An air stable and efficient palladium catalyst for Suzuki-Miyaura cross coupling reaction at room temperature

Subject Areas : Iranian Journal of Catalysis

Raheleh Pourkaveh ¹ , Hirbod Karimi ²

1 - Laboratory of Organic Synthesis and Natural Products, Department of Chemistry, Sharif University of Technology, Azadi Street, PO Box 111559516 Tehran, Iran.
2 - Young Researchers and Elite Club, Shahreza Branch, Islamic Azad University, Shahreza, Iran.

Received: 2016-07-25 Accepted : 2016-10-21 Published : 2016-12-01

Keywords:

References:

[1] J.K. Stille, Angew. Chem. 98 (1986) 504-519.
[2] A. Talhami, L. Penn, N. Jaber, K. Hamza, J. Blum, Appl. Catal. A. 312 (2006) 115-119.
[3] A. Suzuki, J. Organomet. Chem. 576 (1999) 147-168.
[4] J. Sun, Y. Fu, G. He, X. Sun, X. Wang, Appl. Catal. B 165 (2015) 661-667.
[5] H. Ma, Z. Bao, G. Han, N. Yang, Y. Xu, Z. Yang, W. Cao, Y. Ma, Chin. J. Catal. 34 (2013) 578-584.
[6] D. Zhang, Q. Wang, Coord. Chem. Rev. 286 (2015) 1-16.
[7] Y. Hatanaka, T. Hiyama, Synlett. 1991 (1991) 845-853.
[8] A. Fodor, Z. Hell, L. Pirault-Roy, Appl. Catal. A. 484 (2014) 39-50.
[9] M.I. Burrueco, M. Mora, C. Jiménez-Sanchidrián, J.R. Ruiz, Appl. Catal. A. 485 (2014) 196-201.
[10] K. Niknam, M.S. Habibabad, A. Deris, F. Panahi, M. Reza Hormozi Nezhad, J. Iran. Chem. Soc. 10 (2013) 527-534.
[11] S. YaŞAr, I. ÖZdemir, B. ÇEtinkaya, Chin. J. Catal. 29 (2008) 185-190.
[12] D. Yuan, H. Zhang, Appl. Catal. A. 475 (2014) 249-255.
[13] B. Tamami, F.N. Dodeji, J. Iran. Chem. Soc. 9 (2012) 841-850.
[14] J. Lasri, T.C.O.M. Leod, A.J.L. Pombeiro, Appl. Catal. A. 397 (2011) 94-102.
[15] S. Ungureanu, H. Deleuze, O. Babot, M.F. Achard, C. Sanchez, M.I. Popa, R. Backov, Appl. Catal. A. 390 (2010) 51-58.
[16] M. Zhang, M. Jiang, C. Liang, Chin. J. Catal. 34 (2013) 2161-2166.
[17] Z. Peng, H. Fu, M. Ma, H. Chen, X. Li, Chin. J. Catal. 31 (2010) 1478-1482.
[18] B. Tamami, F. Farjadian, J. Iran. Chem. Soc. 8 (2011) S77-S88.
[19] G. Bringmann, S. Rüdenauer, T. Bruhn, L. Benson, R. Brun, Tetrahedron 64 (2008) 5563-5568.
[20] Y.Q. Fang, R. Karisch, M. Lautens, J. Org. Chem. 72 (2007) 1341-1346.
[21] J. Hassan, M. Sévignon, C. Gozzi, E. Schulz, M. Lemaire, Chem. Rev. 102 (2002) 1359-1469.
[22] L. Hu, K. Maurer, K.D. Moeller, Org. Lett. 11 (2009) 1273-1276.
[23] H. Mahdavi, P. Hashemi, J. Chin. Chem. Soc. 60 (2013) 425-436.
[24] J. Hsiao, C.M. Weng, F.E. Hong, J. Chin. Chem. Soc. 59 (2012) 733-742.
[25] A.S. Diez, M. Graziano-Mayer, G. Radivoy, M.A. Volpe, Appl. Catal. A. 482 (2014) 24-30.
[26] E. Mieczyńska, T. Borkowski, M. Cypryk, P. Pospiech, A.M. Trzeciak, Appl. Catal. A. 470 (2014) 24-30.
[27] F. Siga, H. Temel, M. Aydemir, Y.S. Ocak, S. Pasa, A. Baysal, Appl. Catal. A. 449 (2012) 172-182.
[28] J. Hsiao, C.M. Weng, F.E. Hong, J. Chin. Chem. Soc. 59 (2012) 161-169.
[29] N.T. Bui, T.B. Dang, H.V. Le, N.T.S. Phan, Chin. J. Catal. 32 (2011) 1667-1676.
[30] K. Bester, A. Bukowska, W. Bukowski, Appl. Catal. A. 443-444 (2012) 181-190.
[31] A. Hassine, S. Sebti, A. Solhy, M. Zahouily, C. Len, M.N. Hedhili, A. Fihri, Appl. Catal. A. 450 (2013) 13-18.
[32] A. Zapf, M. Beller, Topics Catal. 19 (2002) 101-109.
[33] L. Zhang, C. Feng, S. Gao, Z. Wang, C. Wang, Catal. Commun. 61 (2015) 21-25.
[34] M. Rosol, A. Moyano, J. Organomet. Chem. 690 (2005) 2291-2296.
[35] T. Jeffery, Tetrahedron 52 (1996) 10113-10130.
[36] A.R. Hajipour, R. Pourkaveh, H. Karimi, J. Organomet. Chem. 28 (2014) 879-883.
[37] N. Kataoka, Q. Shelby, J.P. Stambuli, J.F. Hartwig, The J. Org. Chem. 67 (2002) 5553-5566.
[38] A.S. Singh, R.S. Shelkar, J.M. Nagarkar, Catal. Lett. 145 (2015) 723-730.
[39] T. Rosner, J. Le Bars, A. Pfaltz, D.G. Blackmond, J. Am. Chem. Soc. 123 (2001) 1848-1855.
[40] M.R. Eberhard, Org. Lett. 6 (2004) 2125-2128.
[41] A.S. Singh, R.S. Shelkar, J.M. Nagarkar. Catal. Lett. 145 (2015) 723-730.
[42] D.M. Pore, D.S. Gaikwad, J.D. Patil. Monatsh. Chem. 144 (2013) 1355-1361.
[43] J. Liu, Y.-Q. Li, W.-J. Zheng. Monatsh. Chem. 140 (2009) 1425-1429.