Polyvinylpolypyrrolidone-bound boron trifluoride (PVPP-BF 3); A mild and efficient catalyst for synthesis of 4-metyl coumarins via the Pechmann reaction

Comptes Rendus Chimie

Volumn 15, Issue 6, 2012, Pages 530-532

  Mokhtary, Masoud ^a   Najafizadeh, Faranak ^b  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

4 Methyl coumarin; Boron trifluoride; Ethyl acetoacetate; Pechmann reaction; Polyvinylpolypyrrolidone

Indexed keywords

EID: 84862688176     PISSN: 16310748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crci.2012.03.004     Document Type: Article

References (40)

1. J.J. Yourick, and R.L. Bronaugh J. Appl. Toxicol. 17 1997 153
2. G.J. Keating, R. Okennedy, and R.D. Thornes Coumarins: biology, applications and mod of action 1997 John Wiley & Sons New York
3. H. Yamazaki, M. Tanaka, and T. Shimada J. Chromatogr. B 721 1999 13
4. M.E.F. Izquierdo, J.Q. Granados, V.M. Mir, and M.C.L. Martinez Food. Chem. 70 2000 251
5. R.F. Zhang, H.P. Zhang, and J.C. Shen Synth. Metal. 106 1999 157
6. J.C. de Melo, and P.F. Fernandes J. Mol. Struct. 565 2001 69
7. B. Cohen, and D. Huppert J. Phys. Chem. A 105 2001 7157
8. T. Eckardt, V. Hagen, B. Schada, R. Schmidt, C. Schweitzer, and J. Bending J. Org. Chem. 67 2002 703
9. R. Jakubiak, T.J. Bunning, R.A. Vaia, L.V. Natarajan, and V.P. Tondiglia Adv. Mater. 15 2003 241
10. A.J. Killard, R. Okennedy, and D.P. Bogan J. Pharm. Biomed. Anal. 14 1996 1585
11. S.J. Semple, S.F. Nobbs, S.M. Pyke, G.D. Reynolds, and R.L.P. Flower J. Ethnopharmacol. 68 1999 283
12. G. Hirsh, V. Fuster, J. Ansell, and J.L. Halperin J. Am. Coll. Cardiol. 41 2003 1633
13. M. Pisklak, D. Maciejewska, F. Herold, and I. Wawer J. Mol. Struct. 649 2003 169 176
14. S.R. Trenor, A.R. Shultz, B.J. Love, and T.E. Long Chem. Rev. 104 2004 3059
15. C.M. Liu, J.J. Qiu, R. Bao, C. Zhao, X.J. Cheng, Y. Xnu, and Y. Zhou React. Func. Polym. 66 2006 455
16. C.J. Tsai, and Y. Chen React. Func. Polym. 66 2006 1327
17. E. Knoevenagel Ber. Dtsch. Chem. Ges. Berlin 37 1904 4461
18. A.M. Song, X.B. Wang, and K.S. Lam Tetrahedron Lett. 44 2003 1755
19. C.H. Schroeder, and K.P. Link J. Am. Chem. Soc. 75 1953 1886
20. C. Wiener, C.H. Schroeder, and K.P. Link J. Am. Chem. Soc. 79 1957 5301
21. E.C. Horning Org. Synth. 3 1955 281
22. S. Frere, V. Thiery, and T. Besson Tetrahedron Lett. 42 2001 2791
23. K.M. Potdar, S.S. Mohile, and M.M. Salunkhe Tetrahedron Lett. 42 2001 9285
24. D.S. Bose, A.P. Rudradas, and M.H. Babu Tetrahedron Lett. 43 2002 9195
25. A. Shockravi, H. Valizadeh, and M.M. Heravi Phosphorus Sulfur Silicon 177 2002 2835
26. P.R. Singh, D.U. Singh, and S.D. Samant Synlett. 2004 1909
27. S.K. De, and R.A. Gibbs Synthesis 2005 1231
28. B.S. Kumar, P.S. Kumar, N. Srinivasulu, B. Rajitha, Y.T. Reddy, P.N. Reddy, and R.H. Udupi Chem. Heterocycl. Comp. 42 2006 172
29. A. Hegedus, and Z. Hell Catal. Lett. 112 2006 105
30. J.C. Rodríguez-Domínguez, and G. Kirsch Synthesis 2006 1895
31. M. Maheswara, V. Siddaiah, G.L.V. Damu, Y.K. Rao, and C.V. Rao J. Mol. Catal. A Chem. 255 2006 49
32. J.C. Rodríguez-Domínguez, and G. Kirsch Tetrahedron Lett. 47 2006 3279
33. R. Torviso, D. Mansilla, A. Belizan, E. Alesso, G. Moltrasio, P. Vazquez, L. Pizzio, M. Blanco, and C. Caceres Appl. Catal. A Gen. 339 2008 53
34. K.K. Upadhyay, R.K. Mishra, and A. Kumar Catal. Lett. 121 2008 118
35. B. Karimi, and D. Zareyee Org. Lett. 10 2008 3989
36. S.V. Ley, I.R. Baxendale, R.N. Bream, P.S. Jackson, A.G. Leach, D.A. Longbottom, M. Nesi, J.S. Scott, R.I. Storer, and S.J. Taylor J. Chem. Soc. Perkin Trans. 1 2000 3815
37. C. Liu, S. Cui, Z. Wang, and X. Zhang J. Phys. Chem. B 109 2005 14807
38. M.M. Lakouraj, and M. Mokhtary Monatsh. Chemie 140 2009 53
39. K. Wilson, and J.H. Clark Chem. Commun. 1998 2135
40. K. Wilson, D.J. Adams, G. Rothenberg, and J.H. Clark J. Mol. Catal. A Chem. 156 2000 309