Reactions of uracils with trialkyl phosphites and dialkyl phosphonates

Phosphorus, Sulfur and Silicon and Related Elements

Volumn 119, Issue 1-4, 1996, Pages 225-240

  Abdou, Wafaa M ^a   El Khoshnieh, Yehia O ^a   Kamel, Azza A ^a  

^a NATIONAL RESEARCH CENTRE   (Egypt)

Author keywords

Alkyl phosphites; Dithiouracils; Heterocyclic phosphonates; Nitro group deoxygenation by trialkyl phosphites; Uracils

Indexed keywords

EID: 0000384820     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/10426509608043480     Document Type: Article

References (39)

1. K. Issleib, Nachr. Chem. Tech. Lab., 35, 1037, (1987).
2. W. M. Abdou, I. T. Hennawy and Y. O. Elkhoshnieh, J. Chem. Res. (M), 442, (1995).
3. W. M. Abdou, E. M. A. Yakout and N. A. F. Ganoub, Tetrahedron, 51, 411, (1995).
4. W. M. Abdou and N. A. F. Ganoub, J. Heterocyclic Comm., 1, 387, (1995).
5. Y. O. El Khoshnieh, Y. A. Ibrahim and W. M. Abdou, Phosphorus, Sulfur and Silicon, 101, 67, (1995);
6. M. R. Mahran, M. D. Khidre and W. M. Abdou, Phosphorus, Sulfur and Silicon ibid, 101, 17, (1995).
7. W. M. Abdou and N. A. F. Ganoub, Phosphorus, Sulfur and Silicon ibid, 105, 63, (1995).
8. N. G. Kundu, M. Pal and C. Chowdhury, J. Chem. Res., (M), 101, (1995).
9. C. O. Kappe and Th. Kappe, Arch. Pharmaz., 324, 863, (1991).
10. A. Block, Ed. Chemistry, Biology and Clinical Uses of Nucleoside Analogs, Annals of the New York Academy of Sciences, 255, 1, (1975).
11. R. Jeener, C. Harmers-Casterman and N. Mairesse, Biochim. Biophys. Acta, 35, 166, (1959).
12. G. W. Anderson, I. F. Halverstadt, W. H. Miller and R. O. Roblin, Jr., J. Amer. Chem. Soc., 67, 2197, (1945).
13. G. E. Hilbert and T. B. Johnson, J. Amer. Chem. Soc., 52, 2001, (1930);
14. T. B. Johnson and G. E. Helbert, Science, 69, 579, (1929).
15. A. R. Katritzky and A. J. Boulton Ed., Advances in Heterocyclic Chemistry, Academic Press, New York and London, Vol. 8, pp. 15, (1967).
16. R. N. Warrener and E. N. Cain, Chem. Ind. (London), 1989, (1964).
17. R. M. Silverstein, G. C. Bassler, T. C. Morril, Spectroscopic Identification of Organic Compounds, (Wiley Inc., New York, 1981).
18. G. C. Levy, R. L. Lichter and G. L. Nelson (Eds.), Carbon 13 Nuclear Magnetic Resonance Spectroscopy, (John Wiley and Sons, New York, U.S.A. 1980), Chap. 5, p. 135.
19. F. Ramirez, Pure Appl. Chem., 9, 337, (1964).
20. J. J. P. Kokko, L. Mandell and J. H. Goldstein, J. Amer. Chem. Soc., 84, 1042, (1962).
21. S. F. Mason, Recent Work on Naturally Occurring Nitrogen Heterocyclic Compounds, K. Schofield (ed), The Chemical Society, London, 1955 and references therein cited;
22. D. Shugar and J. J. Fox. Bull. Soc. Chim. Belg., 61, 293, (1952).
23. S. Masson, Main Group Chemistry News (MGCN), 2, 18, (1994).
24. (a) F. J. Dinan, H. J. Minnemeyer and H. Tieckelmann, J. Org. Chem., 28, 1015, (1963);
25. (b) H. J. Minnemeyer, J. A. Egyer, J. F. Holland and H. Teikelmann, J. Org. Chem. ibid, 26, 4425, (1961).
26. W. H. Miller, R. O. Roblin and E. B. Astwood, J. Amer Chem. Soc., 67, 2201, (1945).
27. G. Scherowsky and J. Weiland, Chem. Ber., 107, 3155, (1974).
28. E. J. Corey and G. Märkl, Tetrahedron Lett., 3201, (1967).
29. E. A. Arutgunam, V. I. Gunar and S. I. Zav'yalov, Izv. Akad. Nauk SSSR, Ser Khim, (12) 2857, (1969);
30. C.A., 72, 78979, (1970).
31. a) J. I. G. Cadogan, Quart. Rev. Chem. Soc., 16, 208, (1962);
32. b) ibid., Accounts Chem. Res., 5, 303, (1972);
33. c) Y. Maki, T. Hasokami and M. Suzuki, Tetrahedron Lett., 3509, (1971);
34. d) J. I. G. Cadogan, Organophosphorus Reagents in Organic Synthesis, (Academic Press, London, 1979), Chap. 6, pp. 273-283.
35. M. Fieser and L. F. Fieser, Reagents for Organic Synthesis, (John Wiley and Sons, New York, 1975), vol. 4, p 542,
36. M. Fieser and L. F. Fieser, Reagents for Organic Synthesis vol. 5, p. 716.
37. B. C. Sounders, B. P. Stark, Tetrahedron, 4, 197, (1958).
38. C. Hufschmidt, Leibigs Ann., 343, 168, (1905).
39. O. B. Hanover, Leibigs Ann., 385, 314, (1912).