Document Type : Original Research Article
Authors
Department of Chemistry, Payame Noor university, P. O. BOX 19395-3697, Tehran, Iran
Abstract
This work studies an efficient, one-pot pseudo multi-component synthesis of 3-amino-5-methyl-[1, 1'-biaryl]-2, 4-dicarbonitriles. This reaction performed under solvent free conditions in the presence of ZnFe2O4 magnetic nanoparticles. The ZnFe2O4 nanoparticles were prepared by an eco-friendly hydrothermal method
Graphical Abstract
![Synthesis of 3-amino-5-methyl-[1,1'-biaryl]-2,4-dicarbonitriles using ZnFe2O4 magnetic nanoparticles](javascript:loadModal('Synthesis of 3-amino-5-methyl-[1,1'-biaryl]-2,4-di ... ', 'data/ajgc/coversheet/431615956732.jpg'))
Keywords
[1]. Cui S.L., Lin X.F., Wang Y.G. J. Org. Chem., 2005, 70:2866
[2]. Kanis D.R., Ratner M.A., Marks T.J. Chem. Rev., 1994, 94:195
[3]. Long N.J. Angew. Chem., Int. Ed., 1995, 34:21
[4]. Carroll R.L., Gorman C.B. Angew. Chem., Int. Ed, 2002, 41:4378
[5]. Bendikov M., Wudl F., Perepichka D.F. Chem. Rev., 2004, 104:4891
[6]. Singh F.V., Vatsyayan R., Roy U., Goel A. Bioorg. Med. Chem. Lett., 2006, 16:2734
[7]. Rong L., Han H., Yang F., Yao H., Jiang H., Tu S. Synth. Commun., 2007, 37:3767
[8]. Adib M., Mohammadi B., Mahdavi M., Abbasi A., Kesheh M.R. Synlett, 2007, 2007:2497
[9]. Goel A., Singh F.V. Tetrahedron lett., 2005, 46:5585
[10]. Adib M., Mohammadi B., Ansari S., Bijanzadeh H.R., Zhu L.G. Synthesis, 2010, 2010:1526
[11]. Victory P., Borrell J.I., Vidal-Ferran A., Seoane C., Soto J.L. Tetrahedron lett., 1991, 32:5375
[12]. Yi C., Blum C., Liu S.X., Frei G., Neels A., Renaud P., Leutwyler S., Decurtins S. J. Org. Chem., 2008, 73:3596
[13]. Xue D., Li J., Zhang Z.T., Deng J.G. J. Org. Chem., 2007, 72:5443
[14]. Singh F.V., Kumar V., Kumar B., Goel A. Tetrahedron, 2007, 63:10971
[15]. Rong L., Han H., Jiang H., Shi D., Tu S. Synth. Commun., 2008, 38:1044
[16]. Ma’mani L., Heydari A., Sheykhan M. Appl. Catal., A, 2010, 384:122
[17]. Shylesh S., Schünemann V., Thiel W.R. Angew. Chem., Int. Ed, 2010, 49:3428
[18]. Jadhav S.V., Jinka K.M., Bajaj H.C. Catal. Today, 2012, 198:98
[19]. Singh A.S., Patil U.B., Nagarkar J.M. Catal. Commun., 2013, 35:11
[20]. Singh A.S., Shendage S.S., Nagarkar J.M. Tetrahedron Lett., 2013, 54:6319
[21]. Khorrami S., Gharib F., Mahmoudzadeh G., Sadat Sepehr S., Sadat Madani S., Naderfar N., Manie, SInt. J. Nano Dimens., 2011, 1:221
[22]. Kinnari P., Upadhyay R.V., Mehta R.V. J. Magn. Magn. Mater., 2002, 252:35
[23]. Zhu H., Gu X., Zuo D., Wang Z., Wang N., Yao K. Nanotechnology, 2008, 19:405503
[24]. Nakashima S., Fujita K., Tanaka K., Hirao K. J. Phys. Condens. Matter, 2004, 17:137
[25]. Cao S.W., Zhu Y.J., Cheng G.F., Huang Y.H. J. Hazard. Mater., 2009, 171:431
[26]. Xing Z., Ju Z., Yang J., Xu H., Qian Y. Nano Res., 2012, 5:477
[27]. Šepelák, V. In Annales de Chimie Science des Matériaux: Elsevier, 2002, 27:61
[28]. Viswanath I.K., Murthy Y., Tata K.R., Singh R. Int. J. Chem. Sci., 2013, 11:64
[29]. Mohammadi B., Rahmani M. Iran. Chem. Commun., 2016, 4:226
[30]. Mohammadi B., Shafieey M., Kazemi H. Iran. Chem. Commun., 2015, 3:302
[31]. Ghorbani M., Mohammadi B., Saraii M., Masoumi B., Abbasian M., Ramazani A., Slepokura K., Lis T. Org. Lett., 2016, 18:4759
[32]. Mohammadi B., Rezaei E., Moghadami F. Iran. Chem. Commun., 2018, 6:261
[33]. Laokul P., Amornkitbamrung V., Seraphin S., Maensiri S. Curr. Appl. Phys., 2011, 11:101
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