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A Mild Condition for C-Alkylation of $\beta$-Ketoester

  • Yoo Sung-Eun (Korea Research Institute of Chemical Technology) ;
  • Yi Kyu yang (Korea Research Institute of Chemical Technology)
  • Published : 19890200

Abstract

Keywords

References

  1. Modern Synthetic Reactions(2nd Edition) House, H. O.
  2. Tetrahedron Letters Masamune, S.;Roush, W. R.(et al.)
  3. J. Org. Chem. v.1270 Bottin-Strzalko, T.;Corset, J.;Froment, F.;Ponet, M.-J.;Seyden-Penne, J.;Simonnin, M.-P.
  4. Tetrahedron Letters Howden, M. E. H.;Tyler, M.
  5. Tetrahedron v.34 Cambillau, C.;Bram, G.;Corset, J.
  6. J. Chem. Soc. Chem. Commun. Riche, C.;Pascard-Billy, C.;Cambillau, C.;Bram, C.

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  2. Inherent Oxygen Preference in Enolate Monofluoromethylation and a Synthetic Entry to Monofluoromethyl Ethers vol.123, pp.8, 1989, https://doi.org/10.1002/ange.201006218
  3. Inherent Oxygen Preference in Enolate Monofluoromethylation and a Synthetic Entry to Monofluoromethyl Ethers vol.50, pp.8, 2011, https://doi.org/10.1002/anie.201006218
  4. Cation versus Radical: Studies on the C/O Regioselectivity in Electrophilic Tri-, Di- and Monofluoromethylations of β-Ketoesters vol.1, pp.5, 2012, https://doi.org/10.1002/open.201200032