Phosphotungstic acid catalysed synthesis of β-enamino compounds under solvent-free conditions

Journal of Chemical Research

Volumn , Issue 12, 2007, Pages 696-698

  Li, Geng Chen ^a  

^a SHIJIAZHUANG TIEDAO UNIVERSITY   (China)

Author keywords

1,3 Dicarbonyl compounds; Amines; Enamino esters; Enaminones; Phosphotungstic acid; Solvent free conditions

Indexed keywords

EID: 44949145170     PISSN: 03082342     EISSN: None     Source Type: Journal    
DOI: 10.3184/030823407X273488     Document Type: Article

References (56)

1. G. Sartori and R. Maggi, Chem. Rev., 2006, 106, 1077.
2. J.H. Clark, Acc. Chem. Res., 2002, 35, 791.
3. I.V. Kozhevnikov, Chem. Rev., 1998, 98, 171.
4. M. Misono, I. Ono, G. Koyano and A. Aoshima, Pure Appl. Chem., 2000, 72, 1305.
5. M. Misono, Chem. Commun., 2001, 1141.
6. I.V. Kozhevnikov, Catal. Rev., 1995, 37, 311.
7. M.N. Timofeeva, Appl. Catal A: Gen., 2003, 256, 19.
8. K. Lan, S. Fen and Z.X. Shan, Aust. J. Chem., 2007, 60, 80.
9. M.H. Bhure, C.V. Rode, R.C. Chikate, N. Patwardhan and S. Patil, Catal. Commun., 2007, 8, 139.
10. R. Maheswari, K. Shanthi, T. Sivakumar and S. Narayanan, Appl. Catal A: Gen., 248, 291 (2003).
11. E.F. Kozhevnikova, J. Quartararo and I.V. Kozhevnikov, Appl. Catal A: Gen., 2003, 245, 69.
12. M.M. Heravi, F. Derikvand and F.F. Bamoharram, Synth. Commun., 2006, 36, 3109.
13. E. Rafiee, F. Torka and M. Joshaghani, Bioorg. Med. Chem. Lett., 2006, 16, 1221.
14. S.V. Bhilare, A.R. Deorukhkar, N.B. Darvatkar, M.S. Rasalkar and M.M. Salunkhe, J. Mol. Catal. A: Chem., 2007, 270, 123.
15. E.J.L. Lana, K.A. da Silva Rocha, I.V. Kozhevnikov and E.V. Gusevskaya, J. Mol. Catal. A: Chem., 2006, 243, 258.
16. J.-Y. He, F.-X. Gao and R.-M. Hua, Chin. J. Chem., 2005, 23, 1275.
17. T.-S. Jin, J.-C. Xiao, Y-X. Chen and T.-S. Li, J. Chem. Res. (S), 2004, 190.
18. G. Sivaprasad, R. Rajesh and P.T. Perumal, Tetrahedron Lett., 2006, 47, 1783.
19. B.R. Jermy and A. Pandurangan, Catal. Commun., 2006, 7, 921.
20. B.C. Mishra, D. Kumar and V.S. Rao, Catal. Commun., 2006, 7, 457.
21. A. Heydari, H. Hamadi and M. Pourayoubi, Catal. Commun., 2007, 8, 1224.
22. A. Heydari, R.K. Shiroodi, H. Hamadi, M. Esfandyari and M. Pourayoubi, Tetrahedron Lett., 2007, 48, 5865.
23. H. Firouzabadi, N. Iranpoor, A.A. Jafari and M.R. Jafari, J. Mol. Catal. A: Chem., 247, 14 (2006).
24. H. Firouzabadi, N. Iranpoor and A.A. Jafari, J. Organomet. Chem., 2005, 690, 1556.
25. H. Firouzabadi, N. Iranpoor and A.A. Jafari, Synlett, 2005, 299.
26. M. Li, W.-S. Guo, L.-R. Wen and H.-Z. Yang, Chin. J. Org. Chem., 2006, 26, 1192.
