Bulletin of the Korean Chemical Society

  • 제28권7호
  • /
  • Pages.1203-1205
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  • 2007
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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A Facile Synthesis of 4-Hydroxycoumarin and 4-Hydroxy-2-quinolone Derivatives

  • Park, Su-Jin (Bio-Organic Science Division, Korea Research Institute of Chemical Technology) ;
  • Lee, Jong-Cheol (Bio-Organic Science Division, Korea Research Institute of Chemical Technology) ;
  • Lee, Kee-In (Bio-Organic Science Division, Korea Research Institute of Chemical Technology)
  • 발행 : 2007.07.20
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참고문헌

  1. Darbarwar, M.; Sundaramurthy, V. Synthesis 1982, 337
  2. Shadbolt, R. S.; Woodward, D. R.; Birchwood, P. J. J. Chem. Soc., Perkin Trans. 1 1976, 1190
  3. van Heerden, P. S.; Bezuidenhoudt, B. C. B.; Ferreira, D. J. Chem. Soc., Perkin Trans. 1 1997, 1141
  4. van Heerden, P. S.; Bezuidenhoudt, B. C. B.; Ferreira, D. Tetrahedron 1997, 53, 6045 https://doi.org/10.1016/S0040-4020(97)00254-8
  5. Jung, J. C.; Kim, J. C.; Park, O. S.; Jang, B. S. Arch. Pharm. Res. 1999, 22, 302 https://doi.org/10.1007/BF02976367
  6. McQuaid, L. A.; Smith, E. C.; Lodge, D.; Pralong, E.; Wikel, J. H.; Calligaro, D. O.; O'Malley, P. J. J. Med. Chem. 1992, 35, 3423 https://doi.org/10.1021/jm00096a019
  7. Kulagowski, J. J.; Baker, R.; Curtis, N. R.; Leeson, P. D.; Mawer, I. M.; Moseley, A. M.; Ridgill, M. P.; Rowley, M.; Stansfield, I.; Foster, A. C.; Grimwood, S.; Hill, R. G.; Kemp, J. A.; Marshall, G. R.; Saywell, K. L.; Tricklebank, M. D. J. Med. Chem. 1994, 37, 1402 https://doi.org/10.1021/jm00036a002
  8. Kim, S. H.; Jung, E. J.; So, E. M.; Shen, C. Z.; Chun, H. J.; Kim, Y. M.; Kim, I. K. Bull. Korean Chem. Soc. 2006, 27, 1329 https://doi.org/10.5012/bkcs.2006.27.9.1329
  9. Roh, S.-G.; Baek, M. S.; Hong, K.-S.; Kim, H. K. Bull. Korean Chem. Soc. 2004, 25, 343 https://doi.org/10.5012/bkcs.2004.25.3.343
  10. Sethna, S.; Phadke, R. Org. React. 1953, 7, 1
  11. Jamkhandi, P. S.; Rajagopal, S. Arch. Pharmaz. 1967, 300, 561 https://doi.org/10.1002/ardp.19673000615
  12. Shah, V. R.; Bose, J. L.; Shah, R. C. J. Org. Chem. 1960, 25, 677 https://doi.org/10.1021/jo01074a630
  13. Bose, J. L.; Shah, R. C.; Shah, V. R. Chemistry and Industry 1960, 623
  14. Zeigler, E.; Wolf, R.; Kappe, J. Monatsch 1965, 96, 418 https://doi.org/10.1007/BF00909449
  15. Shobana, N.; Yeshoda, P.; Shanmugam, P. Tetrahedron 1989, 45, 757 https://doi.org/10.1016/0040-4020(89)80106-1
  16. Jung, J.-C.; Kim, J.-C.; Park, O.-S. Synth. Commun. 2000, 30, 1193
  17. Jung, J.-C.; Jung, Y.-J.; Park, O.-S. Synth. Commun. 2001, 31, 1195
  18. Davidson, D.; Bernhard, S. A. J. Am. Chem. Soc. 1948, 70, 3426 https://doi.org/10.1021/ja01190a060
  19. Junek, H.; Ziegler, E.; Herzog, U.; Kroboth, H. Synthesis 1976, 332
  20. Lmamoto, T.; Kodera, M.; Yokoyama, M. Bull. Chem. Soc. Jpn. 1982, 55, 2303 https://doi.org/10.1246/bcsj.55.2303
  21. Buckle, D. R.; Cantelo, B. C. C.; Smith, H.; Spicer, B. A. J. Med. Chem. 1975, 18, 726 https://doi.org/10.1021/jm00241a017

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