Functional Group Interconversion of a β-Nitro Group of Phosphorus Compounds and Synthesis of Some Phosphino Sugars

Nippon Kagaku Kaishi

Volumn 1987, Issue 7, 1987, Pages 1207-1213

  Yamashita, Mitsuji ^a   Yamada, Manabu ^a   Sugiura, Motoyuki ^a   Nomoto, Hiroyilki ^a   Oshikawa, Tatsuo ^a  

^a SHIZUOKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 85016533318     PISSN: 03694577     EISSN: None     Source Type: Journal    
DOI: 10.1246/nikkashi.1987.1207     Document Type: Article

References (45)

1. M. J. R. Salton, Annu. Rev. Biochem., 35, 485(1966).
2. S. Inouye, T. Tsuruoka, T. Niida, J. Antibiot. (Tokyo) Ser. A, 19, 288(1966).
3. H. Paulsen, Angew. Chem., 78, 501(1966).
4. H. Yamamoto, S. Inokawa, Adv. Carbohydr. Chem. Biochem., 42, 135(1984).
5. S. Hanessiari, “Total Synthesis of Natural Products : The ‘Chiron’ Approach,” Pergamon Press, Oxford (1983) p. 228.
6. S. Inouye, T. Tsuruoka, T. Ito, T. Niida, Tetrahedron, 24, 2125(1968).
7. U. G. Nayak, R. L. Whistler, J. Org. Chem., 34, 97 (1969).
8. R. Csuk, B. I. Glanzer, J. Chem. Soc. Chem. Commun., 1986, 343.
9. M. Kandatsu, “Biochemistry of Natural C-P Compounds” ed. by T. Hori, M. Horiguchi, A. Hayasri Maruzen, Kyoto (1984) Chapt. 1.
10. M. Horiguchi, M. Kandatsu, Natare, 184, 901(1959
11. D. E. C. Corbridge, “Phosphorus : An Outline of i Chemistry, Biochemistry, and Technology,” Elsvier, Amsterdam (1985) Chapt. 11.
12. R. L. Hilderbrand, J. Curley-Joseph, H. J. Lubansk, T. O. Henderson, “Topics in Phosphorus Chemistry,” ed. by M. Grayson, E.J. Griffith, John Wiley, Ne York (1983) Vol. 11 Chapt. 4.
13. M. Horiguchi, “Biochemistry of Natural C-P Cor pounds”, ed. by T. Hori, M. Horiguchi, A. Hayash Maruzen, Kyoto (1984) Chapt. 6.
14. K. Domroth, “Comprehensive Heterocyclic Chem stry : The Structure, Reactions, Synthesis and Us of Heterocyclic Compounds”, ed. by A. R, Katritzk] Pergamon Press, Oxford (1984) Vol. 1, Chapt. 17.
15. A. J. Kirby, S. G. Warren, “The Chemistry of Phosphorus”, Elsevier, Amsterdam (1967) pp. 37–45.
16. J. I. G. Cadogan, “Organophosphorus Reagents in Organic Synthesis”, ed. by J. I. G. Cadogan, Academic Press, London (1979) Chapt. 1.
17. M. Yamashita, N. Suzuki, M. Yamada, Y. Soeda, H. Yamashita, K. Nakatani, T. Qshikawa, S. Inokawa, Bull. Chem. Soc. Jpn., 56, 219(1983).
18. M. Yamashita, Y. Soeda, N. Suzuki, M. Yamada, K. Tsunekawa, T. Oshikawa, S. Inokawa, Bull. Chem. Soc. Jpn., 56, 1871 (1983).
19. A. J. Kirby, S. G. Warren, “The Chemistry of Phosphorus,” Elsevier, Amsterdam (1967) pp. 45~63.
20. W. E. Nolan, Chem. Rev., 55, 137(1955).
21. H. Shechter, F. T. Williams, Jr., J. Org. Chem., 27, 3699(1962).
22. A. H. Pagano, H. Shechter, J. Org. Chem., 35, 295(1970).
23. J. E. McMurry, J. Melton, H. Padgett, J. Org. Chem., 39, 259 (1974).
24. P. A. Bartlett, F. R. Green, I. D. T. R. Webb, Tetrahedron Lett., 1977, 331.
25. M. R. Galobardes, H. W. Pinniek, Tetrahedron Lett., 1981, 5235.
26. G. A. Olah, B. G. B. Gupta, Synthesis, 1980, 44.
27. E. Keinan, Y. Mazur, J. Am. Chem. Soc., 99, 3861 (1977).
28. N. Kornblum, P. A. Wade, J. Org. Chem., 38, 1418 (1973).
29. J. E. McMurry, J. Melton, J. Am. Chem. Soc., 93, 5309(1971).
30. R. Kirchhoff, Tetrahedron Lett., 1976, 2533.
31. G. A. Olah, B. G. B. Gupta, S. C. Narang, R. Malhotra, J. Org. Chem., 44, 4272(1979).
32. A. H. Haines, “Methods for the Oxidation of Organic Compounds,” Academic Press, London (1985) p. 119.
33. A. P. Schaap, K. A. Zaklika, “Singlet Oxygen,” ed. by H. H. Wasserman, R. W. Murray, Academic Press, New York (1979) Chapt. 6.
34. H. Takayanagi, M. Yamashita, K. Seo, H. Yoshida, T. Ogata, S. Inokawa, Carbohydr. Res., 38, C19 (1974).
35. P. Luger, M. Yamashita, S. Itiokawa, Carbohydr. Res., 84, 25(1980).
36. M. Masui, H. Sayo, J. Pharm. Soc., 4, 332(1956).
37. G. D. Buckley, J. L. Charlish, J. Chem. Soc., 1947. 1472.
38. C. E. Redeman, S. W. Chaikin, R. B. Frearing, J. Am. Chem. Soc., 70. 2582(1948).
39. N. Levy, C. W. Scaife, A. E. W. Smith, J. Chem. Soc., 1948. 52.
40. C. T. Banner, H. T. Kite, J. Am. Chem. Soc., 71, 3598(1949).
41. D. E. Worrall, Org. Synth. Coll. Vol I, 413(1941).
42. United Kingdom Atomic Energy Authority, Fr 1,314,704(1963);
43. Chem. Abstr., 59, 2860b(1963).
44. J. M. GroβSheintz, H. O. L. Fischer, J.Am.Chem Soc., 70, 1476(1948).
45. R. L. Whistler, R. E. Pyler, Carbohydr. Res., 12 201(1970).