Electrolytic partial fluorination of organic compounds. Part 78: Regioselective anodic fluorination of 2-oxazolidinones

Tetrahedron

Volumn 61, Issue 28, 2005, Pages 6854-6859

  Cao, Yi ^a   Suzuki, Katsutoshi ^a   Tajima, Toshiki ^a   Fuchigami, Toshio ^a  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

2 Oxazolidinone; Electrochemical fluorination; Fluorinated 2 oxazolidinone; Partial fluorination

Indexed keywords

2,4 OXAZOLIDINEDIONE DERIVATIVE; 3 (4 FLUOROPHENOXYCARBONYL) 2 OXAZOLIDINONE; 3 ACETYL 4 FLUORO 2 OXAZOLIDINONE; 3 BENZYLOXAZOLIDINE 2,4 DIONE; 3 FLUOROMETHYLOXAZOLIDINE 2,4 DIONE; 3 MENTHOXYCARBONYL 2 OXAZOLIDINONE; 3 MENTHOXYCARBONYL 4 FLUORO 2 OXAZOLIDINONE; 3 METHOXYCARBONYL 4 FLUORO 2 OXAZOLIDINONE; 3 METHYLOXAZOLIDINE 2,4 DIONE; FLUORINE DERIVATIVE; NITROGEN; OXAZOLIDINE 2,4 DIONE; OXAZOLIDINEDIONE DERIVATIVE; PHENYL GROUP; UNCLASSIFIED DRUG;

ARTICLE; ATOM; ELECTROSTIMULATION; FLUORINATION; PRIORITY JOURNAL; STRUCTURE ANALYSIS;

EID: 20444448033     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.04.057     Document Type: Article

References (29)

1. M.E. Dyen, and D. Swern Chem. Rev. 67 1967 197 236
2. T. Wilson J. Org. Chem. 51 1986 2977 2981
3. S. Cesa, V. Mucciante, and L. Rossi Tetrahedron 55 1999 193 200
4. N. Kudo, M. Taniguchi, S. Furuta, K. Sato, T. Endo, and T. Honma J. Agric. Food Chem. 46 1998 5305 5312
5. L.M. Ednie, M.R. Jacobs, and P.C. Appelbaum J. Antimicrob. Chemother. 50 2002 101 105
6. M.B. Gravestock, D.G. Acton, M.J. Betts, M. Dennis, G. Hatter, A. McGregor, M.L. Swain, R.G. Wilson, L. Woods, and A. Wookey Bioorg. Med. Chem. Lett. 13 2003 4179 4186
7. Haga, T.; Toki, T.; Koyanagi, T.; Okada, H.; Yoshida, K.; Imai, O. EP146748,1984
8. R. Juschke, P. Hasel, and P. Sartori J. Fluorine Chem. 90 1998 77 80
9. T. Fuchigami H. Lund O. Hammerich Organic Electrochemistry 4th ed. 2001 Decker New York 1035 1050
10. T. Fuchigami P.S. Mariano Advances in Electron Transfer Chemistry Vol. 6 1999 JAI CT 41 130
11. T. Fuchigami, M. Tetsu, T. Tajima, and H. Ishii Synlett. 2001 1269 1271
12. K. Suda, K. Hotoda, M. Aoyagi, and T. Takanami J. Chem. Soc., Perkin. Trans. 1 1995 1327 1329
13. M. Hasegawa, H. Ishii, and T. Fuchigami Tetrahedron Lett. 43 2002 1503 1505
14. D. Baba, and T. Fuchigami Tetrahedron Lett. 43 2002 4805 4808
15. M. Sawaguchi, S. Hara, T. Fukuhara, and N. Yoneda Israel J. Chem. 39 1999 151 154
16. B.P. Mundy, and Y. Kim J. Heterocycl. Chem. 19 1982 1221 1222
17. C. Kashima, X.C. Huang, Y. Harada, and A. Hosomi J. Org. Chem. 58 1993 793 794
18. D.M.T. Chan Tetrahedron Lett. 37 1996 9013 9016
19. G.S. Poindexter, D.A. Owens, P.L. Dolan, and E. Woo J. Org. Chem. 57 1992 6257 6265
20. D. Baba, H. Ishii, S. Higashiya, and T. Fuchigami J. Org. Chem. 66 2001 7020 7024
21. P. Carato, S. Yous, D. Sellier, J.H. Poupaert, N. Lebegue, and P. Berthelot Tetrahedron 60 2004 10321 10324
22. S.F. Nelsen, and J.T. Ippoliti J. Am. Chem. Soc. 108 1986 4879 4881
23. W. Xu, and P.S. Mariano J. Am. Chem. Soc. 113 1991 1431 1432
24. V.C. Yoon, and P.S. Mariano Acc. Chem. Res. 25 1992 233 240
25. T. Umemoto, and G. Tomizawa Bull. Chem. Soc. Jpn. 59 1986 3625 3629
26. T. Umemoto, and G. Tomizawa J. Org. Chem. 60 1995 6563 6570
27. V.H. Walliygford, M.A. Thorpe, and R.W. Stoughton J. Am. Chem. Soc. 67 1945 522 523
28. M.A. Spielman J. Am. Chem. Soc. 66 1944 1244 1245
29. M.A. Casadei, S. Cesa, and A. Inesi Tetrahedron 51 1995 5891 5900