FeCl 3.nano SiO 2: An efficient heterogeneous nano catalyst for the synthesis of 14-Aryl-14H-dibenzo[a,j]xanthenes and 1,8-Dioxo-octahydro-xanthenes under solvent-free conditions

South African Journal of Chemistry

Volumn 65, Issue , 2012, Pages 191-195

  Safaei Ghomi, Javad ^a   Ghasemzadeh, Mohammad Ali ^a   Zahedi, Safura ^a  

^a UNIVERSITY OF KASHAN   (Iran)

Author keywords

Ferric chloride; Multi component reactions; Nano silica; Solvent free; Xanthenes

Indexed keywords

EID: 84866115018     PISSN: 03794350     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (47)

1. M.H. Alizadeh, H. Razavi and F.F. Bamoharram, J. Mol. Catal A: Chem., 2003, 206, 89-93.
2. G.M. Ziarani, A. Badiei, F. Shahjafari and T. Pourjafar, S. Afr. J. Chem., 2012, 65, 10-13.
3. G.S. McCarty and P.S. Weiss, Chem. Rev., 1999, 99, 1983-1990.
4. N. Ahmed and J.E. Van Lier, Tetrahedron Lett., 2006, 47, 2725-2729.
5. Q. Dang, B.S. Brown and M.D. Erion, Tetrahedron Lett., 2000, 41, 6559-6562.
6. A. Corma and H. Garcia, Chem Rev., 2002, 102, 3837-3792.
7. H.M. Hagiwara, N. Sekifuji, T. Tsubokawa and T. Hoshi, Chem Lett., 2009, 38, 926-933.
8. R.W. Lambert, J.A. Martin, J.H. Merrett, K.E.B. Parkes and G.J. Thomas, PCT Int. Appl. WO9706178, 1997
9. Chem. Abstr., 1997, 126, p212377y.
10. G.J. Bennett and H.-H. Lee, Phytochem., 1989, 28, 967-998.
11. T. Hideo and J. Teruomi, Jpn. Tokkyo Koho JP56005480, 1981; Chem. Abstr. 1981, 95, 80922b.
12. V. Peres, T.J. Nagem and F.F. de Oliveira, Phytochem., 2000, 55, 683-710.
13. H.N. Hafez, M.I. Hegab, I.S. Ahmed-Farag and A.B.A. El-Gazzar, Bioorg. Med. Chem. Lett., 2008, 18, 4538-4543.
14. M.M.M. Pinto, M.E. Sousa and M.S.J. Nascimento, Curr. Med. Chem., 2005, 12, 2517-2538.
15. S.M. Menchen, S.C. Benson, J.Y.L. Lam, W. Zhen, D. Sun, B.B. Rosenblum, S.H. Khan and M. Taing, U.S. Patent, US 6583168, 2003
16. Chem. Abstr., 2003, 139, p54287f.
17. M. Ahmad, T.A. King, K. Do-Kyeong, B.H. Cha and L. Jongmin, J. Phys. D: Appl. Phys., 2002, 35, 1473-1476.
18. C.G. Knight and T. Stephens, Biochem. J., 1989, 258, 683-687.
19. G. Casiraghi, G. Casnati and M. Cornia, Tetrahedron Lett., 1973, 14, 679-682.
20. A. Bekaert, J. Andrieux and M. Plat, Tetrahedron Lett., 1992, 33, 2805-2806.
21. D.W. Knight and P.B. Little, J. Chem. Soc. Perkin Trans. I., 2001, 4, 1771-1777.
22. C.W. Kuo and J.M. Fang, Synth. Commun., 2001, 31, 877-892.
23. J.Q. Wang and R.G. Harvey, Tetrahedron., 2002, 58, 5927-5931.
24. A. Jha and J. Beal, Tetrahedron Lett., 2004, 45, 8999-9001.
25. S. Allameh, A. Davoodnia and A. Khojastehnezhad, Chin. Chem. Lett., 2012, 23, 17-20.
26. D. Prasd and M. Nath, Catal. Sci. Technol., 2012, 2, 93-96.
27. M.A. Zolfigol, A.R. Moosavi-Zare, P. Arghavani-Hadi, A. Zare, V. Arghavani-Hadi and G. Arghavani-Hadi, RSC Advances, 2012, 2, 3618-3620.
28. K. Tabatabaeian, A. Khorshidi, M. Mamaghani and A. Dadashi, Synth. Commun., 2011, 41, 1427-1434.
29. N.G. Khaligh, Ultrason Sonochem., 2012, 19, 736-739.
30. A. Zare-Bidaki and A. Davoodnia, Bull. Korean Chem. Soc., 2012, 33, 1154-1158.
31. R. K. FischerHunnur, B. Sunilkumar, P.S. Kumar, N. Srinivasulu, R.H. Udupi andV. Himabindu, Chem. Heterocycl. Compd., 2008, 44, 143-147.
32. E. Soleimani, M. Zainal and S. Lotfi, Lett. Org. Chem., 2011, 8, 573-576.
33. Z. Karimi-Jaberi, S. Zoleykha Abbasi, B. Pooladian and M. Jokar, E-J Chem., 2011, 8, 1895-1899
34. E. Soleimani, M.H. Khodei and A.T. Kal Koshvandi, Chin. Chem. Lett., 2011, 22, 927-930.
35. G. Mohammadi Ziarani, A.-R. Badiei and M. Azizi, Scientia Iranica C., 2011, 18, 453-457
36. M. Hong and C. Cai, J. Fluorine Chem., 2009, 130, 989-992.
37. H. Eshghi, M. Bakavoli andH. Moradi, Org. Prep. Proced. Int., 2011, 43, 302-307.
38. R. Kumar, G.C. Nandi, R.K. Verma and M.S. Singh, Tetrahedron Lett., 2010, 5, 442-445.
39. A. Rahmatpour and J. Aalaie, Heteroat. Chem., 2011, 22, 51-54.
40. T.S. Jin, J.S. Zhang, A.Q. Wang and T.S. Li, Synth. Commun., 2005, 35, 2339-2345.
41. B.R. Madje, M.B. Ubale, J.V. Bharad and M.S. Shingare, S. Afr. J. Chem., 2010, 63, 36-39.
42. A.N. Dadhania, V.K. Patel and D.K. Raval, C. R. Chimie., 2012, 15, 378-383.
43. A. Rahmati, Chin. Chem. Lett., 2010, 21, 761-764.
44. G. Song, B. Wang, H. Luo and L. Yang, Catal. Commun., 2007, 8, 673-676.
45. B. Das, P. Thirupathi, I. Mahender, K.R. Reddy, B. Ravikanth and L. Nagarapu,. Catal. Commun., 2007, 8, 535-538.
46. A. IIangovan, S. Malayappasamy, S. Muralidharan and S. Maruthamuthu, Chem. Cent. J., 2011, 5, 81-86.
47. M. Seyyedhamzeh, P. Mirzaei and A. Bazgir, Dyes Pigm., 2008, 76, 836-839.