The diverse chemistry of oxazol-5-(4H)-ones

Chemical Society Reviews

Volumn 36, Issue 9, 2007, Pages 1432-1440

  Fisk, Jason S ^a   Mosey, Robert A ^a   Tepe, Jetze J ^a  

^a MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 34547460624     PISSN: 03060012     EISSN: 14604744     Source Type: Journal    
DOI: 10.1039/b511113g     Document Type: Article

References (40)

1. S. L. Schreiber, Science, 2000, 287, 1964.
2. J. Plochl, Ber. Dtsch. Chem. Ges., 1883, 16, 2815.
3. E. Erlenmeyer, Ber. Dtsch. Chem. Ges., 1900, 33, 2036.
4. H. T. Clarke, J. R. Johnson and R. Robinson, The Chemistry of Penicillin, in Oxazoles and Oxazolones, Princeton University Press, Princeton, NJ, 1949, pp. 688–848
5. A. K. Mukerjee, Heterocycles, 1987, 26, 1077.
6. M. Goodman, L. Levine, J. Am. Chem. Soc., 1964, 86, 2918.
7. A. Padwa and W. H. Pearson, Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, 1st edn, 2002, John Wiley and Sons, Hoboken, NJ, pp. 682–747
8. Reported by IUPAC, J. Am. Chem. Soc., 1960, 82, 5545.
9. H. Pellissier, Tetrahedron, 2003, 59, 8291.
10. S. A. Brown, M. C. Parker, N. J. Turner, Tetrahedron: Asymmetry, 2000, 11, 1687.
11. J. Z. Crich, R. Brieva, P. Marquart, R. L. Gu, S. Flemming, C. J. Sih, J. Org. Chem., 1993, 58, 3252.
12. V. Daffe, J. Fastrez, J. Am. Chem. Soc., 1980, 102, 3601.
13. A. Berkessel, S. Mukherjee, F. Cleemann, T. N. Muller, J. Lex, Chem. Commun., 2005, 1898.
14. J. Liang, J. C. Ruble, G. C. Fu, J. Org. Chem., 1998, 63, 3154.
15. G. C. Fu, Acc. Chem. Res., 2000, 33, 412.
16. W. Steglich, G. Hofle, Tetrahedron Lett., 1970, 4727.
17. J. C. Ruble, G. C. Fu, J. Am. Chem. Soc., 1998, 120, 11532.
18. H. V. Nguyen, D. C. D. Butler, C. J. Richards, Org. Lett., 2006, 8, 769.
19. J. G. Seitzberg, C. Dissing, I. Sotofte, P. O. Norrby, M. Johannsen, J. Org. Chem., 2005, 70, 8332.
20. S. A. Shaw, P. Aleman, J. Christy, J. W. Kampf, P. Va, E. Vedejs, J. Am. Chem. Soc., 2006, 128, 925.
21. S. A. Shaw, P. Aleman, E. Vedejs, J. Am. Chem. Soc., 2003, 125, 13368.
22. B. M. Trost, X. Ariza, J. Am. Chem. Soc., 1999, 121, 10727.
23. B. M. Trost, C. Jakel, B. Plietker, J. Am. Chem. Soc., 2003, 125, 4438.
24. X. X. Liu, J. F. Hartwig, Org. Lett., 2003, 5, 1915.
25. J. S. Fisk, J. J. Tepe, J. Am. Chem. Soc., 2007, DOI: 10.1021/ja0627904
26. M. Keni, J. J. Tepe, J. Org. Chem., 2005, 70, 4211.
27. E. Funke, R. Huisgen, Chem. Ber., 1971, 104, 3222.
28. G. Cremonesi, P. Dalla Croce, C. La Rosa, Helv. Chim. Acta, 2005, 88, 1580.
29. R. Huisgen, H. Gotthard, H. O. Bayer, F. C. Schaefer, Chem. Ber., 1970, 103, 2611.
30. F. M. Hershenson, M. R. Pavia, Synthesis, 1988, 999.
31. F. Clerici, M. L. Gelmi, P. Trimarco, Tetrahedron, 1998, 54, 5763.
32. T. Okano, T. Uekawa, N. Morishima, S. Eguchi, J. Org. Chem., 1991, 56, 5259.
33. E. Brunn, E. Funke, H. Gotthard, R. Huisgen, Chem. Ber., 1971, 104, 1562.
34. R. Consonni, P. D. Croce, R. Ferraccioli, C. Larosa, J. Chem. Res. (S), 1991, 188.
35. M. T. Bilodeau, A. M. Cunningham, J. Org. Chem., 1998, 63, 2800.
36. H. Gotthardt, R. Huisgen, F. C. Schaefer, Tetrahedron Lett., 1964, 487.
37. C. A. Maryanoff, C. B. Karash, I. J. Turchi, E. R. Corey, B. E. Maryanoff, J. Org. Chem., 1989, 54, 3790.
38. S. Peddibhotla, J. J. Tepe, J. Am. Chem. Soc., 2004, 126, 12776.
39. S. Peddibhotla, J. J. Tepe, Synthesis, 2003, 1433.
40. V. Sharma, J. I. Tepe, Org. Lett., 2005, 7, 5091.