Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

An Efficient Synthesis of an Apoptosis Inducer, F-3-2-5 by Using Octanol-Accelerated Baylis-Hillman Reaction

  • Kang, Seock-Yong (Division of Bioscience and Biotechnology, Institute of Biomedical Science and Technology, Konkuk University) ;
  • Park, Kwang-Su (Division of Bioscience and Biotechnology, Institute of Biomedical Science and Technology, Konkuk University) ;
  • Kim, Jin-Young (Division of Bioscience and Biotechnology, Institute of Biomedical Science and Technology, Konkuk University) ;
  • Chong, You-Hoon (Division of Bioscience and Biotechnology, Institute of Biomedical Science and Technology, Konkuk University) ;
  • Choo, Hyun-Ah (Life Sciences Division, Korea Institute of Science and Technology)
  • Published : 2007.02.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Lim, Y.; Lee, C. H.; Kim, B. J.; Moon, S. I.; Lim, H. Y.; Shin, C. S.; Kang, K. L. Novel Inhibitor F-3-2-5 against Cell Cycle Regulating Factor, Preparing Method Thereof and Use for Anti-Cancer Agent. Korea Patent, KP548743, 2006
  2. Gowrisankar, S.; Lee, H. S.; Kim, J. N. Bull. Korean Chem. Soc. 2006, 27, 2097 https://doi.org/10.5012/bkcs.2006.27.12.2097
  3. Cha, M. J.; Song, Y. S.; Lee, K.-J. Bull. Korean Chem. Soc. 2006, 27, 1900 https://doi.org/10.5012/bkcs.2006.27.11.1900
  4. Amri, H. Tetrahedron Lett. 1986, 27, 4307 https://doi.org/10.1016/S0040-4039(00)94260-6
  5. Bode, M. L.; Kaye, P. T. Tetrahedron Lett. 1991, 32, 5611 https://doi.org/10.1016/0040-4039(91)80098-Q
  6. Fort, Y.; Berthe, M. C.; Caubere, P. Tetrahedron 1992, 48, 6371 https://doi.org/10.1016/S0040-4020(01)88227-2
  7. Hoffmann, H. M. R.; Rabe, J. Angew. Chem., Int. Ed. Engl. 1983, 22, 795 https://doi.org/10.1002/anie.198307951
  8. Basavaiah, D.; Gowriswari, V. V. L. Synth. Commun. 1989, 19, 2461 https://doi.org/10.1080/00397918908052648
  9. Kundu, M. K.; Mukherjee, S. B.; Balu, N.; Padmakumar, R.; Bhat, S. V. Synlett 1994, 444
  10. Drewes, S. E.; Roos, G. H. P. Tetrahedron 1988, 44, 4653 https://doi.org/10.1016/S0040-4020(01)86168-8
  11. Basavaiah, D.; Dharma Rao, P.; Suguna Hyma, R. Tetrahedron 1996, 52, 8001 https://doi.org/10.1016/0040-4020(96)00154-8
  12. Kawamura, M.; Kobayashi, S. Tetrahedron Lett. 1999, 40, 1539 https://doi.org/10.1016/S0040-4039(98)02705-1
  13. Ameer, F.; Drewes, S. E.; Freese, S.; Kaye, P. T. Synth. Commun. 1988, 18, 495 https://doi.org/10.1080/00397918808060742
  14. Drewes, S. E.; Freese, S.; Emslie, N. D.; Roos, G. H. P. Synth. Commun. 1988, 18, 1565 https://doi.org/10.1080/00397918808081314
  15. Basavaiah, D.; Sarma, P. K. S. Synth. Commun. 1990, 20, 1611 https://doi.org/10.1080/00397919008053080
  16. Bailey, M.; Marko, I. E.; Ollis, W. D.; Rasmussen, P. R. Tetrahedron Lett. 1990, 31, 4509 https://doi.org/10.1016/S0040-4039(00)97662-7
  17. Auge, J.; Lubin, N.; Lubineau, A. Tetrahedron Lett. 1994, 35, 7947 https://doi.org/10.1016/0040-4039(94)80018-9
  18. Hill, J. S.; Isaacs, N. S. Tetrahedron Lett. 1986, 27, 5007 https://doi.org/10.1016/S0040-4039(00)85119-9
  19. Hill, J. S.; Isaacs, N. S. J. Chem. Res. (S) 1988, 330
  20. Schuurman, R. J. W.; v. d. Linden, A.; Grimbergen, R. P. F.; Nolte, R. J. M.; Scheeren, H. W. Tetrahedron 1996, 52, 8307 https://doi.org/10.1016/0040-4020(96)00384-5
  21. Aggarwal, V. K.; Fulford, S. Y.; Lloyd-Jones, G. C. Angew. Chem. Int. Ed. 2005, 44, 1706 https://doi.org/10.1002/anie.200462462
  22. Chamakh, A.; M'hirsi, M.; Amri, H. Synth. Commun. 1997, 27, 1157 https://doi.org/10.1080/00397919708003352

Cited by

  1. Advances in the Baylis-Hillman reaction-assisted synthesis of cyclic frameworks vol.64, pp.20, 2008, https://doi.org/10.1016/j.tet.2008.02.087