Sayyahi* 1؛ Somayeh Heidari2 | ||
1Department of Chemistry, Mahshahr Branch, Islamic Azad University, Mahshahr, Iran. | ||
2Department of Chemistry, Omidieh Branch, Islamic Azad University, Omidieh, Iran. | ||
چکیده | ||
Aromatic aldehydes are efficiently condensed with 2'-hydroxyacetophenone by polymer-supported basic ionic liquid as an excellent heterogeneous catalyst utilizing the Claisen–Schmidt reaction. Microwave irradiation has been employed, providing flavanone in good yield and short reaction time. | ||
کلیدواژهها | ||
Polymer-supported catalyst؛ Immobilization؛ Basic ionic liquid؛ Flavanone | ||
مراجع | ||
[1] H. Olivier-Bourbigou, L. Magna, D. Morvan, Appl. Catal. A 373 (2010) 1-56. [2] D.D. Patel, J.M. Lee, Chem. Rec. 12 (2012) 329-355. [3] A.R. Hajipour, F. Rafiee, J. Iran. Chem. Soc. 6 (2009) 647-678. [4] S. Abello, F. Medina, X. Rodriguez, Y. Cesteros, P. Salagre, J.E. Sueiras, D. Tichit, B. Coq, Chem. Commun. (2004) 1096-1097. [5] H. Li, P.S. Bhadury, B. Song, S. Yang, RSC Adv. 2 (2012) 12525-12551. [6] C.P. Mehnert, Chem- Eur. J. 11 (2005) 50-56. [7] C. Yuan, Z. Huang, J. Chen, Catal. Commun. 24 (2012) 56-60. [8] D.W. Kim, D.J. Hong, K.S. Jang, D.Y. Chi, Adv. Synth. Catal. 348 (2006) 1719-1727. [9] A.E. Nibbs, K.A. Scheidt, Eur. J. Org. Chem. 2012 (2012)449-462. [10] W. Ren, Z. Qiao, H. Wang, L. Zhu, L. Zhang, Med. Res. Rev. 23 (2003) 519-534. [11] H. Yoon, T.W. Kim, S.Y. Shin, M.J. Park, Y. Yong, D.W. Kim, T. Islam, Y.H. Lee, K.-Y. Jung, Y. Lim, Bioorg. Med. Chem. Lett. 23 (2013)232-238. [12] M. Cabrera, M. Simoens, G. Falchi, M.L. Lavaggi, O.E. Piro, E.E. Castellano, A. Vidal, A. Azqueta, A. Monge, A.L. de Ceráin, G. Sagrera, G. Seoane, H. Cerecetto, M. González, Bioorg. Med. Chem. 15 (2007) 3356-3367. [13] N. Anand, P. Singh, A. Sharma, S. Tiwari, V. Singh, D.K. Singh, K.K. Srivastava, B.N. Singh, R.P. Tripathi, Bioorg. Med. Chem. 20 (2012) 5150-5163. [14] M. Safavi, N. Esmati, S.K. Ardestani, S. Emami, S. Ajdari, J. Davoodi, A. Shafiee, A. Foroumadi, Eur. J. Med. Chem. 58 (2012) 573-580. [15] D. French, P. Schifano, J. Cortés-Concepción, S. Hargrove-Leak, Catal. Commun. 12(2010) 92-94. [16] J. A. Cortes-Concepcion, F. Patcas, M.D. Amiridis, Appl. Catal. A 386 (2010) 1-8. [17] X. Wang, Y.-H. Tseng, J.C.C. Chan, S. Cheng, J. Catal. 233 (2005) 266-275. [18] V. Kavala, C. Lin, C.-W. Kuo, H. Fang, C.-F. Yao, Tetrahedron 68 (2012) 1321-1329. [19] S. Chandrasekhar, K. Vijeender, K.V. Reddy, Tetrahedron Lett. 46 (2005) 6991-6993. [20] R. Mondal, A.D. Gupta, A.K. Mallik, Tetrahedron Lett. 52 (2011)5020-5024. [21] R. Sakirolla, M. Yaeghoobi, N. Abd. Rahman, Monatsh. Chem. 143 (2012) 797-800. [22] A. R. Kiasat, S. Sayyahi, Mol. Diversity 14 (2010) 155-158. [23] A.R. Kiasat, S. Sayyahi, Catal. Commun. 11 (2010) 484-486. [24] S. Sayyahi, H.M. Rezaee, F.S. Khalfabadi, M. Gorjizadeh, J. Chem. Res. 36 (2012) 396-397. [25] S. Sayyahi, J. Saghanezhad, Chin. Chem. Lett. 22 (2011) 300-302. [26] A. Fauvel, H. Deleuze, Y. Landais, Eur. J. Org. Chem. 2005 (2005) 3900-3910. [27] B.-H. Jun, J.-H. Kim, J. Park, H. Kang, S.-H. Lee, Y.-S. Lee, Synlett (2008) 2313-2316. [28] N. Galaffu, G. Sechi, M. Bradley, Mol. Diversity 9 (2005) 263-275. [29] D. Kumar, G. Patel, A. Kumar, R. K. Roy, J. Heterocycl. Chem. 46 (2009) 791-795. [30] B.M. Choudary, K.V.S. Ranganath, J. Yadav, M.L. Kantam, Tetrahedron Lett. 46 (2005) 1369-1371. [31] L.B. Kunde, S.M. Gade, V.S. Kalyani, S.P. Gupte, Catal. Commun. 10 (2009) 1881-1888. | ||
آمار تعداد مشاهده مقاله: 837 تعداد دریافت فایل اصل مقاله: 898 |