Palladium Schiff-base complex loaded SBA-15 as a novel nanocatalyst for the synthesis of 2,3-disubstituted quinoxalines and pyridopyrazine derivatives

Microporous and Mesoporous Materials

Volumn 169, Issue , 2013, Pages 67-74

  Bardajee, Ghasem Rezanejade ^a   Malakooti, Reihaneh ^b   Abtin, Ibrahim ^a   Atashin, Hassan ^b  

^a PAYAME NOOR UNIVERSITY   (Iran)

^b UNIVERSITY OF BIRJAND   (Iran)

Author keywords

Heterogeneous catalysis; Pd(II) complex; Pyridopyrazines; Quinoxalines; SBA 15

Indexed keywords

AROMATIC COMPOUNDS; COMPLEXATION; GAS ADSORPTION; HIGH RESOLUTION TRANSMISSION ELECTRON MICROSCOPY; NANOCATALYSTS; X RAY DIFFRACTION;

ATOMIC ABSORPTION; NITROGEN ADSORPTION; POWDER X RAY DIFFRACTION; PYRIDO[2 ,3-B]PYRAZINE; SCHIFF BASE COMPLEXES; SCHIFF-BASE LIGANDS; SUPPORTED PALLADIUM CATALYSTS; TEXTURAL PROPERTIES;

PALLADIUM COMPOUNDS;

EID: 84880237064     PISSN: 13871811     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.micromeso.2012.10.020     Document Type: Article

References (61)

