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A Novel Synthesis of Flavanones from 2-Hydroxybenzoic Acids

  • Lee, Jae-In (Department of Chemistry/Plant Resources Research Institute, College of Natural Science, Duksung Women's University) ;
  • Jung, Mi-Gung (Department of Chemistry/Plant Resources Research Institute, College of Natural Science, Duksung Women's University) ;
  • Jung, Hye-Jin (Department of Chemistry/Plant Resources Research Institute, College of Natural Science, Duksung Women's University)
  • Published : 2007.05.20

Abstract

Keywords

References

  1. Harborne, J. B. The Flavonoids; Chapman & Hall: London, U. K., 1994; p 406
  2. Harborne, J. B.; Williams, C. A. Nat. Prod. Rep. 2001, 18, 310 https://doi.org/10.1039/b006257j
  3. Nijveldt, R. J.; Nood, E.; Hoorn, D.; Boelens, P. G.; Norren, K.; Leeuwen, P. Am. J. Clin. Nutr. 2001, 74, 418
  4. Heim, K. E.; Tagliaferro, A. R.; Bobilya, D. J. J. Nutr. Biochem. 2002, 13, 572 https://doi.org/10.1016/S0955-2863(02)00208-5
  5. Bohm, B. A. Introduction to Flavonoids; Harwood Academic Publishers: Amsterdam, Netherlands, 1998; p 243
  6. Harborne, J. B. The Flavonoids; Chapman & Hall: London, U. K., 1994; p 427
  7. Maruyama, K.; Tamanaka, K.; Nishinaga, A.; Inada, A.; Nakanishi, T. Tetrahedron Lett. 1989, 30, 4145 https://doi.org/10.1016/S0040-4039(00)99344-4
  8. Makrandi, J. K.; Bala, S. Synth. Comm. 2000, 30, 3555 https://doi.org/10.1080/00397910008087269
  9. Matsushima, R.; Kageyama, H. J. Chem. Soc. Perkin Trans. II 1985, 743
  10. Bidhendi, G. N.; Bannerjee, N. R. Indian J. Chem. 1989, 28B, 352
  11. Harwood, L. M.; Loftus, G. C.; Oxford, A.; Thomson, C. Synth. Comm. 1990, 20, 649 https://doi.org/10.1080/00397919008052306
  12. Chaturvedi, R.; Patil, P. N.; Mulchandani, N. B. Indian J. Chem. 1992, 31B, 340
  13. Paquette, L. A. Encyclopedia of Reagents for Organic Synthesis; John Wiley & Sons: New York, U. S. A., 1995; p 4172
  14. Dutta, C. P.; Roy, L. P. K. Indian J. Chem. 1975, 13, 425
  15. Moorthy, N. S. H. N.; Singh, R. J.; Singh, H. P.; Gupta, S. D. Chem. Pharm. Bull. 2006, 54, 1384 https://doi.org/10.1248/cpb.54.1384
  16. Patonay, T.; Varma, R. S.; Vass, A.; Levai, A.; Dudas, J. Tetrahedron Lett. 2001, 42, 1403 https://doi.org/10.1016/S0040-4039(00)02264-4
  17. Subramanian, R. S.; Balasubramanian, K. K. J. Chem. Soc., Chem. Comm. 1990, 1469
  18. Thomsen, I.; Torssell, K. B. G. Acta Chem. Scand., Ser. B 1988, 42, 303
  19. Hoshino, Y.; Takeno, N. Bull. Chem. Soc. Jpn. 1986, 59, 2903 https://doi.org/10.1246/bcsj.59.2903
  20. Banerji, A.; Goomer, N. C.; Kalena, G. P. Synth. Comm. 1980, 10, 851 https://doi.org/10.1080/00397918008062768
  21. Kelly, S. E.; Vanderplas, B. C. J. Org. Chem. 1991, 56, 1325 https://doi.org/10.1021/jo00003a081
  22. Banerji, A.; Kalena, G. P. Synth. Comm. 1989, 19, 159 https://doi.org/10.1080/00397918908050965
  23. Lee, J. I.; Son, H. S.; Park, H. Bull. Korean Chem. Soc. 2004, 25, 1945 https://doi.org/10.5012/bkcs.2004.25.12.1945
  24. Einhorn, J.; Einhorn, C.; Luche, J. L. Synth. Comm. 1990, 20, 1105 https://doi.org/10.1080/00397919008052817
  25. Procopiou, P. A.; Brodie, A. C.; Deal, M. J.; Hayman, D. F. Tetrahedron Lett. 1993, 34, 7483 https://doi.org/10.1016/S0040-4039(00)60159-4
  26. Carlock, J. T.; Mack, M. P. Tetrahedron Lett. 1978, 19, 5153 https://doi.org/10.1016/S0040-4039(01)85836-6
  27. Subramanian, R. S.; Balasubramanian, K. K. Synth. Comm. 1989, 19, 1255 https://doi.org/10.1080/00397918908054531
  28. Lee, J. I.; Jung, M. G. Bull. Korean Chem. Soc. 2005, 26, 2044 https://doi.org/10.5012/bkcs.2005.26.12.2044
  29. Kasahara, A.; Izumi, T.; Ooshima, M. Bull. Chem. Soc. Jpn. 1974, 47, 2526 https://doi.org/10.1246/bcsj.47.2526

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