Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Regioselective Synthesis of 3-Amino-4-arylisoxazol-5(4H)-ones

  • Shin, Dong-Won (Bio-Organic Science Division, Korea Research Institute of Chemical Technology) ;
  • ChoiLee, Ihl-Young (Bio-Organic Science Division, Korea Research Institute of Chemical Technology) ;
  • Lim, Hee-Jong (Bio-Organic Science Division, Korea Research Institute of Chemical Technology)
  • Received : 2010.07.26
  • Accepted : 2010.09.14
  • Published : 2010.11.20
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Abstract

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References

  1. Padmavathi, V.; Venkata Subbaiah, D. R. C.; Mahesh, K.; Lakshmi, T. R. Chem. Pharm. Bull. 2007, 55, 1704. https://doi.org/10.1248/cpb.55.1704
  2. Drizin, I.; Altenbach, R. J.; Buckner, S. A.; Whiteaker, K. L.; Scott,V. E.; Darbyshire, J. F.; Jayanti, V.; Henry, R. F.; Coghlan, M. J.;Gopalakrishnan, M.; Carroll, W. A. Bioorg. Med. Chem. 2004,12, 1895. https://doi.org/10.1016/j.bmc.2004.01.038
  3. Tong, Y.; Stewart, K. D.; Thomas, S.; Przytulinska, M.; Johnson,E. F.; Klinghofer, V.; Leverson, J.; McCall, O.; Soni, N. B.; Luo,Y.; Lin, N.-h.; Sowin, T. J.; Giranda, V. L.; Penning, T. D. Bioorg. Med. Chem. Lett. 2008, 18, 5206. https://doi.org/10.1016/j.bmcl.2008.08.079
  4. Jeffery, D.; Prager, R. H.; Turner, D.; Dreimanis, M. Tetrahedron 2002, 58, 9965. https://doi.org/10.1016/S0040-4020(02)01348-0
  5. Khalafy, J.; Setamdideh, D.; Akbari Dilmaghani, K. Molecules 2002, 7, 907. https://doi.org/10.3390/71200907
  6. Zvilichovsky, G.; Gurvich, V.; Shlomo Segev, S. J. Org. Chem. 1995, 60, 5250. https://doi.org/10.1021/jo00121a049
  7. Barbieri, W.; Bernardi, L.; Coda, S.; Palamidessi, G. Tetrahedron 1967, 23, 4395. https://doi.org/10.1016/S0040-4020(01)88837-2
  8. Bauer, L.; Nambury, C. N. V. J. Org. Chem. 1961, 26, 4917. https://doi.org/10.1021/jo01070a034
  9. Buyle, R.; Viehe, H. G. Tetrahedron 1969, 25, 3453. https://doi.org/10.1016/S0040-4020(01)82879-9
  10. Kim, C.-K.; Debellis, F.; Maggiulli, C. A. J. Heterocyclic Chem. 1987, 24, 325. https://doi.org/10.1002/jhet.5570240206
  11. Avalos, M.; Babiano, R.; Cintas, P.; Duran, C. J.; Jimenez, J. L.; Palacios, J. C. Tetrahedron 1995, 29, 8043.
  12. Marchand-Brynaert, J.; Moya-Portuguez, M.; Huber, I.; Ghosez, L. J. Chem. Soc. Chem. Commun. 1983, 818.
  13. Foloppe, M. P.; Rault, S.; Robba, M. Tetrahedron Lett. 1992, 33, 2803. https://doi.org/10.1016/S0040-4039(00)78862-9
  14. Stefan, V.; Kathleen, P.; Muriel, P.; Christophe, B.; Marc, C.; Andrea, V. Helv. Chim. Acta 1999, 82, 963. https://doi.org/10.1002/(SICI)1522-2675(19990707)82:7<963::AID-HLCA963>3.0.CO;2-V
  15. Krpcho, A. P.; Stephens, W. P. J. Org. Chem. 1980, 45, 1106. https://doi.org/10.1021/jo01294a036
  16. Basha, A.; Lipton, M.; Weinreb, S. M. Tetrahedron Lett. 1977, 48, 4171.
  17. Lipton, M.; Basha, A.; Weinreb, S. M. Org. Synth.1979, 59, 49. https://doi.org/10.15227/orgsyn.059.0049
  18. Slider, D. R.; Lovelace, T. C.; MaNamara, J. M.; Reider, P. J. J. Org. Chem. 1994, 59, 1231. https://doi.org/10.1021/jo00085a001
  19. Sim, T. B.; Yoon, N. M. Synlett 1994, 827.

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