Nano ceria catalyzed synthesis of α-aminophosphonates under ultrasonication

Tetrahedron Letters

Volumn 52, Issue 27, 2011, Pages 3499-3504

  Agawane, Sandeep M ^a   Nagarkar, Jayashree M ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Kabachnik Fields reaction; Nano ceria; Solvent free; Ultrasound

Indexed keywords

NANOPARTICLE; PHOSPHONIC ACID DERIVATIVE;

ARTICLE; CATALYST; IRRADIATION; NANOCHEMISTRY; ONE POT SYNTHESIS; POLYMERIZATION; ULTRASOUND;

EID: 79957930322     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.04.112     Document Type: Article

References (56)

1. R.P. Sheridan J. Chem. Inf. Comput. Sci. 42 2002 103 108
2. J.A. Sikosrki, M.J. Miller, D.S. Braccolino, D.G. Cleary, S.D. Corey, J.E. Ream, D. Schnur, A. Shah, and M.C. Walker Phosphorus, Sulfur Silicon Relat. Elem. 76 1993 375 378
3. B. Stowasser, K.-H. Budt, L. Jian-Qi, A. Peyman, and D. Ruppert Tetrahedron Lett. 33 1992 6625 6628
4. F.R. Atherton, C.H. Hassall, and R.W. Lambert J. Med. Chem. 29 1986 29 40
5. A. Peyman, K.-H. Budt, J.S. Paning, B. Stowasser, and D. Ruppert Tetrahedron Lett. 33 1992 4549 4552
6. J.H. Meyer, and P.A. Barlett J. Am. Chem. Soc. 120 1998 4600 4609
7. L. Maier Phosphorus, Sulfur Silicon Relat. Elem. 53 1990 43 67
8. L. Maier, and H. Spoerri Phosphorus, Sulfur Silicon Relat. Elem. 61 1991 69 75
9. J. Emsley, and D. Hall Chemistry of Phosphorus 1976 Harper & Row London pp 494
10. L. Maier, and P. Lea J. Phosphorus, Sulfur Silicon Relat. Elem. 17 1983 1 19
11. P.P. Giannousis, and P.A. Bartlett J. Med. Chem. 30 1987 1603 1609
12. S. Laschat, and H. Kunz Synthesis 1/2 1992 90 95
13. J.S. Yadav, B.V.S. Reddy, S. Raj, K.B. Reddy, and A.R. Prasad Synthesis 15 2001 2277 2280
14. H.J. Ha, and G.S. Nam Synth. Commun. 22 1992 1143 1148
15. T. Yokomatsu, Y. Yoshida, and S. Shibuya J. Org. Chem. 59 1994 7930 7933
16. A. Heydari, H. Hamadi, and M. Pourayoubi Catal. Commun. 8 2007 1224 1226
17. S. Bhagat, and A.K. Chakraborti J. Org. Chem. 72 2007 1263 1270
18. A. Heydari, and A. Arefi Catal. Commun. 8 2007 1023 1026
19. A.K. Bhattacharya, and T. Kaur Synlett 2007 745 748
20. K. Manabe, and S. Kobayashi Chem. Commun. 8 2000 669 670
21. C. Qian, and T. Huang J. Org. Chem. 63 1998 4125 4128
22. B.C. Ranu, A. Hajra, and J. Jana Org. Lett. 1 1999 1141 1143
23. F. Xu, Y. Luo, M. Deng, and Q. Shen Eur. J. Org. Chem. 24 2003 4728 4730
24. H. Firouzabadi, N. Iranpoor, and S. Sobhani Synthesis 16 2004 2692 2696
25. N. Azizi, and M.R. Saidi Eur. J. Org. Chem. 23 2003 4630 4633
26. A. Heydari, A. Karimian, and J. Ipaktschi Tetrahedron Lett. 39 1998 6729 6732
27. S. Chandrasekhar, S.J. Prakash, V. Jagadeshwar, and C. Narsihmulu Tetrahedron Lett. 42 2001 5561 5563
28. B. Kaboudin, and R. Nazari Tetrahedron Lett. 42 2001 8211 8213
29. T. Akiyama, M. Sanada, and K. Fuchibe Synlett 2003 1463 1464
30. J.S. Yadav, B.V.S. Reddy, and C. Madan Synlett 2001 1131 1133
31. R. Gallardo-Macias, and K. Nakayama Synthesis 1 2010 57 62
32. S. Kudrimoti, and R.V. Bommena Tetrahedron Lett. 46 2005 1209 1210
33. S. Ko, and C.F. Yao Tetrahedron Lett. 47 2006 8827 8829
34. A. Tajbakhsh, A. Heydari, H. Alinezhad, M. Ghanei, and S. Khaksarb Synthesis 3 2008 352 354
35. M.M. Kabachnik, L.I. Minaeva, and I.P. Beletskaya Synthesis 14 2009 2357 2360
36. I.L. Odinets, O.I. Artyushin, N. Shevchenko, P.V. Petrovskii, V.G. Nenajdenko, and G.V. Roschenthaler Synthesis 4 2009 577 582
37. S. Sobhani, and A. Vafaee Synthesis 11 2009 1909 1915
38. S. Bhagat, and A.K. Chakraborti J. Org. Chem. 73 2008 6029 6032
39. Q. Chen, and C. Yuan Synthesis 24 2007 3779 3786
40. Q. Chen, J. Li, and C. Yuan Synthesis 18 2008 2986 2990
41. M.B. Thathagar, J. Beckers, and G. Rothenberg J. Am. Chem. Soc. 124 2002 11858 11859
42. M.T. Reetz, and E. Westermann Angew. Chem., Int. Ed. 39 2000 165 168
43. M. Zhao, and R.M. Crooks Angew. Chem., Int. Ed. 38 1999 364 366
44. M.B. Thathagar, J. Beckers, and G. Rothenberg Green Chem. 6 2004 215 218
45. R. Juarez, P. Concepcion, A. Corma, and H. Garcia Chem. Commun. 46 2010 4181 4183
46. B.M. Bhanage, S. Fujita, Y. Ikushima, and M. Arai Appl. Catal., A 219 2001 259 266
47. R. Juarez, A. Corma, and H. Garcia Green Chem. 11 2009 949 952
48. D. Terribile, A. Trovarelli, J. Llorca, C. Leitenburg, and G. Dolcetti J. Catal. 178 1998 299 308
49. S.J. Gregg, J. Rauquerol, and K.S.W. Sing Adsorption at a gas-solid and liquid-solid interface 1982 Elsevier Amsterdam pp 153-164
50. S. Brunauer, L.S. Deming, W.S. Deming, and E. Teller J. Am. Chem. Soc. 62 1940 1723 1732
51. A. Trovarelli Catalysis by Ceria and Related Materials 2 2002 Imperial College Press 409 catalytic science series
52. J. Akbari, and A. Heydari Tetrahedron Lett. 50 2009 4236 4238
53. Z. Karimi-Jaberi, and M. Amiri Heteroat. Chem. 21 2010 96 98
54. S.D. Mitragotri, D.M. Pore, U.V. Desai, and P.P. Wadgaonkar Catal. Commun. 9 2008 1822 1826
55. 2 was characterized with various techniques such as X-ray diffractograms (XRD), Fourier Transform Infra-Red Spectroscopy (FT-IR), Transmission Electron Microscope (TEM), Field Emission Gun-Scanning Electron Microscopes (FEG-SEM) coupled with EDAX and X-ray photoelectron spectroscopy (XPS). See Supplementary data.
56. + 310 (5%).