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Synthetic Studies on Soraphen A: Synthesis of the C1-C9 Hemiketal Segment

  • Park, Se-Hwan (Department of Chemistry, Chungbuk National University) ;
  • Lee, Hyo-Won (Department of Chemistry, Chungbuk National University)
  • 발행 : 2008.08.20

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참고문헌

  1. Bedorf, N.; Schomburg, D.; Gerth, K.; Reichenbach, H.; Höfle, G. Liebigs Ann. Chem. 1993, 1017-1021
  2. Gerth, K.; Reichenbach, H.; Bedorf, N.; Irschik, H.; Hofle, G. J. Antibiotics 1994, 47, 23-31 https://doi.org/10.7164/antibiotics.47.23
  3. GBF mbH and Ciba-Geigy AG, EP 0282455 A3
  4. Shen, Y.; Volrath, S. L.; Weatherly, S. C.; Elich, T. D.; Tong, L. Molecular Cell 2004, 16(6), 881-891
  5. Abel, S.; Faber, D.; Hüter, O.; Giese, B. Angew. Chem., Int. Ed. Engl. 1994, 33, 2466-2468 https://doi.org/10.1002/anie.199424661
  6. Abel, S.; Faber, D.; Hüter, O.; Giese, B. Synthesis 1999, 188-197
  7. Vincent, G.; Mansfield, D. J.; Vors, J.-P.; Ciufolini, M. A. Org. Lett. 2006, 11, 2791-2794
  8. Diaz-Oltra, S.; Murga, J.; Falomir, E.; Carda, M.; Peris, G.; Marco, J. A. J. Org. Chem. 2005, 70, 8130-8139 https://doi.org/10.1021/jo051307p
  9. Lee, H. W.; Kim, Y. J. Bull. Korean Chem. Soc. 1996, 17, 1107-1108
  10. Lee, H. W.; Lee, I.-C.; Kim, Y.-S.; Park, S.-U. Bull. Korean Chem. Soc. 2002, 23, 1197-1198 https://doi.org/10.5012/bkcs.2002.23.9.1197
  11. Park, S. H.; Lee, H. W.; Park, S.-U. Bull. Korean Chem. Soc. 2004, 25, 1613-1614 https://doi.org/10.5012/bkcs.2004.25.11.1613
  12. Gurjar, M. K.; Mainkar, A. S.; Srinivas, P. Tetrahedron Lett. 1995, 36, 5967- 5968
  13. Cao, Y.; Eweas, A. F.; Donaldson, W. A. Tetrahedron Lett. 2002, 43, 7831-7834 https://doi.org/10.1016/S0040-4039(02)01727-6
  14. Loubinoux, B.; Sinnes, J.-L.; O'Sullivan, A. C.; Winkler, T. Helv. Chim. Acta 1995, 78, 122-128 https://doi.org/10.1002/hlca.19950780112
  15. Loubinoux, B.; Sinnes, J.-L.; O'Sullivan, A. C.; Winkler, T. Tetrahedron 1995, 51, 3549-3558 https://doi.org/10.1016/0040-4020(95)00098-S
  16. Loubinoux, B.; Sinnes, J.-L.; O'Sullivan, A. C.; Winkler, T. J. Org. Chem. 1995, 60, 953-959 https://doi.org/10.1021/jo00109a028
  17. Gage, J.; Evans, D. A. Org. Symth. 1990, 68, 83-91 https://doi.org/10.15227/orgsyn.068.0083
  18. Evans, D. A.; Bartoli, J.; Shih, T. L. J. Am. Chem. Soc. 1981, 103, 2127- 2129 https://doi.org/10.1021/ja00398a058
  19. Danda, H.; Hansen, M. M.; Heathcock, C. H. J. Org. Chem. 1990, 55, 173-181 https://doi.org/10.1021/jo00288a029
  20. Evans, D. A.; Black, W. C. J. Am. Chem. Soc. 1993, 115, 4497-4513 https://doi.org/10.1021/ja00064a011
  21. Romo, D.; Johnson, D. D.; Plamondon, L.; Miwa, T.; Schreiber, S. L. J. Org. Chem. 1992, 57, 5060-5063 https://doi.org/10.1021/jo00045a008
  22. Hwang, J. M.; Yeom, S. H.; Jung, K. Y. Bull. Korean Chem. Soc. 2007, 28, 821-826 https://doi.org/10.5012/bkcs.2007.28.5.821
  23. Roush, W. R.; Ando, K.; Power, D. B.; Palkowitz, A. D.; Halterman, R. L. J. Am. Chem. Soc. 1990, 112, 6339-6348 https://doi.org/10.1021/ja00173a023
  24. Roush, W. R.; Ando, K.; Power, D. B.; Palkowitz, A. D. J. Am. Chem. Soc. 1990, 112, 6348-6359 https://doi.org/10.1021/ja00173a024
  25. Roush, W. R.; Hoong, L. K.; Palmer, M. A.; Straub, J. A.; Palkowitz, A. D. J. Org. Chem. 1990, 55, 4117-4126 https://doi.org/10.1021/jo00300a032
  26. Yang, H.-H.; Kim, E.-S.; Yoon, Y. J.; Kang, H.-Y. Bull. Korean Chem. Soc. 2006, 27, 473-474 https://doi.org/10.5012/bkcs.2006.27.4.473
  27. Jones, T. K.; Reamer, R. A.; Desmond, R.; Mills, S. G. J. Am. Chem. Soc. 1990, 112, 2998-3017 https://doi.org/10.1021/ja00164a023
  28. Paik, S. Bull. Korean Chem. Soc. 1999, 20, 217-219 https://doi.org/10.1007/BF02697231
  29. Parikh, J. P.; Doering, W. E. J. Am. Chem. Soc. 1967, 89, 5505- 5507 https://doi.org/10.1021/ja00997a067
  30. Panek, J. S.; Masse, C. E. J. Org. Chem. 1997, 62, 8290- 8291 https://doi.org/10.1021/jo971793j
  31. Gage, J. R.; Evans, D. A. Org. Synth. 1989, 68, 83-91. (b) Evans, D. A.; Britton, T. C.; Ellman, J. A. Tetrahedron Lett. 1987, 28, 6141-6144 https://doi.org/10.1016/S0040-4039(00)61830-0

피인용 문헌

  1. : A Natural Product Analogue That Inhibits Acetyl-CoA Carboxylase vol.4, pp.12, 2013, https://doi.org/10.1021/ml400377p
  2. Asymmetric Total Synthesis of Soraphen A: A Flexible Alkyne Strategy vol.121, pp.30, 2009, https://doi.org/10.1002/ange.200901907
  3. Asymmetric Total Synthesis of Soraphen A: A Flexible Alkyne Strategy vol.48, pp.30, 2009, https://doi.org/10.1002/anie.200901907
  4. ChemInform Abstract: Synthetic Studies on Soraphen A: Synthesis of the C1-C9 Hemiketal Segment. vol.40, pp.1, 2009, https://doi.org/10.1002/chin.200901215
  5. Synthesis and characterization of a BODIPY-labeled derivative of Soraphen A that binds to acetyl-CoA carboxylase vol.19, pp.10, 2008, https://doi.org/10.1016/j.bmcl.2009.03.107
  6. The intriguing chemistry and biology of soraphens vol.36, pp.10, 2019, https://doi.org/10.1039/c9np00008a