Phosphonylation of sugar derivatives using phosphanylium cation

Heterocyclic Communications

Volumn 2, Issue 1, 1996, Pages 41-45

  Kasaka, Tatsuji ^a   Kyoda, Makoto ^a   Fujimoto, Tetsuya ^a   Ohta, Kazuchika ^a   Yamamoto, Iwao ^a   Kakehi, Akikazu ^a  

^a SHINSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0242597374     PISSN: 07930283     EISSN: None     Source Type: Journal    
DOI: 10.1515/HC.1996.2.1.41     Document Type: Article

References (20)

1. J. Balzarini and E. De Clercq, Adv. Exp. Med. Biol. 309A, 29 (1991).
2. E. De Clercq, Int. J. Immunopharmacol. 13, 91 (1991).
3. E. De Clercq, Biochem. Pharmacol. 42, 963 (1991).
4. P. Miller, Mol. Cell. Biol. (Raven Press Series) 1, 83 (1992).
5. G. M. Blackburn, P. R. Ashton, M. J. Guo, M. Rogers, G. Taylor, A. Guranowski and D. Watts, Heteroatom. Chem. 2, 163 (1991).
6. J. D. Smith, Role Phosphonates Living Syst., Hilderbrand, R. L., Ed. 31 (1983).
7. G. M. Blackburn, Chem. Ind. 5, 134 (1981).
8. T. Klenner, P. Valenzuela-Paz, B. K. Keppler, G. Angres, R. H. Scherf, F. Amelung and D. Schmaehl, Cancer Treat. Rev. 17, 253 (1990).
9. R. E. Hoagland, ACS Sym. Ser. 380, 182 (1988).
10. M. D. Coffey and D. G. Ouimette, Symp. Br. Mycol. Soc. 107 (1989).
11. Raymond S. Gross, Shujaath Mehdi and James R. McCarthy, Teträhedon Letters 34, 7197 (1993).
12. P. A. Frey, Pyridine Nucleotide Coenzymes 2, 461 (1987).
13. S. R. Nahorski, C. I. Ragan and R. A. J. Challiss, TIPS 12, 461 (1991).
14. T. Kasaka, A. Matsumura, M. Kyoda, T. Fujimoto, K. Ohta, I. Yamamoto and A. Kakehi, J. Chem. Soc. Parkin Trans. I. 2867 (1994).
15. S. Fleming, K. M. Lupton and K. Jekot, Inorg. Chem. 11, 2534 (1972); B. E. Maryanoff and R. O. Hutchins, J. Org. Chem. 37, 3475 (1972).
16. S. Fleming, K. M. Lupton and K. Jekot, Inorg. Chem. 11, 2534 (1972); B. E. Maryanoff and R. O. Hutchins, J. Org. Chem. 37, 3475 (1972).
17. A. H. Cowley and R. A. Kemp, Chem. Rev. 1985, 85, 367; C. W. Schultz and R. W. Parry, Inorg. Chem. 15, 3046 (1976).
18. A. H. Cowley and R. A. Kemp, Chem. Rev. 1985, 85, 367; C. W. Schultz and R. W. Parry, Inorg. Chem. 15, 3046 (1976).
19. R.U. Lexieux, E. Frage and K. A. Watanabe, Can. J. Chem. 46, 61 (1968).
20. -1. Totals of 2498 unique reflections were collected at 24±1°C, using the ω-2θ scan technique to a maximum 29 value of 55.0°. Data sets were corrected for Lorentz and polarization effects. Absorption correction was not necessary for the compound. Structure was solved by direct methods using 738 reflections with I>3σ(I). The final residuals were R=0.064 and Rw=0.073.