A one-pot synthesis of 1,2-Dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-one derivatives catalyzed by perchloric acid supported on silica (HClO 4/SiO2) in the absence of solvent

Journal of the Iranian Chemical Society

Volumn 7, Issue 3, 2010, Pages 770-774

  Ahangar, H Abbastabar ^a   Mahdavinia, G H ^b   Marjani, K ^a   Hafezian, A ^a  

^a Teacher Training University   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

HClO4 SiO2; Heterogeneous catalyst; Naphthoxazine 3 one; One pot; Solvent free reaction

Indexed keywords

EID: 77955969807     PISSN: 1735207X     EISSN: 17352428     Source Type: Journal    
DOI: 10.1007/bf03246067     Document Type: Article

References (39)

1. A. Domiling, I. Ugi, Angew. Chem. Int. Ed. 39 (2000) 3168.
2. L.Weber, K. Illegen, M. Almstetter, Synlett (1999) 366.
3. A. Strecker, Liebigs. Ann. Chem. 75 (1850) 27.
4. D. Pizzirani, M. Roberti, M. Recanatini, Tetrahedron Lett. 48 (2007) 7120.
5. R.S. Kumar, S. Perumal, Tetrahedron Lett. 48 (2007) 7164.
6. D. Dallinger, N.Y. Gorobets, C.O. Kappe, Org. Lett. 5 (2003) 1205.
7. U. Bora, A. Saikia, R.C. Boruah, Org. Lett. 5 (2003) 435.
8. A. Shaabani, R. Ghadari, A. Rahmati, A.H. Rezayan, J. Iran. Chem. Soc. 6 (2009) 710.
9. M.A. Zolfigol, I. Mohammadpoor-Baltork, M. Shiri, J. Iran. Chem. Soc. 5 (2008) 90 and references cited therein.
10. A. Corma, H. Garcia, Adv. Synth. Catal. 348 (2006) 1391.
11. A.K. Chakraborthi, R. Gulhane, Chem. Commun. (2003) 1896.
12. V.T. Kamble, V.S. Jamode, N.S. Joshi, A.V. Biradar, R.Y. deshmukh, Tetrahedron Lett. 47 (2006) 5573
13. S. Rudrawar, R.C. Besra, A.K. Chakraborti, Synthesis (2006) 2767.
14. A.T. Khan, T. Pravin, L.H. Choudhury, Synthesis (2006) 2497.
15. A. Agarwal, Y.D. Vankar, Carbohydrate Res. 340 (2005) 1661
16. A.T. Khan, S. Ghosh, L.H. Choudhury, Eur. J. Org. Chem. (2006) 2226.
17. G. Agnihotri, A.K. Misra, Tetrahedron Lett. 47 (2006) 3653
18. M. Maheswara, V. Siddaiah, G.L.V. Damu, C.V. Rao, ARKIVOC (2006) 201.
19. V.T. Kamble, K.R. Kadam, N.S. Joshi, D.B. Muley, Catal. Commun. 8 (2007) 498.
20. Y. Du, G. Wei, S. Cheng, Y. Hua, R.J. Linhardt, Tetrahedron Lett. 47 (2006) 307.
21. A.K. Chakraborthi, S.V. Chankeshwara, Org. Biomol. Chem. 4 (2006) 2769.
22. S. Kantevari, S.V.N. Vuppalapati, D.O. Biradar, L. Nagarapu, J. Mol. Catal. A: Chem. 266 (2006) 109.
23. M. Narasimhulu, T.S. Reddy, K.C. Mahesh, P. Prabhakar, C.B. Rao, Y. Venkateswarlu, J. Mol. Catal. A: Chem. 266 (2006) 114.
24. M.A. Bigdeli, M.M. Heravi, G.H. Mahdavinia, J. Mol. Catal. A: Chem. 275 (2007) 25.
25. A.S. Girgis, Pharmazie (2000) 466.
26. N. Latif, N. Mishriky, F.M. Assad, Aust. J. Chem. 35 (1982) 1037.
27. Y. Wang, X. Li, K. Ding, Tetrahedron: Asymmetry 13 (2002) 1291.
28. K. Ikeda, T. Morimoto, M. Sekia, Chem. Pharm. Bull. (1980) 1178.
29. I. Szatmari, A. Hetenyi, L. Lazar, F. Fulop, J. Hetrocyclic Chem. 41 (2004) 367.
30. C. Cimarelli, G. Palmieri, E. Volpini, Can. J. Chem. 82 (2004) 1341.
31. M. Dabiri, A.S. Delbari, A. Bazgir, Synlett (2007) 821.
32. M.A. Bigdeli, M.M. Heravi, G.H. Mahdavinia, Catal. Commun. 8 (2007) 1595.
33. M.A. Bigdeli, S. Jafari, G.H. Mahdavinia, H. Hazarkhani, Catal. Commun. 8 (2007) 1641.
34. M.A. Bigdeli, A. Rahmati, H. Abbasi-Ghadim, G.H. Mahdavinia, Tetrahedron Lett. 48 (2007) 4575.
35. C.O. Kappe, J. Org. Chem. 62 (1997) 7201.
36. S.R. Angle, J.D.Rainer, Z. Woytowiez, J. Org. Chem. 62 (1997) 5884.
37. A.T. Kahan, L.H. Choudhury, S. Ghosh, J. Mol. Cat. A: Chem. 255 (2006) 230.
38. P. Tiwari, A.K. Misra, Tetrahedron Lett. 47 (2006) 3573.
39. A. Agarwal, S. Rani, Y.D. Vankar, J. Org. Chem. 69 (2004) 6137.