Coumarin synthesis via knoevenagel condensation reaction in 1,1,3,3-N,N,N',N'- tetramethylguanidinium trifluoroacetate ionic liquid

Journal of the Iranian Chemical Society

Volumn 6, Issue 4, 2009, Pages 710-714

  Shaabani, A ^a   Ghadari, R ^a   Rahmati, A ^a   Rezayan, A H ^a  

^a SHAHID BEHESHTI UNIVERSITY   (Iran)

Author keywords

Coumarin; Ionic liquid; Microwave irradiation; Dicarbonyl C H acid

Indexed keywords

EID: 70449674394     PISSN: 1735207X     EISSN: 17352428     Source Type: Journal    
DOI: 10.1007/BF03246160     Document Type: Article

References (31)

1. J.J. Yourick, R.L. Bronaugh, J. Appl. Toxicol. 17 (1997) 153.
2. R. O'Kennedy, R.D. Thornes, Coumarins: Biology, Applications, and Mode of Action, John Wiley & Sons, New York, 1997.
3. B.E. Nielson, V.E. Heywood in The Biology and Chemistry of the Umbelliferae, Academic Press, London, 1971.
4. R.D.H. Murray, J. Mendez, S.A. Brown, The Natural Coumarins, Occurrence, Chemistry and Biochemistry, John Wiely & Sons, New York, 1982.
5. H. Yamazaki, M. Tanaka, T. Shimada, J. Chromatogr. B 721 (1999) 13.
6. M.E.F. Izquierdo, J.Q. Granados, V.M. Mir, M.C.L. Martinez, Food Chem. 70 (2000) 251.
7. S.R. Trenor, A.R. Shultz, B.J. Love, T.E. Long, Chem. Rev. 104 (2004) 3059.
8. S.W. Park, B.S. Seo, E.H. Kim, D.H. Kim, K.J. Paeng, J. Forensic Sci. 41 (1996) 685.
9. E. Knoevenagel, Ber. Dtsch. Chem. Ges Brelin, 37 (1904) 4461.
10. A.M. Song, X.B. Wang, K.S. Lam, Tetrahedron Lett. 41 (2003) 1775.
11. H. von Pechmann, C. Duisberg, Chem. Ber. 37 (1884) 929.
12. R.L. Shriner, Org. React. 1 (1942) 1.
13. N.S. Narasimahan, R.S. Mali, M.V. Barve, Synthesis, (1979) 906.
14. Yavari, R. Hekmat-Shoar, A. Zonouzi, Tetrahedron Lett. 39 (1998) 2391.
15. F.F. Ye, J.R. Gao, W.J. Sheng, J.H. Jia, Dyes Pigments 77 (2008) 556.
16. J. Oyamada, T. Kitamura, Tetrahedron 62 (2006) 6918.
17. M. Maheswara, V. Siddaiah, G.L.V. Damu, Y.K. Rao, C.V. Rao, J. Mol. Catal. A 255 (2006) 49.
18. T. Welton, Chem. Rev. 99 (1999) 2071.
19. P. Wasserscheid, W. Keim, Angew. Chem. Int. Ed. 39 (2000) 3772.
20. R. Sheldon, Chem. Commun. (2001) 2399.
21. A. Shaabani, A. Rahmati, Cat. Lett. 100 (2005) 177.
22. A. Shaabani, A. Rahmati, S. Naderi, Bioorg. Med. Chem. Lett. 15 (2005) 5553.
23. A. Shaabani, A.H. Rezayan, J. Porphyr. Phthalocya. 9 (2005) 617.
24. A. Shaabani, E. Soleimani, A. Maleki, Tetrahedron Lett. 47 (2006) 3031.
25. A. Shaabani, A. Sarvary, A. Rahmati, A.H. Rezayan, Lett. Org. Chem. 4 (2007) 68.
26. A. Shaabani, E. Farhangi, A. Rahmati, Appl. Catal. A 14 (2008) 338.
27. A. Shaabani, E. Soleimani, A.H. Rezayan, A. Sarvari, Org. Lett. 10 (2008) 2581.
28. A. Shaabani, S. Samadi, Z. Badri, A. Rahmati, Cat. Lett. 104 (2005) 39.
29. N.M.M. Mateus, L.C. Branco, N.M.T. Lourenco, C.A.M. Afonso, Green Chem. 5 (2003) 347.
30. F. Bigi, L. Chesini, R. Maggi, G. Sartori, J. Org. Chem. 64 (1999) 1033.
31. A. Song, X. Wang, K.S. Lam, Tetrahedron Lett. 44 (2003) 1755.