A sulfonic acid functionalized ionic liquid as a homogeneous and recyclable catalyst for the one-pot synthesis of α-aminophosphonates

Tetrahedron Letters

Volumn 50, Issue 29, 2009, Pages 4236-4238

  Akbari, Jafar ^a   Heydari, Akbar ^a  

^a TARBIAT MODARES UNIVERSITY   (Iran)

Author keywords

Aminophosphonates; Functionalized ionic liquid; Homogeneous catalysis; Recycling

Indexed keywords

ALDEHYDE; ALPHA AMINOPHOSPHONATE DERIVATIVE; AMINE; BRONSTED ACID; IONIC LIQUID; KETONE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ONE POT SYNTHESIS; ROOM TEMPERATURE;

EID: 66149182887     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.020     Document Type: Article

References (36)

1. Kafarski P., and Lejczak B. Phosphorus, Sulfur Silicon Relat. Elem. 63 (1991) 1993
2. Allen M.C., Fuhrer W., Tuck B., Wade R., and Wood J.M. J. Med. Chem. 32 (1989) 1652
3. Baylis E.K., Campbell C.D., and Dingwall J.G. J. Chem. Soc., Perkin Trans. 1 (1984) 2845
4. Atherton F.R., Hassal C.H., and Lambert R.W. J. Med. Chem. 29 (1986) 29
5. Maier L. Phosphorus, Sulfur Silicon Relat. Elem. 53 (1990) 43
6. Emsley J., and Hall D. The Chemistry of Phosphorous (1976), Harper and Row, London p 494
7. Meenen E.V., Moonen K., Acke D., and Stevens C.V. Arkivoc i (2006) 31
8. Maier L. Phosphorus, Sulfur Silicon Relat. Elem. 14 (1983) 295
9. Yokomatsu T., Yamagishi T., and Shibuya S.J. Synth. Org. Chem. Jpn. 53 (1995) 881
10. Sardarian A.R., and Kaboudin B. Tetrahedron Lett. 38 (1997) 2543
11. Smith A.B., Yager K.M., and Taylor C.M. J. Am. Chem. Soc. 117 (1995) 10874
12. Smith A.B., Yager K.M., and Taylor C.M. J. Am. Chem. Soc. 116 (1994) 9377
13. Chung S.K., and Kang D.H. Tetrahedron: Asymmetry 7 (1996) 21
14. Ha H.J., and Nam G.S. Synth. Commun. 22 (1992) 1143
15. Afarinkia K., Rees C.W., and Cadogan J.I.G. Tetrahedron 46 (1990) 7175
16. Sasai H., Arai S., Tahara Y., and Shibasaki M. J. Org. Chem. 60 (1995) 6656
17. Hamilton R., Walker B., and Walker B.J. Tetrahedron Lett. 36 (1995) 4451
18. Oshikawa T., and Yamashita M. Bull. Chem. Soc. Jpn. 62 (1989) 3177
19. Laschat S., and Kunz H. Synthesis (1992) 90
20. Hoppe I., Schollkorpf U., Nieger M., and Egert E. Angew. Chem., Int. Ed. Engl. 24 (1985) 1067
21. Petrov K.A., Chauzov V.A., and Erokhina T.S. Usp. Khim. 43 (1974) 2045 Chem. Abstr. 1974, 82, 43486y
22. Atmani A., Combret J.C., Malhiac C., and Kajima Mulengi J. Tetrahedron Lett. 41 (2000) 6045
23. Zon J. Pol. J. Chem. 55 (1981) 643
24. Heydari A., Hamadi H., and Pourayoubi M. Catal. Commun. 8 (2007) 1224
25. Heydari A., and Arefi A. Catal. Commun. 8 (2007) 1023
26. Vahdat S.M., Baharfar R., Tajbakhsh M., Heydari A., Baghbanian S.M., and Khaksar S. Tetrahedron Lett. 49 (2008) 6501
27. Welton T. Chem. Rev. 99 (1999) 2071
28. Earle M.J., and Seddon K.R. Pure Appl. Chem. 72 (2000) 1391
29. Wilkes J.S.J. Mol. Catal. A: Chem. 214 (2004) 11
30. Cole A.C., Jensen J.L., Ntai I., Tran K.L.T., Weaver K.J., Forbes D.C., and Davis Jr. J.H. J. Am. Chem. Soc. 124 (2002) 5962
31. Wang H., Jiang D., and Dai L. Catal. Commun. 9 (2008) 2475
32. Li X., Eli W., and Li G. Catal. Commun. 9 (2008) 2264
33. Cheng G., Duan X., Qi X., and Lu C. Catal. Commun. 10 (2008) 201
34. Yang L., Xu L.W., Zhou W., Li L., and Xia C.G. Tetrahedron Lett. 47 (2006) 7723
35. Ranu B.C., Hajra A., and Jana U. Org. Lett. 1 (1999) 1141
36. Lee S., Park J.H., Kang J., and Lee J.K. Chem. Commun. (2001) 1698