Periodic mesoporous silica chloride (PMSCl) as an efficient and recyclable catalyst for the Pechmann reaction

Catalysis Communications

Volumn 12, Issue 15, 2011, Pages 1432-1436

  Karimi, Babak ^a   Behzadnia, Hesam ^a  

^a INSTITUTE FOR ADVANCED STUDIES IN BASIC SCIENCES IASBS   (Iran)

Author keywords

Coumarins; Pechmann reaction; Periodic mesoporous silica chloride; PMSCl

Indexed keywords

COUMARINS; HEXAGONAL STRUCTURES; MESOPOROUS SILICA; PECHMANN REACTION; PMSCL; RECYCLABLE CATALYST; SOLVENT FREE CONDITIONS;

CATALYSTS; CHLORINE COMPOUNDS; MESOPOROUS MATERIALS; PHENOLS; SILICA;

PERIODIC STRUCTURES;

EID: 79959272430     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2011.05.019     Document Type: Article

References (49)

1. R.O. Kennedy, and R.D. Thornes Coumarins: Biology Applications and Mode of Action 1997 John Wiley and Sons Chichester
2. O. Snow Amphetamine syntheses Psychoactive Synth. Ser.: USA 1 1998
3. S.M. Sethna, and N.M. Shah Chem. Rev. 36 1945 1 62
4. X.T. Liang, and W.S. Fang Medicinal chemistry of bioactive natural products 2006 John Wiley & Sons Hoboken, New Jersey
5. G. Cavettos, G.M. Nano, G. Palmisano, and S. Tagliapietra Tetrahedron-Asymmetry 12 2001 707 709
6. R.L. Shriner Org. React. 1 1942 1 37
7. I. Yavari, R. Hekmat-Shoar, and A. Zonouzi Tetrahedron Lett. 39 1998 2391 2392
8. A. Shaabani, R. Ghadari, A. Rahmati, A.H. Rezayan, and J. Iran Chem. Soc. 6 2009 710 714
9. G. Jones Org. React. 15 1967 204 599
10. G. Brufola, F. Fringuelli, O. Piermatti, and F. Pizzo Heterocycles 43 1996 1257 1266
11. J.R. Johnson Org. React. 1 1942 210 265
12. V.P. Hong, and K.J. lee Synthesis 2005 33 38
13. H. Pechmann, and C. Duisberg Chem. Ber. 17 1884 929
14. H. Pechmann, and C. Duisberg Chem. Ber. 16 1883 2119 2128
15. D.S. Bose, A.P. Rudradas, and M.H. Babu Tetrahedron Lett. 43 2002 9195 9197
16. A.C. Khandekar, and B.M. Khadilkar Synlett 2002 152 154
17. P.R. Singh, D.U. Singh, and S.D. Samant Synlett 2004 1909 1912
18. Y. Gu, J. Zhang, Z. Duan, and Y. Deng Adv. Synth. Catal. 347 2005 512 516
19. M.K. Potdar, M.S. Rasalkar, S.S. Mohile, and M.M. Salunkhe J. Mol. Catal. A: Chem. 235 2005 249 252
20. S.K. De, and R.A. Gibbs Synthesis 2005 1231 1233
21. J.C. Rodríguez-Domínguez, and G. Kirsch Synthesis 2006 1895 1897
22. M.S. Manhas, S.N. Ganguly, S. Mukherjee, A.K. Jain, and A.K. Bose Tetrahedron Lett. 47 2006 2423 2425
23. G. Bratulescu Synthesis 2008 2871 2873
24. E.V.O. John, and S.S. Israelstam J. Org. Chem. 26 1961 240 242
25. T.S. Li, Z.H. Zhang, F. Yang, and C.G. Fu J. Chem. Res. 1998 38 39
26. M.C. Laufer, H. Hausmann, and W.F. Hölderich J. Catal. 218 2003 315 320
27. R. Sabou, W.F. Hoelderich, D. Ramprasad, and R. Weinand J. Catal. 2005 34 37
28. M. Maheswara, V. Siddaiah, G.L.V. Damu, Y.K. Rao, and C.V. Rao J. Mol. Catal. A: Chem. 255 2006 49 52
29. B. Tyagi, M.K. Mishra, and R.V. Jasra J. Mol. Catal. A: Chem. 276 2007 47 56
30. S. Selvakumar, M. Chidambaram, and A.P. Singh Catal. Commun. 8 2007 777 783
31. R. Torviso, D. Mansilla, A. Belizán, E. Alesso, G. Moltrasio, P. Vázquez, L. Pizzio, M. Blanco, and C. Cáceres Appl. Catal. A: Gen. 339 2008 53 60
32. C.T. Kresge, M.E. Leonowicz, W.J. Roth, J.C. Vartuli, and J.S. Beck Nature 359 1992 710 712
33. D. Zhao, J. Feng, Q. Huo, N. Melosh, G.H. Fredrickson, B.F. Chmelka, and G.D. Stucky Science 279 1998 548 552
34. D. Zhao, Q. Huo, J. Feng, B.F. Chmelka, and G.D. Stucky J. Am. Chem. Soc. 120 1998 6024 6036
35. A.P. Wight, and M.E. Davis Chem. Rev. 102 2002 3589 3614
36. A. Corma, and H. Garcia Chem. Rev. 102 2002 3837 3892
37. Z.L. Lu, E. Lindner, and H.A. Mayer Chem. Rev. 102 2002 3543 3578
38. T. Mallat, and A. Baiker Chem. Rev. 104 2004 3037 3058
39. B. Karimi, S. Abedi, J.H. Clark, and V. Budarin Angew. Chem. Int. Ed. 45 2006 4776 4779
40. B. Karimi, A. Biglari, J.H. Clark, and V. Budarin Angew. Chem. Int. Ed. 46 2007 7210 7213
41. B. Karimi, A. Zamani, S. Abedi, and J.H. Clark Green Chem. 2009 109 119
42. B. Karimi, and D. Zareyee Org. Lett. 10 2008 3989 3992
43. B. Karimi, and H. Behzadnia Synlett 2010 2019 2023
44. Y. Kamitori, M. Hojo, R. Masuda, T. Kimura, and T. Yoshida J. Org. Chem. 51 1986 1427 1431
45. J.H. Clark, S.J. Tavener, and S.J. Barlow Chem. Commun. 1996 2429 2430
46. H. Firouzabadi, N. Iranpoor, B. Karimi, and H. Hazarkhani Synlett 2000 263 265
47. H. Firouzabadi, N. Iranpoor, H. Hazarkhani, and B. Karimi J. Org. Chem. 67 2002 2572 2576
48. M.H. Lim, C.F. Blanford, and A. Stein Chem. Mater. 10 1998 467 470
49. D. Margolese, J.A. Melero, S.C. Christiansen, B.F. Chmelka, and G.D. Stucky Chem. Mater. 12 2000 2448 2459