Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Facile β-Alkylation and β-Hydroxyalkylation of α,β-Unsaturated Lactones and Esters

  • Published : 2002.10.20
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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. Stowell, J. C. Chem. Rev. 1984, 84, 409. https://doi.org/10.1021/cr00063a001
  4. Hoppe, D. Angew. Chem., Int. Ed. Engl. 1984, 23, 932. https://doi.org/10.1002/anie.198409321
  5. Kozikowski, A. P.; Jung, S. H. J. Org. Chem. 1986, 51, 3400. https://doi.org/10.1021/jo00367a040
  6. Kozikowski, A. P.; Jung, S. H. Tetrahedron Lett. 1986, 27, 3227. https://doi.org/10.1016/S0040-4039(00)84760-7
  7. Kim, S.; Lee, P. H. Tetrahedron Lett. 1988, 29, 5413. https://doi.org/10.1016/S0040-4039(00)82882-8
  8. Kim, S.; Lee, P. H.; Kim, S. S. Bull. Korean Chem. Soc. 1989, 10, 218.
  9. Kim, S.; Kim, Y. G.; Park, J. H. Tetrahedron Lett. 1991, 32, 2043. https://doi.org/10.1016/S0040-4039(00)78903-9
  10. Lee, P. H.; Kim, S. Bull. Korean Chem. Soc. 1992, 13, 580.

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