Use of nano-CuY zeolite as an efficient and eco-friendly nanocatalyst for facile synthesis of perimidine derivatives

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• 作者：Mehdi Kalhor (1)
  Nooshin Khodaparast (1)
  
  1. Department of Chemistry ; Payame Noor University ; 19395-4697 ; Tehran ; Islamic Republic of Iran
  
• 关键词：Perimidine ; Catalyst ; Arylaldehyde ; Transition nano ; metal zeolite
• 刊名：Research on Chemical Intermediates
• 出版年：2015
• 出版时间：May 2015
• 年：2015
• 卷：41
• 期：5
• 页码：3235-3242
• 全文大小：333 KB
• 参考文献：1. Undheim, K, Benneche, C In: Katritzky, AR, Rees, CW, Scriven, EF eds. (1996) Comprehensive Heterocyclic Chemistry II. Pergamon, Oxford
  2. Pozharskii, AF, Dalnikovskaya, VV (1981) Russ. Chem. Rev. 50: pp. 816 CrossRef
  3. Bu, X, Deady, LW, Finlay, GJ, Baguley, BC, Denny, WA (2001) J. Med. Chem. 44: pp. 2004 CrossRef
  4. Herbert, JM, Woodgate, PD, Denny, WA (1987) J. Med. Chem. 30: pp. 2081 CrossRef
  5. Panchasara, DP, Pande, S (2009) E-J. Chem. 6: pp. 591 CrossRef
  6. Luthin, DR, Rabinovich, AK, Bhumralkar, DR, Youngblood, KL, Bychowski, RA, Dhanoa, DS, May, JM (1999) Bioorg. Med. Chem. Lett. 9: pp. 765 CrossRef
  7. Bassyouni, FA, Abu-Bakr, SM, Hegab, KH, El-Eraky, W, Beih, AA, Abdel Rehim, ME (2012) Res. Chem. Intermed. 38: pp. 1527 CrossRef
  8. Paragamian, V, Baker, MB, Puma, BM, Reale, J (1968) J. Heterocycl. Chem. 5: pp. 591 CrossRef
  9. Shaabani, A, Maleki, A (2008) Chem. Pharm. Bull. 56: pp. 79 CrossRef
  10. Hendrickson, JB, Hussoin, MS (1987) J. Org. Chem. 52: pp. 4137 CrossRef
  11. Vanden Eynde, JJ, Delfosse, F, Mayence, A, Haverbeke, YV (1995) Tetrahedron 51: pp. 5813 CrossRef
  12. Yavari, I, Mostafavi, H, Tahmassebi, D, Hekmat-Shoar, R, Monatsh, (1997) Chem. 128: pp. 675
  13. Ozeryanskii, VA, Filatova, EA, Sorokin, VI, Pozharskii, AF (2001) Russ. Chem. Bull. 50: pp. 846 CrossRef
  14. Maquestiau, A, Berte, L, Mayence, A, Vanden Eynd, L (1991) Synth. Commun. 21: pp. 2171 CrossRef
  15. Mobinikhaledi, A, Steel, PJ (133) Synth. React. Inorg. Met.-Org. Chem. 39: pp. 2009
  16. Zhang, S-L, Zhang, J-M (2008) Chin. J. Chem. 26: pp. 185 CrossRef
  17. Zhang, J, Zhang, S (2007) Synth. Commun. 37: pp. 2615 CrossRef
  18. Belmonte, MM, Escudero-Ad谩n, EC, Benet-Buchholz, J, Haak, RM, Kleij, AW (2010) Eur. J. Org. Chem. 2010: pp. 4823 CrossRef
  19. Mobinikhaledi, A, Moghanian, H, Sasani, F (2010) Int.J. Green Nanotechnol Phys. Chem. 2: pp. 47 CrossRef
  20. Maloshitskaya, O, Sinkkonen, J, Ovcharenko, VV, Zelenin, KN, Pihlaj, K (2004) Tetrahedron 60: pp. 6913 CrossRef
  21. Deady, LW, Rodemann, T (1998) J. Heterocycl. Chem. 35: pp. 1417 CrossRef
  22. Morita, N, Dickstein, JI, Miller, SI (1979) J. Chem. Soc. Perkin Trans. 1: pp. 2103 CrossRef
  23. Yavari, I, Jahanimoghaddam, F, Adib, F, Bijanzadeh, HR (2002) Tetrahedron 58: pp. 6901 CrossRef
  24. Smellie, IAS, Fromm, A, Paton, RM (2009) Tetrahedron Lett. 50: pp. 4104 CrossRef
  25. Mobinikhaledi, A, Foroughifar, N, Basaki, N (2009) Turk. J. Chem. 33: pp. 555
  26. Tajbakhsh, M, Heravi, MM, Mohajerani, B, Ahmadi, A (2006) J. Mol. Catal. A 247: pp. 213 CrossRef
  27. Sheldon, RA, Downing, RS (1999) Appl. Catal. A 189: pp. 163 CrossRef
  28. Bournay, L, Casanave, D, Delfort, B, Hillion, G, Chodorge, JA (2005) Catal. Today 106: pp. 190 CrossRef
  29. Yang, YX, Singh, RK, Webley, PA (2008) Adsorption 14: pp. 265 CrossRef
  30. Centi, G, dall鈥橭lio, L, Perathoner, S, Generali, P (2000) Ind. Eng. Chem. Res. 39: pp. 131 CrossRef
  31. Salavati-Niasari, M (2007) Trans. Met. Chem. 32: pp. 1 CrossRef
  32. Vijaikumar, S, Subramanian, T, Pitchumani, K (2008) J. Nanomater. 49: pp. 1818
  33. Tang, X-J, Fei, J-H, Hou, Z-Y, Zheng, X-M, Lou, H (2008) Energy Fuels 22: pp. 2877 CrossRef
  34. Zendehdel, M, Khanmohamadi, H, Mokhtari, M (2010) J. Chin. Chem. Soc. 57: pp. 205 CrossRef
  35. Mobinikhaledi, A, Foroughifar, N, Bodaghi-Fard, MA, Moghanian, H, Ebrahimi, S, Kalhor, M (2009) Synth. Commun. 39: pp. 1166 CrossRef
  36. Kalhor, M, Mobinikhaledi, A, Jamshidi Res, J (2013) Chem. Intermed. 39: pp. 3127 CrossRef
  37. Kalhor, M, Khodaparast, N, Zendehdel, M (2013) Lett. Org. Chem. 10: pp. 573 CrossRef
  38. D.W. Breck, N.Y. Tonawanda, Assigned to Union Corbide pat. No 3130007 (1964)
  39. Zendehdel, M, Mobinikhaledi, A, Hasanvand, JF (2007) J. Incl. Phenom. Macrocycl. Chem. 59: pp. 41 CrossRef
  
• 刊物类别：Chemistry and Materials Science
• 刊物主题：Chemistry
  Catalysis
  Physical Chemistry
  Inorganic Chemistry
  
• 出版者：Springer Netherlands
• ISSN：1568-5675

文摘

A simple and practical procedure is described for synthesis of 2-aryl dihydroperimidines. One-pot reaction of 1,8-diaminonaphthalene with a variety of aromatic aldehydes, in the presence of nano-copper Y zeolite as highly efficient catalyst, was performed in ethanol at room temperature. The CuY zeolite nanocatalyst was characterized by scanning electron microscopy (SEM). Novel compounds were characterized by spectroscopic and spectrometric analyses. This environmentally benign and clean synthetic procedure has several advantages, including the availability, safety, and reusability of the catalyst, high yields, short reaction times, and easy and rapid isolation of the product.