β-Aminophosphonic compounds derived from methyl 1-dimethoxyphosphoryl-2-succinimidocyclohex-3-ene-1-carboxylates

Journal of the Chemical Society. Perkin Transactions 1

Volumn 1, Issue 20, 2001, Pages 2632-2637

  Defacqz, Nathalie ^a   Touillaux, Roland ^a   Cordi, Alex ^b   Marchand Brynaert, Jacqueline ^b  

^a UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

^b INSTITUT DE RECHERCHES SERVIER   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; DERIVATIVES; ORGANIC ACIDS; SYNTHESIS (CHEMICAL);

EPOXIDATION;

AROMATIC COMPOUNDS;

EID: 0034740931     PISSN: 14727781     EISSN: 13645463     Source Type: Journal    
DOI: 10.1039/b105111n     Document Type: Article

References (34)

1. Aminophosphonic and Aminophosphinic Acids, Chemistry and Biological Activity, ed. V. P. Kukhar and H. R. Hudson, John Wiley & Sons, New York, 2000.
2. K. Issleib, A. Balszuweit, H.-J. Richter, W. Tonk Z. Chem. 1983, 23, 434.
3. T. Yokomatsu, T. Murano, K. Suemune, S. Shibuya Tetrahedron 1997, 53, 815.
4. D. Enders, H. Wahl, K. Papadopoulos Liebigs Ann. 1995, 1177.
5. N. Defacqz, B. de Bueger, R. Touillaux, A. Cordi, J. Marchand-Brynaert Synthesis 1999, 1368.
6. N. Defacqz, R. Touillaux, B. Tinant, J.-P. Declercq, D. Peeters, J. Marchand-Brynaert J. Chem. Soc., Perkin Trans. 2 1997, 1965.
7. N. Defacqz, R. Touillaux, J. Marchand-Brynaert J. Chem. Res. (S) 1998, 512.
8. N. Defacqz, R. Touillaux, J. Marchand-Brynaert J. Chem. Res. (M) 1998, 2273.
9. J. Marchand-Brynaert, N. Defacqz, R. Robiette Recent Res. Dev. Org. Chem., in the press.
10. C.A. Zezza, M.B. Smith J. Org. Chem. 1988, 53, 1161.
11. M.F. Semmelhack, J.C. Tomesch, M. Czarny, S. Boettger J. Org. Chem. 1978, 43, 1259.
12. M.S. Dappen, R. Pellicciari, B. Natalini, J.B. Monahan, C. Chiorri, A.A. Cordi J. Med. Chem. 1991, 34, 161.
13. Phosphorus-31 NMR, Principles and Applications, D. G. Gorenstein, Academic Press, Inc., London, 1984.
14. C.E. McKenna, M.T. Higa, N.H. Cheung, M.-C. McKenna Tetrahedron Lett. 1977, 155.
15. G.M. Blackburn, D. Ingleson J. Chem. Soc., Chem. Commun. 1978, 870.
16. N. Galiotti, J. Coste, P. Bedos, P. Jouin Tetrahedron Lett. 1996, 37, 3997.
17. A. Holy Synthesis 1998, 381.
18. D.V. Patel, R.J. Schmidt, S.A. Biller, E.M. Gordon, S.S. Robinson, V. Manne J. Med. Chem. 1995, 38, 2906.
19. P. Krapcho Synthesis 1982, 806.
20. P. Krapcho Synthesis 1982, 893.
21. R. Bodalski, E. Rutkowska-Olma Tetrahedron 1980, 36, 2353.
22. Protective Groups in Organic Synthesis, ed. J. W. Greene, John Wiley & Sons, New York, 1981.
23. T. Kamiya, M. Hashimoto, O. Nakaguchi, T. Oku Tetrahedron 1979, 35, 323.
24. T. Sasaki, K. Minamoto, H. Itoh J. Org. Chem. 1978, 43, 2320.
25. V. Van Rheenen, R.C. Kelly, D.Y. Cha Tetrahedron Lett. 1976, 23, 1973.
26. A.L. Henne, P. Hill J. Am. Chem. Soc. 1943, 65, 752.
27. R.E. Parker, N.S. Isaacs Chem. Rev. 1959, 79, 737.
28. A.A. Cordi and M.L. Vasquez, 1988, EP 0 313 002 A2.
29. A.A. Cordi and M.L. Vasquez, 1993, US 005, 177, 240A.
30. A.A. Cordi and E.T. Sun, 1993, US 005, 252, 563A .
31. Z. Jia, D. Bardford, A.J. Flint, N.K. Tonks Science 1995, 268, 1754.
32. D. Barford Curr. Opin. Struct. Biol. 1995, 5, 728.
33. J.B. Aggen, A.C. Nairn, R. Chamberlin Chem. Biol. 2000, 7, R13.
34. B.J. Goldstein, P.-M. Li, W. Ding, F. Ahmad, W.-R. Zhang Vitam. Horm. (San Diego) 1998, 54, 67.