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Facile Synthesis of Baylis-Hillman Adducts Bearing the Carbamate or Amide Functional Group at the Secondary Position

  • Lee, Ka-Young (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Taek-Hyeon (Faculty of Applied Chemistry, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
  • Published : 2004.12.20

Abstract

Keywords

References

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  1. Facile Synthesis of Baylis—Hillman Adducts Bearing the Carbamate or Amide Functional Group at the Secondary Position. vol.36, pp.22, 2005, https://doi.org/10.1002/chin.200522078
  2. Synthesis of Polysubstituted Quinolines from the Acetates of Baylis-Hillman Adducts: Aza-Claisen Rearrangement as the Key Step vol.26, pp.6, 2004, https://doi.org/10.5012/bkcs.2005.26.6.1001
  3. Synthesis of Quinoline N-Oxides from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes: Conjugate Addition of Nitroso Intermediate vol.26, pp.7, 2004, https://doi.org/10.5012/bkcs.2005.26.7.1109
  4. Synthesis of 9-Oxo-9,13b-dihydro-7H-benzo[3,4]azepino[2,1-a]isoindole-6-carboxylic Acid Derivatives from Baylis-Hillman Adducts vol.26, pp.7, 2004, https://doi.org/10.5012/bkcs.2005.26.7.1112
  5. Synthesis of 4-Benzylidene-2,5-dimethyl-3,4-dihydro-2H-pyrrole Derivatives from Baylis-Hillman Adducts and Their Chemical Transformations vol.26, pp.8, 2004, https://doi.org/10.5012/bkcs.2005.26.8.1281