27. H.M.C. Ferraz and E.R.S. Goncalo, Quimica Nova, 2007, 30, 957.
28. K.M. Al-Zaydi and L.M. Nhari, Oriental J. Chem., 2006, 22, 1.
29. M.A. Al-Shiekh, Org. Prep. Proced. Int., 2005, 37, 223.
30. G. Palmieri and C. Cimarelli, Arkivoc, 2006, (vi) 104.
31. G. Dannhardt, A. Bauer and U. Nowe, J. Prakt. Chem., 1998, 340, 256.
32. Z.-H. Zhang, L. Yin and Y.-M. Wang, Adv. Synth. Catal., 2006, 348, 184.
33. P.G. Baraldi, D. Simoni and S. Manfredini, Synthesis, 1993, 902.
34. D.F. Martin, G.A. Janusonis and B.B. Martin, J. Am. Chem. Soc., 1961, 83, 73.
35. G. Bartoli, M. Bosco, M. Locatelli, E. Marcantoni, P. Melchiorre and L. Sambri, Synlett, 2004, 239.
36. M.M. Khodaei, A.R. Khosropour and M. Kookhazadeh, Synlett, 2004, 1980.
37. A. Arcadi, G. Bianchi, S. Di Giuseppe and F. Marinelli, Green Chem., 2003, 5, 64.
38. A.R. Khosropour, M.M. Khodaei and M. Kookhazadeh, Tetrahedron Lett, 45, 2004, 1725.
39. Z.-H. Zhang and J.-Y. Hu, J. Braz. Chem. Soc., 2006, 17, 1447.
40. L.-P. Mo, S.-F. Liu and W.-Z. Li, J. Chin. Chem. Soc., 2007, 54, 879.
41. V. Sridharan, C. Avendaño and J.C. Menéndez, Synlett, 2007, 881.
42. F. Epifano, S. Genovese and M. Curini, Tetrahedron Lett., 2007, 48, 2717.
43. R. Varala, S. Nuvula and S.R. Adapa, Aust. J. Chem., 2006, 59, 921.
44. Z.-H. Zhang, Z.-C. Ma and L.-P. Mo, Indian J. Chem., 2007, 46B, 535.
45. J. Lin and L.-F. Zhang, Monatsh. Chem., 2007, 138, 77.
46. Z.-H. Zhang, T.-S. Li and J.-J. Li, Catal. Commun., 2007, 8, 1615.
47. R.K. Vohra, J.-L. Renaud and C. Bruneau, Collect. Czech. Chem. Commun., 2005, 70, 1943.
48. J.S. Yadav, V.N. Kumar, R.S. Rao, A.D. Priyadarshini, P.P. Rao, B.V.S. Reddy and K. Nagaiah, J. Mol. Catal. A: Chem., 2006, 256, 234.
49. S. Gogoi, R. Bhuyan and N.C. Barua, Synth. Commun., 2005, 35, 2811.
50. M.E.F. Braibante, H.T.S. Braibante, A.F. Morel, C.C. Costa and M.G. Lima, J. Braz. Chem. Soc., 2006, 17, 184.
51. A.R. Gholap, N.S. Chakor, T. Daniel, R.J. Lahoti and K.V. Srinivasan, J. Mol. Catal. A: Chem., 2006, 245, 37.
52. Y.-H. Gao, Q.-H. Zhang and J.-X. Xu, Synth. Commun., 2004, 34, 909.
53. F.C. Silva, M.C.B.V. De Souza, V.F. Ferreira, S.J. Sabino and O.A.C. Antunes, Catal. Commun., 2004, 5, 151.
54. Z.-H. Zhang and L.-M. Song, J. Chem. Res., 2006, 817.
55. R.S. Bhosale, P.A. Suryawanshi, S.A. Ingle, M.N. Lokhande, S.P. More, S.B. Mane, S.V. Bhosale and R.P. Pawar, Synlett, 2006, 933.
56. B. Das, K. Venkateswarlu, A. Majhi, M.R. Reddy, K.N. Reddy, Y.K. Rao, K. Ravikumar and B. Sridhar, J. Mol. Catal. A: Chem., 2006, 246, 276.