The behavior of 6-methyl-2-thiouracil towards wittig-horner reagents

Phosphorus, Sulfur and Silicon and Related Elements

Volumn 148, Issue , 1999, Pages 177-187

  Yakout, El Sayed M A ^a   Giurgius, Dalal B ^b   Boulos, L S ^a  

^a NATIONAL RESEARCH CENTRE   (Egypt)

^b Ain Shams University   (Egypt)

Author keywords

6 metnyl 2 thiouracil; The alkylated products; The olefinic compounds; The phosphorane adduct; Wittig Horner reagents

Indexed keywords

EID: 0039132611     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/10426509908037009     Document Type: Article

References (28)

1. N.G. Kundu, M. Pal and C. Chowdhury, J. Chem. Res. (M), 101 (1995).
2. C.O. Kappe and Th. Kappe, Arch. Pharm., 324, 863 (1991).
3. A. Block, Ed. Chemistry, Biology and Clinical use of Nucleoside Analogs, Annals of the New York Academy of Science, 2551 (1975).
4. R. Jeener, C. Harmers-Castenman and N. Mairesse, Biochem. Biophys. Acta, 35, 166 (1959).
5. L.S. Boulos and N.M. Abd El-Rahman, Phosphorus, Sulfur and Silcon, 62, 163 (1991).
6. L.S. Boulos and N.M. Abd El-Rahman, Phosphorus, Sulfur and Silcon, 68, 241 (1992).
7. L.S. Boulos and El-Sayed M.A. Yakout, Phosphorus, Sulfur and Silcon, 84, 35 (1993).
8. L.S. Boulos and M.H.N. Arsanious, Phosphorus, Sulfur and Silicon, 89, 185, 1994.
9. L.S. Boulos, M.H.N. Arsanious and N.K. Eldin, Phosphorus, Sulfur and Silicon, 122, 49 (1997)
10. L.S. Boulos and El-Sayed M.A. Yakout, Heteroatom Chem., 8, 253 (1997).
11. L.S. Boulos and M.H.N. Arsanious, Tetrahedron, 53, 3649 (1997).
12. S. Senda, M. Honda, K. Maeno and H. Fujimura, Chem. Pharm. Bull. (Tokyo), 6, 490 (1958); C.A. 53, 10239e (1959).
13. S. Senda, M. Honda, K. Maeno and H. Fujimura, Chem. Pharm. Bull. (Tokyo), 6, 490 (1958); C.A. 53, 10239e (1959).
14. L. Weinstein, Te-Wen Chang and J.B. Hudson, Antibiotics and Chemotherapy, 7, 443 (1957); C.A. 52, 4834j (1958).
15. L. Weinstein, Te-Wen Chang and J.B. Hudson, Antibiotics and Chemotherapy, 7, 443 (1957); C.A. 52, 4834j (1958).
16. J. Gut, J. Morávek, C. Páráknyi, M. Prystas, J. Skoda and F. Sorm, Collection Czechoslov. Chem. Communs., 24, 2986 (1959); C.A. 54, 4611b (1960).
17. J. Gut, J. Morávek, C. Páráknyi, M. Prystas, J. Skoda and F. Sorm, Collection Czechoslov. Chem. Communs., 24, 2986 (1959); C.A. 54, 4611b (1960).
18. H.J. Bestmann and H.J. Lang, Tetrahedron, 25, 2101-2106 (1969).
19. M. Mercey and P. Toube, J. Chem. Res. Synop., 62, 1987, 13; C.A., 107, 1988, 236149x.
20. M. Mercey and P. Toube, J. Chem. Res. Synop., 62, 1987, 13; C.A., 107, 1988, 236149x.
21. B. Agai et al., Period Poly. Tech. Chem. Eng., 18, 47, 66 (1974).
22. B.C. Saunders and B.P. Stark, Tetrahedron, 4, 187, 1964.
23. L.J. Bellamy, "The Infrared Spectrum of Complex Molecules", John Wiley, New York (1964), p. 311.
24. F. Ramirez, O.P. Madan and S.R. Heller, J. Am. Chem. Soc., 87, (1956), 731.
25. F. Ramirez, O.P. Madan and C.P. Smith, Tetrahedron Lett., 3, 20, 1965.
26. K. Bremer, Ann., 378, 188 (1910).
27. E. Wyrzkiewicz et al., Pol. J. Chem., 52, 1697-98, 1978.
28. G.M. Kosolapoff, "Organophosphorus Compounds", 1st ed., J. Wiley and Sons Inc., New York, Chap. 7 (1950).