Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Eschenmoser-Claisen Rearrangement of Baylis-Hillman Adducts

  • Kim, Jeong-Mi (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Sung-Hwan (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
  • Published : 2007.11.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Basavaiah, D.; Pandiaraju, S.; Krishnamacharyulu, M. Synlett 1996, 747-748
  2. Das, B.; Majhi, A.; Reddy, K. R.; Venkateswarlu, K. J. Mol. Catal. A: Chem. 2007, 263, 273-275 https://doi.org/10.1016/j.molcata.2006.08.090
  3. Das, B.; Majhi, A.; Banerjee, J. Tetrahedron Lett. 2006, 47, 7619-7623 https://doi.org/10.1016/j.tetlet.2006.08.060
  4. Chapuis, C.; Buchi, G. H.; Wuest, H. Helv. Chim. Acta 2005, 88, 3069-3088 https://doi.org/10.1002/hlca.200590248
  5. Basavaiah, D.; Pandiaraju, S. Tetrahedron Lett. 1995, 36, 757-758 https://doi.org/10.1016/0040-4039(94)02360-N
  6. Lee, H. J.; Kim, H. S.; Kim, J. N. Tetrahedron Lett. 1999, 40, 4363-4366 https://doi.org/10.1016/S0040-4039(99)00749-2
  7. Lee, H. J.; Chung, Y. M.; Lee, K. Y.; Kim, J. N. Bull. Korean Chem. Soc. 2000, 21, 843-844
  8. Martin Castro, A. M. Chem. Rev. 2004, 104, 2939-3002 https://doi.org/10.1021/cr020703u
  9. Gilbert, M. W.; Galkina, A.; Mulzer, J. Synlett 2004, 2558-2562
  10. Qu, H.; Gu, X.; Min, B. J.; Liu, Z.; Hruby, V. J. Org. Lett. 2006, 8, 4215-4218 https://doi.org/10.1021/ol061414l
  11. Schepens, W.; Haver, D. V.; Vandewalle, M.; Bouillon, R.; Verstuyf, A.; De Clercq, P. J. Org. Lett. 2006, 8, 4247-4250 https://doi.org/10.1021/ol061575p
  12. Loh, T.-P.; Hu, Q.-Y. Org. Lett. 2001, 3, 279-281 https://doi.org/10.1021/ol006918c
  13. Gradl, S. N.; Kennedy-Smoth, J. J.; Kim, J.; Trauner, D. Synlett 2002, 411-414
  14. Kundig, E. P.; Laxmisha, M. S.; Cannas, R.; Tchertchian, S.; Ronggang, L. Helv. Chim. Acta 2005, 88, 1063-1072 https://doi.org/10.1002/hlca.200590078
  15. Hill, R. K.; Soman, R.; Sawada, S. J. Org. Chem. 1972, 37, 3737-3740 https://doi.org/10.1021/jo00796a035
  16. Chen, C.-Y.; Hart, D. J. J. Org. Chem. 1993, 58, 3840-3849 https://doi.org/10.1021/jo00067a015
  17. Kundig, E. P.; Cannas, R.; Laxmisha, M.; Ronggang, L.; Tchertchian, S. J. Am. Chem. Soc. 2003, 125, 5642-5643 https://doi.org/10.1021/ja029957n
  18. Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2004, 25, 413-414 https://doi.org/10.5012/bkcs.2004.25.3.413
  19. Lee, K. Y.; Gong, J. H.; Kim, J. N. Bull. Korean Chem. Soc. 2002, 23, 659-660 https://doi.org/10.5012/bkcs.2002.23.5.659
  20. Lee, K. Y.; Lee, H. S.; Kim, J. N. Tetrahedron Lett. 2007, 48, 2007-2011 https://doi.org/10.1016/j.tetlet.2007.01.062
  21. Lee, K. Y.; Lee, Y. J.; Kim, J. N. Bull. Korean Chem. Soc. 2007, 28, 143-146 https://doi.org/10.5012/bkcs.2007.28.1.143
  22. Gowrisankar, S.; Lee, H. S.; Kim, J. N. Bull. Korean Chem. Soc. 2006, 27, 2097-2100 https://doi.org/10.5012/bkcs.2006.27.12.2097
  23. Lee, K. Y.; Park, D. Y.; Kim, J. N. Bull. Korean Chem. Soc. 2006, 27, 1489-1492 https://doi.org/10.5012/bkcs.2006.27.9.1489

Cited by

  1. ChemInform Abstract: Eschenmoser—Claisen Rearrangement of Baylis—Hillman Adducts. vol.39, pp.12, 2008, https://doi.org/10.1002/chin.200812036
  2. Unprecedented E-stereoselectivity on the sigmatropic Hurd-Claisen rearrangement of Morita-Baylis-Hillman adducts: a joint experimental-theoretical study vol.17, pp.18, 2007, https://doi.org/10.1039/c9ob00533a