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Facile β-Alkoxycarbonylation and β-Acylation of α,β-Unsaturated Lactones and Esters via the Phosphoniosilylation Process

  • Kim, Jung-Hyun (Department of Chemistry, Sungshin Women's University) ;
  • Jung, Sun-Ho (Department of Chemistry, Sungshin Women's University)
  • Published : 2004.11.20

Abstract

Keywords

References

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  1. Facile ?-Alkoxycarbonylation and ?-Acylation of ?,?-Unsaturated Lactones and Esters via the Phosphoniosilylation Process. vol.36, pp.13, 2005, https://doi.org/10.1002/chin.200513049
  2. BF3.OEt2-Assisted Ring Opening of Epoxides with Ylides Derived from the Phosphoniosilylation Products of Enones vol.29, pp.11, 2004, https://doi.org/10.5012/bkcs.2008.29.11.2089
  3. 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
  4. Methodological advances permit the stereocontrolled construction of diverse fully synthetic tetracyclines containing an all-carbon quaternary center at position C5a vol.67, pp.51, 2004, https://doi.org/10.1016/j.tet.2011.09.143
  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