A convenient route to N-perfluoroalkanesulfonyl, N′-phenyldiazene N′-oxide RfSO2N=N+(O) -Ph

Journal of Fluorine Chemistry

Volumn 90, Issue 1, 1998, Pages 59-61

  Xu, Bin ^a   Zhu, Shizheng ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Azoxy compounds; Condensation; N,N dichloroperfluoroalkanesulfonylamines

Indexed keywords

EID: 0032568739     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-1139(98)00157-2     Document Type: Article

References (36)

1. [1] W.H. De Jeu, W.J.A. Goossens, J. Chem. Phys. 61 (1974) 1985.
2. [2] J. Van der Veen, W.H. De deu, M.W.M. Wanninkhof, C.A.M. Tienhoven, J. Phys. Chem. 77 (1973) 2153.
3. [3] A.V. Reiter, V.P. Sevostyanov, O.V. Petrova, Zavod lab. 47 (1981) 20 [CA:94:219079g].
4. [4] T. Muto, Jpn. Kokai Tokkyo Koho Jp. 08,136,914. [CA, 125: 127987g].
5. [5] R.E. MacLeay, US 4,228,069. [CA, 94: 66734q].
6. [6] N. Nishida, A. Kobayashi, T. Nagahama, Bull. Agr. Chem. Soc. Jp. 17 (1955) 77.
7. [7] B. Korsch, N.V. Riggs, Tetrahedron Lett., (1964) 523.
8. [8] C.L. Stevens, B.T. Gillis, T.H. Haskell, J. Am. Chem. Soc. 81 (1959) 1435.
9. [9] W.J. McGahren, M.P. Kunstmann, J. Am. Chem. Soc. 91 (1969) 2808.
10. [10] A. Gasco, A. Serafino, V. Mortarini, E. Menziani, Tetrahedron Lett., (1964) 3431.
11. [11] S.V. Blokhina, G.G. Maidachenko, L.I. Minegv, V.I. Klopov, Zh. Org. Khim. 17 (1) (1981) 151.
12. [12] R.E. Banks, Y. Djebli, R. Fields, N.O. Olawore, R.G. Pritchard, E. Tsiliopoulos, J. Chem. Soc. Perkin Trans I (1989) 1117.
13. [13] S. Oae, T. Fukumoto, M. Yamagami, Bull. Chem. Soc. Jpn. 36 (1963) 728.
14. [14] K. Ohe, S. Uemura, N. Sugita, T. Masuda, J. Org. Chem. 54 (1989) 4169.
15. [15] S.A. Buckler, L. Doll, F.K. Lind, M. Epstein, J. Org. Chem. 27 (1962) 794.
16. [16] B. Baruah, A. Boruah, D. Prajapati, J.S. Sandhu, Chem. Lett. 5 (1996) 351.
17. [17] A. Mckillop, R.A. Raphael, J. Org. Chem. (1970) 1670.
18. [18] Y. Muto, M. Kato, H.B. Jonassen, Bull. Chem. Soc. Jpn. (1967) 1535.
19. [19] Z.M. Hou, Y. Fujwara, H. Taniguchi, J. Org. Chem. 53 (1988) 3118.
20. [20] T.E. Stevens, J. Org. Chem. 32 (1967) 1641.
21. [21] R.A. Moss, T.B.K. Lee, J. Chem. Soc. Perkin I, 1973, 2778.
22. [22] R.M. Moriarty, T.E. Hopkins, I. Prakash, B.K. Vaid, R.K. Vaid, Syn. Comm, 20 (1990) 2353.
23. [23] F.R. Sullivan, E. Luck, P. Kovacic, J. Org. Chem. 39 (1974) 2967.
24. [24] V. Nelson, A. Serianz, P. Kovacic, J. Org. Chem. 41 (1976) 1751.
25. [25] R.C. Zawalski, P. Kovacic, J. Org. Chem. 44 (1979) 2130.
26. [26] O.A. Lauk'yanov, Yu.B. Salamonov, S.I. Zherebyat'ev, et al., Izv. Akad. Nauk, SSSR, Ser. Khim. 5 (1989) 1110.
27. [27] T.E. Stevens, J.P. Freeman, J. Org. Chem. 29 (1964) 2279.
28. [28] R.E. Banks, W.T. Flowers, R.N. Haszeldine, J. Chem. Soc. Perkin Trans I, 1979, 2765.
29. [29] H. Hope, C.B. Shoemaker, D.P. Shoemaker, H.M. Marsden, J.M. Shreeve, J. Org. Chem. 50 (1985) 1136.
30. [30] R.E. Banks, I.M. Farhat, R.R. Fields, G. Pritchard, M.M. Saleh, J. Fluorine Chem. 28 (1985) 325.
31. [31] S.Z. Zhu, J. Chem. Soc. Perkin Trans I, 1994, 2077.
32. [32] S.Z. Zhu, C.M. Zhou, A.W. Li, B. Xu, J. Fluorine Chem. 67 (1994) 7.
33. [33] B. Xu, S.Z. Zhu, Heteroatom Chem. 8 (1997) 309.
34. [34] J.H. Bowie, R.G. Cooks, G.E. Lewis, Aus. J. Chem. 20 (1967) 1601.
35. [35] K.G. Taylor, T. Riehl, J. Am. Chem. Soc. 94 (1972) 250.
36. [36] C.M. Zhou, S.Z. Zhu, Y.H. Zhang, B. Xu, J. Zhang, X.K. Jiang, J. Fluorine Chem. 73 (1995) 175.