A facile synthesis of α-aminophosphonates catalyzed by ytterbium perfluorooctanoate under solvent-free conditions

Journal of Fluorine Chemistry

Volumn 132, Issue 2, 2011, Pages 102-106

  Tang, Jun ^a   Wang, Limin ^a,b   Wang, Wenbo ^a   Zhang, Liang ^a   Wu, Shengying ^a   Mao, Dan ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Aminophosphonate; Kabacknik Fields reaction; One pot reaction; Ytterbium perfluorooctanoate

Indexed keywords

EID: 79551536466     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2010.12.002     Document Type: Article

References (41)

1. M.C. Allen, W. Fuhrer, B. Tuck, R. Wade, and J.M. Wood J. Med. Chem. 32 1989 1652 1661
2. P.P. Giannousis, and P.A. Bartlett J. Med. Chem. 32 1987 1603 1609
3. F. Allenberger, and I.J. Klare J. Antimicrob. Chemother. 43 1999 211 217
4. P. Kafarski, and B. LeJczak Phosphorus, Sulfur Silicon Relat. Elem. 53 1991 193 215
5. I.A. Natchev Liebigs Ann. Chem. 1988 861 867
6. S.K. Chung, and D.H. Kang Tetrahedron: Asymmetry 7 1996 21 24
7. F.R. Atheron, C.H. Hassal, and R.W. Lambert J. Med. Chem. 29 1986 29 40
8. S. Nakamura, M. Hayashi, Y. Hiramatsu, N. Shibata, Y. Funahashi, and T. Toru J. Am. Chem. Soc. 131 2009 18240 18241
9. X. Zhou, D. Shang, Q. Zhang, L. Lin, X. Liu, and X. Feng Org. Lett. 11 2009 1401 1404
10. J.P. Abell, and H. Yamamoto J. Am. Chem. Soc. 130 2008 10521 10523
11. X. Cheng, R. Goddard, G. Buth, and B. List Angew. Chem. Int. Ed. 47 2008 5079 5081
12. D. Pettersen, M. Marcolini, L. Bernardi, F. Fini, R.P. Herrera, V. Sgarzani, and A. Ricci J. Org. Chem. 71 2006 6269 6272
13. T. Akiyama, H. Morita, J. Itoh, and K. Fuchibe Org. Lett. 7 2005 2583 2585
14. G.D. Joly, and E.N. Jacobsen J. Am. Chem. Soc. 126 2004 4102 4103
15. J. Zon Pol. J. Chem. 55 1981 643 646
16. S. Laschat, and H. Kunz Synthesis 1992 90
17. J.S. Yadav, B.V.S. Reddy, K. Sarita RaJ, K. Bhaskar Reddy, and A.R. Prasad Synthesis 2001 2277
18. J.P. Genet, J. Uziel, M. Port, A.M. Touzin, S. Roland, S. Thorimbert, and S. Tanier Tetrahedron Lett. 7 1997 33 36
19. C.T. Qian, and T. Huang J. Org. Chem. 63 1998 4125 4128
20. J.H. Sang-gi Lee, J. Park, J.K. Kang, and Lee Chem. Commun. 2001 1698 1699
21. H. Firouzabadi, N. Iranpoor, and S. Sobhani Synthesis 2004 2692 2696
22. K. Manabe, and S. Kobayashi Chem. Commun. 2000 669 670
23. A. Heydari, M. Zarei, R. AliJanianzadeh, and H. Tavakol Tetrahedron Lett. 42 2001 3629 3631
24. B. Srikant, and K.C. Asit J. Org. Chem. 73 2008 6029 6031
25. T. Akiyama, M. Sanada, and K. Fuchibe Synlett 2003 1463 1464
26. L.M. Wang, and L. Hu J. Fluorine Chem. 130 2009 406 409
27. L.M. Wang, J.H. Shao, H. Tian, and B. Liu J. Fluorine Chem. 127 2006 97 100
28. L.M. Wang, J.W. Han, H. Tian, and J. Sheng Synlett 2005 337 339
29. L.M. Wang, J.W. Han, J. Sheng, H. Tian, and Z.Y. Fan Catal. Commun. 6 2005 201 204
30. G. Roman Tetrahedron 38 1995 10627 10632
31. M. Yamanaka, and T.J. Hirata J. Org. Chem. 74 2009 3266 3271
32. F.Q. Shi, and B.A. Song Org. Biomol. Chem. 7 2009 1292 1298
33. T. Akiyama, H. Morita, P. Bachu, K. Mori, M. Yamanaka, and T. Hirata Tetrahedron 65 2009 4950 4956
34. R.A. Cherkasov, and V.I. Galkin Russ. Chem. Rev. 67 1998 857 882
35. M.J. Bhanushali, N.S. Nandurkar, S.R. Jagtap, and B.M. Bhanage Synth. Commun. 39 2009 845 859
36. S. Sobhani, and A. Vafaee Synthesis 2009 1909 1915
37. J. Wu, W. Sun, H.G. Xia, and X.Y. Sun Org. Biomol. Chem. 9 2006 1663 1666
38. B. Srikant, and K.C. Asit J. Org. Chem. 72 2007 1263 1270
39. A. Vinu, P. Kalita, V.V. Balasubramanian, H. Oveisi, T. Selvan, A. Mano, M.A. Chari, and B.V. Subba Reddy Tetrahedron Lett. 50 2009 7132 7136
40. B.C. Ranu, A. Hajra, and U. Jana Org. Lett. 8 1999 1141 1143
41. R. Ganzarz Tetrahedron 51 1995 10627 10632