Bulletin of the Korean Chemical Society

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Facile β-Sulfenylation of α,β-Unsaturated Lactones and Esters

  • Jung, Sun-Ho (Department of Chemistry, Sungshin Women's University) ;
  • Kim, Jung-Hyun (Department of Chemistry, Sungshin Women's University) ;
  • Kim, Hyun-Ju (Department of Chemistry, Sungshin Women's University)
  • Published : 2004.01.20
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Abstract

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References

  1. Posner, G. H. An Introduction to Synthesis Using Organocopper Reagents; Wiley-Interscience: New York, 1980.
  2. Taylor, R. J. K. Organocopper Reagents; Oxford University Press: Oxford, 1994.
  3. Taylor, R. J. K. Synthesis 1985, 364.
  4. Perlmutter, P. Conjugate Addition Reactions in Organic Synthesis; Pergamon Press: Oxford, 1992.
  5. Hulce, M. Org. React. 1990, 38, 225.
  6. Lipshutz, B. H.; Sengupta, S. Org. React. 1992, 41, 135.
  7. Kozikowski, A. P.; Jung, S. H. J. Org. Chem. 1986, 51, 3400. https://doi.org/10.1021/jo00367a040
  8. Kozikowski, A. P.; Jung, S. H. Tetrahedron Lett. 1986, 27, 3227. https://doi.org/10.1016/S0040-4039(00)84760-7
  9. Kim, S.; Lee, P. H. Tetrahedron Lett. 1988, 29, 5413. https://doi.org/10.1016/S0040-4039(00)82882-8
  10. Kim, S.; Lee, P. H.; Kim, S. S. Bull. Korean Chem. Soc. 1989, 10, 218.
  11. Kim, S.; Kim, Y. G.; Park, J. H. Tetrahedron Lett. 1991, 32, 2043. https://doi.org/10.1016/S0040-4039(00)78903-9
  12. Kim, S.; Park, J. H.; Kim, Y. G.; Lee, J. M. J. Chem. Soc., Chem. Commun. 1993, 1188.
  13. Kim, S.; Lee, B. S.; Park, J. H. Bull. Korean Chem. Soc. 1993, 14, 654.
  14. Lee, P. H.; Kim, S. Bull. Korean Chem. Soc. 1992, 13, 580.
  15. Lee, P. H.; Cho, M.; Han, I.-S.; Kim, S. Tetrahedron Lett. 1999, 40, 6975. https://doi.org/10.1016/S0040-4039(99)01438-0
  16. Jung, S. H.; Kim, J. H. Bull. Korean Chem. Soc. 2002, 23, 365. https://doi.org/10.5012/bkcs.2002.23.3.365
  17. Jung, S. H.; Kim, J. H. Bull. Korean Chem. Soc. 2002, 23, 1375. https://doi.org/10.5012/bkcs.2002.23.10.1375

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  3. Facile β-Alkoxycarbonylation and β-Acylation of α,β-Unsaturated Lactones and Esters via the Phosphoniosilylation Process vol.25, pp.11, 2004, https://doi.org/10.5012/bkcs.2004.25.11.1729
  4. BF3·OEt2-Mediated Ring Opening of Oxetanes with Ylides Derived from the Phosphoniosilylation Products of Enones vol.31, pp.11, 2010, https://doi.org/10.5012/bkcs.2010.31.11.3431
  5. A New Entry to β-Functionalization of Enones: Pentyloxy Group Incorporation in the TBSOTf-Mediated Ring-Opening Reaction of Epoxides with Ylides Derived from the Phosphoniosilylation Products of vol.35, pp.8, 2014, https://doi.org/10.5012/bkcs.2014.35.8.2573