Synthesis of diphenyl α-(dipropoxyphosphoramido)alkyl-phosphonates

Chinese Journal of Chemistry

Volumn 25, Issue 10, 2007, Pages 1551-1554

  Cui, Zhan Wei ^a   Zhang, Jian Feng ^a   Miao, Zhi Wei ^a   Chen, Ru Yu ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

aminoalkanephosphonate; Acetyl chloride; Mannich type reaction; Triphenyl phosphite

Indexed keywords

EID: 36549047112     PISSN: 1001604X     EISSN: None     Source Type: Journal    
DOI: 10.1002/cjoc.200790285     Document Type: Article

References (34)

1. Emsley, J.; Hall, E. D. The Chemistry of Phosphorus, Harper and Row, London, 1976.
2. Kafarski, P.; Lejczak, B. Phosphorus, Sulfur, Silicon Relat Elem. 1991, 63, 193.
3. (a) Hirschmann, R.; Smith, A. B. III.; Taylor, C.; Benkovic, P.; Taylor, S.; Yager, K.; Sprengler, P.; Benkovic, S. Science 1994, 265, 234.
4. (b) Smith, A. B. III.; Taylor, C. M.; Benkovic, J.; Hirtchmann, R. Tetrahedron Lett. 1994, 35, 6853.
5. (a) Allen, M.; Fuhrer, W.; Tuck, B.; Wade, R.; Wood, J. J. Med. Chem. 1989, 32, 1652.
6. (b) Burke, T. R.; Barchi, J. J.; George, C.; Wolf, G.; Shoelson, S. E.; Yan, X. J. Med. Chem. 1995, 38, 1386.
7. Atherton, F.; Hassall, C.; Lambert, R. J. Med. Chem. 1986, 29, 29.
8. (a) Allen, J.; Hassall, C.; Atherton, F.; Hall, M.; HassalL, C.; Holmes, S.; Lambert, R.; Nisbet, L.; Ringrose, P. Nature 1978, 272, 56.
9. (b) Allen, J.; Atherton, F.; Hall, M.; Hassall, C.; Lambert, R.; Nisbet, L.; Ringrose, P. Antimicro. Agents Chemother. 1979, 15, 684.
10. (c) Atherton, F.; Hall, M.; Hassall, C.; Lambert, R.; Ringrose, P. Antimicro. Agents Chemother. 1979, 15, 677.
11. (d) Atherton, F.; Hall, M.; Hassall, C.; Lambert, R.; Lloyd, W.; Ringrose, P. Antimicro. Agents Chemother. 1979, 15, 696.
12. (a) Shuman, C. F.; Vrang, L.; Danielson, U. H. J. Med. Chem. 2004, 47, 5953.
13. (b) Meier, G.; Krause, M.; Huls, A.; Ligneau, X.; Pertz, H. H.; Arrang, J. M.; Ganellin, C. R.; Schwartz, J. C.; Schunack, W.; Stark, H. J. Med. Chem. 2004, 47, 2678.
14. (a) Cruz. A. De. la.; Koeller, K. J.; Rath, N. P.; Spilling, C. D.; Vasconcelos. I. C. F. Tetrahedron 1998, 54, 10513.
15. (b) Zhou, J.; Chen, R. Y.; Yang, X. F. Heteroatom Chem. 1998, 9, 369.
16. (c) Zhou, J.; Chen, R. Y. J. Chem. Soc., Perkin Trans. 1 1998, 2917.
17. (d) Kabachnik, M. M.; Zobnina, E. V.; Beletskaya, I. P. Synlett 2005, 1393.
18. Oleksyszyn, J.; Powers, J. C. Biochemistry 1991, 30, 485.
19. Stroud, R. M.; Kay, L. M.; Dickerson, R. E. J. Mol. Biol. 1974, 83, 185.
20. (a) Oleksyszyn, J.; Tyka, R. Tetrahedron Lett. 1977, 2823.
21. (b) Huber, III, J. W.; Middlebrooks, M. Synthesis 1977, 883.
22. (c) Huber, III, J. W.; Gilmore, W. F. Tetrahedron Lett. 1979, 3049.
23. (d) Oleksyszyn, J.; Subotkowska, L. Synthesis 1980, 906.
24. (e) Tam, C. C.; Mattocks, K.; Tishler, M. Synthesis 1982, 188.
25. Yuan, C. Y.; Chen, S. J.; Wang, G. H. Synthesis 1991, 490.
26. (a) Oleksyszyn, J.; Gruszecha, E. Tetrahedron Lett. 1981, 3537.
27. (b) Yuan, C. Y.; Yuan, Q.; Xie, X. K. Chin. J. Org. Chem. 1989, 9, 136 (in Chinese).
28. (c) Oleksyszyn, J. Synthesis 1981, 444.
29. (a) Yuan, C. Y.; Qi, Y. M. Synthesis 1986, 821.
30. (b) Yuan, C. Y.; Qi, Y. M. Synthesis 1988, 472.
31. (c) Yuan, C. Y.; Wang, G. H.; Chen, S. J. Synthesis 1990, 522.
32. (a) Cherkasov, R. A.; Galkin, V. I. Russ. Chem. Rev. 1998, 67, 857.
33. (b) Miao, Z. W.; Wang, B.; Zhang, G. H.; Chen, R. Y. Bioorg. Chem. 2006, 34, 167.
34. Li, Z. G.; Wang, Q. M.; Huang, J. M. Synthesis of Organic Intermediates, Chemistry Engineering Industry Press, Beijing, 2001, p. 205 (in Chinese).