Shaterian et al.
ACKNOWLEDGEMENTS
Tilestam, Tetrahedron Lett. 43 (2002) 593.
[16] a) S. Sarshar, D. Siev, A.M.M. Mjalli, Tetrahedron
Lett. 37 (1996) 835; b) D.E. Frantz, L. Morency, A.
Soheili, J.A. Murry, E.J.J. Grabowski, R.D. Tillyer,
Org. Lett. 6 (2004) 843.
We are thankful to Sistan and Baluchestan University
Research Council for the partial support of this research.
REFERENCES
[17] M.V. Chary, N.C. Keerthysri, S.V.N. Vupallapati, N.
Lingaiahi, S. Kantevari, Catal. Commun. 9 (2008)
2013.
[18] L.M. Wang, Y.H. Wang, H. Tian, Y.F. Yao, J.H. Shao,
B. Liu, J. Fluorine Chem.127 (2006) 1570.
[19] S.A. Siddiqui, U.C. Narkhede, S.S. Palimkar, T. Daniel,
R.J. Lahoti, K.V. Srinivasan, Tetrahedron 61 (2005)
3539.
[20] T. Heinze, T. Liebert, Prog. Polym. Sci. 26 (2001)
1689.
[21] D.M. White, J. Sonnenberg. J. Org. Chem. 29 (1964)
1926.
[1]
[2]
[3]
M.M. Heravi, S. Sadjadi, J. Iran. Chem. Soc. 6 (2009)
1.
J. Zhu, H. Bienayme, Multicomponent Reaction, Wily-
VCH, France, 2005.
a) K. Niknam, A. Fatehi-Raviz, J. Iran. Chem. Soc. 4
(2007) 438; b) B. Sadeghi, B.B.F. Mirjalili, S. Bidaki,
M. Ghasemkhani, J. Iran. Chem. Soc. 8 (2011) 648.
R. Breslow, Acc. Chem. Res. 28 (1995) 146.
H.V.D. Bossche, G. Willemsens, W. Cools, P.
Marichal, W. Lauwers, Bio. Chem. Soc. Trans. 11
(1983) 665.
[4]
[5]
[22] J.F. Zhou, Y.Z. Song, Y.L. Yang, Y.L. Zhu, Synth.
Commun. 35 (2005) 1369.
[23] S. Samai, G.C. Nandi, M.S. Singh, Tetrahedron 65
(2009) 10155.
[6]
J. Freedman, J. Loscalzo, New Therapeutic Agent in
Thrombosis and Thrombolysis, 3th ed., Taylor and
Francis, 2009.
[7]
[8]
[9]
A.R. Hajipour, F. Rafiee, J. Iran. Chem. Soc. 6 (2009)
647.
H. Shaterian, A.R. Oveisi. J. Iran. Chem. Soc. 8 (2011)
545.
M. Freemantle, Introduction to Ionic Liquids, Royal
Society of Chemistry, Cambridg CB4 OWF, UK, 2009.
[24] M. Frank, DE Patent 4,320,802 (1995).
[25] D.A. Evans, K.M. Lundy, J. Am. Chem. Soc. 114
(1992) 1495.
[26] A. Hasaninejad, A. Zare, M. Shokouhy, J. Ameri Rad,
J. Comb. Chem. 12 (2010) 844.
[27] K.F. Shelke, S.B. Sapkal, S.S. Sonar, B. Korean. J. Am.
Chem. Soc. 30 (2009) 5.
[28] H. Zang, Q. Su, Mo. Yingming, B.W. Cheng, S. Jun,
Ultrason. Sonochem. 17 (2010) 749.
[10] P. Wasserscheid, T. Welton, Ionic Liquids in Synthesis,
Wiley-VCH, Germany, 2008.
[11] R.A. Sheldon, I. Arends, U. Hanefeld, Green Chemistry
and Catalyst, Delft University of Tecnology, The
Netherlands, Wiley-VCH, 2007.
[29] R.P. Kale, G.R. Jadhav, M.U. Shaikh, Tetrahedron Lett.
50 (2009) 1780.
[12] a) H.R. Shaterian, H. Yarahmadi, M. Ghashang,
Tetrahedron 64 (2008) 1263; b) H.R. Shaterian, M.
Honarmand, A.R. Oveisi, Monatsh. Chem. 141 (2010)
557; c) H.R. Shaterian, A.R. Oveisi, Chin. J. Chem. 27
(2009) 2418; d) H.R. Shaterian, A. Hossienian, M.
Ghashang, Turk. J. Chem. 2 (2009) 233.
[30] A. Mohammadi, M. Mivechi, H. Kefayati, Monatsh.
Chem. 139 (2008) 935.
[31] D.E. Frantz, L. Morency, A. Soheilli, J.A. Murrry,
E.J.J. Grabowski, R.D. Tillyer, Org. Lett. 6 (2004) 843.
[32] M.M. Heravi, F. Drikvand, F.F. Bamoharram, J. Mol.
Catal. 263 (2007) 112.
[13] C. Cole, J.L. Jensen, I. Nati, K.L.T. Tran, K.J. Weaver,
D. Forbes, J. Am. Chem. Soc. 124 (2002) 5962.
[14] J. Liu, J. Chem. J. Zhao, Y. Zhao, L. Li, H. Zhang,
Synthesis (2003) 2661.
[33] A. Karimi, R. Alimohammadi, Z. Azizian, J.
Mohammadi, A.A. Mohammadizadeh, Catal. Commun.
7 (2006) 728.
[34] S. Kantevari, S.V.N. Vuppalapati, D.O. Biradar, L.
Nagarapu, J. Mol. Catal. 266 (2007) 109.
[15] H. Weinmann, M. Harre, K. Koeing, E. Merten, U.
1133