1. Meynen, V., Cool, P., Vansant, E.F., Microporous Mesoporous Mater. 125 (2009), 170–223.
2. Taguchi, A., Schuth, F., Microporous Mesoporous Mater. 77 (2005), 1–45.
3. Yang, Q., Ma, S., Li, J., Xiao, F., Xiong, H., Chem. Commun., 2006, 2495–2497.
4. Zhang, J., Zhao, G.F., Popovic, Z., Lu, Y., Liu, Y., Mater. Res. Bull. 45 (2010), 1648–1653.
5. Blanco, B., Mehdi, A., Moreno-Manas, M., Pleixats, R., Reye, C., Tetrahedron Lett. 45 (2004), 8789–8791.
6. Crudden, C.M., Sateesh, M., Lewis, R., J. Am. Chem. Soc. 127 (2005), 10045–10050.
7. Richardson, J.M., Jones, C.W., J. Catal. 251 (2007), 80–93.
8. Webb, J.D., MacQuarrie, S., McEleney, K., Crudden, C.M., J. Catal. 252 (2007), 97–109.
9. karimi, B., Abedi, S., Clark, J.H., Budarin, V., Angew. Chem. Int. Ed. 45 (2006), 4776–4779.
10. Sayah, R., Glegoła, K., Framery, E., Dufaud, V., Adv. Synth. Catal. 349 (2007), 373–381.
11. Demel, J., Park, S.E., Cejka, J., Stepnicka, P., J. Mol. Catal. A: Chem. 302 (2009), 28–35.
12. Karimi, B., Zamani, A., Abedia, S., Clark, J.H., Green Chem. 11 (2009), 109–119.
13. Batail, N., Bendjeriou, A., Djakovitch, L., Dufaud, V., Appl. Catal. A 388 (2010), 179–187.
14. Demel, J., Cejka, J., Stepnicka, P., J. Mol. Catal. A: Chem. 329 (2010), 13–20.
15. Genelot, M., Dufaud, V., Djakovitch, L., Tetrahedron 67 (2011), 976–981.
16. Yadav, J.S., Reddy, B.V.S., Premalatha, K., Kattela, S., Synthesis, 2008, 3787–3792.
17. He, W., Meyers, M.R., Hanney, B., Sapada, A., Blider, G., Galzeinski, H., Amin, D., Needle, S., Page, K., Jayyosi, Z., Perrone, H., Bioorg. Med. Chem. Lett. 13 (2003), 3097–3100.
18. Sakata, G., Makino, K., Kuraswa, Y., Heterocycles 27 (1988), 2481–2515.
19. Brown, D.J., Taylor, E.C., Wipf, P., (eds.) The Chemistry of Heterocyclic Compounds, vol. 61, 2004, John Wiley & Sons, New Jersey.
20. Bhosale, R.S., Sarda, S.R., Andhapure, S.S., Jadhav, W.N., Bhusare, S.R., Pawar, R.P., Tetrahedron Lett. 46 (2005), 7183–7186.
21. More, S.V., Sastry, M.N.V., Wang, C., Yao, C.F., Tetrahedron Lett. 46 (2005), 6345–6348.
22. Huang, T.K., Wang, R., Shi, L., Lu, X.X., Catal. Commun. 9 (2008), 1143–1147.
23. Raw, S.A., Wilfred, C.D., Taylor, R.J.K., Org. Biomol. Chem. 2 (2004), 788–796.
24. Kim, S.Y., Park, K.H., Chung, Y.K., Chem. Commun., 2005, 1321–1323.
25. Robinson, R.S., Taylor, R.J.K., Synlett, 2005, 1003–1005.
26. Cho, C.S., Renb, W.X., Shim, S.C., Tetrahedron Lett. 48 (2007), 4665–4667.
27. Singh, S.K., Gupta, P., Duggineni, S., Kundu, B., Synlett, 2003, 2147–2150.
28. Antoniotti, S., Dunach, E., Tetrahedron Lett. 43 (2002), 3971–3973.
29. Das, B., Lu, K.V., Suneel, K., Majhi, A., Tetrahedron Lett. 48 (2007), 5371–5374.
30. Barluenga, J., Aznar, F., Liz, R., Cabal, M.P., Synthesis, 1985, 313–314.
31. Raw, S.A., Wilfred, C.D., Taylor, R.J.K., Chem. Commun., 2003, 2286–2287.
32. Cohen, Y., Meyer, A.Y., Rabinovitz, M., J. Am. Chem. Soc., 1986, 7039–7044.
33. Xekoukoulotakis, N.P., Hadjiantoniou, M., Maroulis, A.J., Tetrahedron Lett. 41 (2000), 10299–10302.
34. More, S.V., Sastry, M.N.V., Yao, C.F., Green Chem. 8 (2006), 91–95.
35. Zhao, Z., Wisnoski, D.D., Wolkenberg, S.E., Leister, W.H., Wang, Y., Lindsley, C.W., Tetrahedron Lett. 45 (2004), 4873–4876.
36. Goswami, S., Adak, A.K., Tetrahedron Lett. 46 (2005), 221–224.
37. Mohsenzadesh, F., Aghapoor, K., Darabai, H.R., J. Braz. Chem. Soc. 18 (2007), 297–304.
38. Cho, C.S., Oh, S.G., J. Mol. Catal. A: Chem. 276 (2007), 205–210.
39. Popp, F.D., J. Heterocycl. Chem. 9 (1972), 1399–1401.
40. Takekuma, S.I., Katayama, S., Takekuma, H., Chem. Lett., 2000, 614–615.
41. Sarkis, G.Y., Al-Badri, H.T., J. Heterocycl. Chem. 17 (1980), 813–815.
42. Chisem, I.C., Rafelt, J., Shieh, M.T., Chisem, J., Clark, J.H., Jachuck, R., Macquarrie, D., Ramshaw, C., Scott, K., Chem. Commun., 1998, 1949–1950.
43. Zhao, D., Feng, J., Huo, Q., Melosh, N., Fredrickson, G.H., Chmelka, B., Stucky, G.D., Science 279 (1998), 548–552.
44. Hou, J.T., Liu, Y.H., Zhang, Z.H., J. Heterocycl. Chem. 47 (2010), 703–706.
45. Li, J., Jiang, D.N., Chen, J.X., Liu, M.C., Ding, J.C., Wu, H.Y., J. Heterocycl. Chem. 48 (2011), 403–406.
46. Naskar, J.P., Chowdhury, S., Drew, M.G.B., Datta, D., New J. Chem. 26 (2002), 170–175.
47. Aghapoor, K., Darabi, H.R., Mohsenzadeh, F., Balavar, Y., Daneshyar, H., Transition Met. Chem. 35 (2010), 49–53.
48. Alinezhad, H., Tajbakhsh, M., Salehian, F., Biparva, P., Bull. Korean Chem. Soc. 32 (2011), 3720–3726.
49. Lü, H.Y., Yang, S.H., Deng, J., Zhang, Z.H., Aust. J. Chem. 63 (2010), 1290–1296.
50. Kaye, I.A., J. Med. Chem. 7 (1964), 240–241.
51. Antoine, M., Czech, M., Gerlach, M., Günther, E., Schuster, T., Marchand, P., Synthesis, 2011, 794–806.
52. Koenigs, E., Bueren, H., Jung, G., Chem. Ber. 69 (1936), 2690–2692.
53. Buu-Hoï, N.P., Saint-Ruf, G., Arcos, J.C., Bull. Soc. Chim. Fr., 1969, 838–842.
54. Appel, R., Volz, P., Chem. Ber. 108 (1975), 623–628.
55. Mohammadi, K., Hasaninejad, A., Niad, M., Najmi, M., J. Porphyrins Phthalocyanines, 2010, 1052–1058.
56. Rothkopf, H.W., Weohrle, D., Meuller, R., Kossmehl, G., Chem. Ber. 108 (1975), 875–882.
57. Jana, S., Dutta, B., Bera, R., Koner, S., Langmuir 23 (2007), 2492–2496.
58. Wang, X., Wu, G., Wei, W., Sun, Y., Catal. Lett. 136 (2010), 96–105.
59. Lim, M.H., Stein, A., Chem. Mater. 11 (1999), 3285–3295.
60. Zhang, W.H., Lu, X.B., Xiu, J.H., Hua, Z.L., Zhang, L.X., Robertson, M., Shi, J.L., Yan, D.S., Holmes, J.D., Adv. Funct. Mater. 14 (2004), 544–552.
61. Anand, N., Reddy, K.H.P., Rao, K.S.R., Burri, D.R., Catal. Lett. 141 (2011), 1355–1363.