Bulletin of the Korean Chemical Society

  • 제28권3호
  • /
  • Pages.481-484
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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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Facile and Efficient Synthesis of ±-Glabridin

  • 발행 : 2007.03.20
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참고문헌

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  2. Mitscher, L. A.; Drake, S.; Gollapudi, S. R.; Harris, J. A.; Shankel, D. M. In Antimutagenesis and Anticarcinogenesis Mechanisms; Shankel, D. M., Hartman, P. E., Kada, T., Hollaender, A., Eds.; Plenum: New York, U. S. A., 1986; p 153
  3. Kent, U. M.; Aviram, M.; Rosenblat, M.; Hollenberg, P. F. Drug Metab. Dispos. 2002, 30, 709 https://doi.org/10.1124/dmd.30.6.709
  4. Vaya, J.; Belinky, P. A.; Aviram, M. Free Radic. Biol. Med. 1997, 23, 302 https://doi.org/10.1016/S0891-5849(97)00089-0
  5. Belinky, P. A.; Aviram, M.; Mahmood, S.; Vaya, J. Biol. Med. 1998, 24, 1419
  6. Tamir, S.; Eizenberg, M.; Somjen, D.; Stern, N.; Shelach, R.; Kaye, A.; Vaya, J. Cancer Research 2000, 60, 5704
  7. Nerya, O.; Vaya, J.; Musa, R.; Izrael, S.; Ben-Arie, R.; Tamir, S. J. Agric. Food Chem. 2003, 51, 1201 https://doi.org/10.1021/jf020935u
  8. Yoo, S.-K.; Kang, H.-K.; Kang, K.-S.; Nahm, K.; You, S. W. WO 2005037815
  9. Different synthetic scheme is recently published independently. Koyakumaru, K.; Ueyama, S. JP 2006008604
  10. Carmack, M. In Organic Reaction; John Wiley & Sons: New York, 1956; Vol. 3, p 83
  11. Bandaranayake, W. M.; Crombie, L.; Whiting, D. A. J. Chem. Soc
  12. Bandaranayake, W. M.; Crombie, L.; Whiting, D. A. J. Chem. Soc. (C) 1971, 811
  13. Nomura, T.; Fukai, T.; Hano, Y.; Tsukamoto, K. Heterocycles 1983, 20, 661 https://doi.org/10.3987/R-1983-04-0661
  14. Omokawa, H.; Yamashita, K. Agric. Biol. Chem. 1974, 38, 1731 https://doi.org/10.1271/bbb1961.38.1731
  15. Jung, D.; Song, J.; Lee, D.; Kim, Y.; Lee, Y.; Hahn, J. Bull. Korean Chem. Soc. 2006, 27, 1493 https://doi.org/10.5012/bkcs.2006.27.9.1493

피인용 문헌

  1. Absolute configuration of naturally occurring glabridin vol.69, pp.11, 2013, https://doi.org/10.1107/S0108270113018842
  2. Isolation of flavonoids from the bark of Entada rheedii Spreng vol.15, pp.4, 2015, https://doi.org/10.1007/s13596-015-0201-y
  3. Facile and Efficient Synthesis of (.+-.)-Glabridin (V) vol.38, pp.29, 2007, https://doi.org/10.1002/chin.200729190
  4. Absolute Configurations of (±)-Glabridin Enantiomers vol.30, pp.2, 2007, https://doi.org/10.5012/bkcs.2009.30.2.415
  5. Discovery and preclinical efficacy of HSG4112, a synthetic structural analog of glabridin, for the treatment of obesity vol.45, pp.1, 2021, https://doi.org/10.1038/s41366-020-00686-1