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Facile Synthesis of 3-Alkoxymethyl 2(1H)-Quinolinones from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes


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References

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  1. Facile Synthesis of 3-Substituted and 1,3-Disubstituted Quinolin-2(1H)-ones from 2-Nitrobenzaldehydes vol.65, pp.9, 2005, https://doi.org/10.3987/COM-05-10462
  2. Facile Synthesis of 3-Alkoxymethyl 2(1H)-Quinolinones from the Baylis—Hillman Adducts of 2-Nitrobenzaldehydes. vol.34, pp.12, 2002, https://doi.org/10.1002/chin.200312136
  3. Baylis-Hillman Reaction and Chemical Transformations of Baylis-Hillman Adducts vol.26, pp.10, 2005, https://doi.org/10.5012/bkcs.2005.26.10.1481
  4. Synthesis of Polysubstituted Quinolines from the Acetates of Baylis-Hillman Adducts: Aza-Claisen Rearrangement as the Key Step vol.26, pp.6, 2002, https://doi.org/10.5012/bkcs.2005.26.6.1001
  5. Synthesis of Quinoline N-Oxides from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes: Conjugate Addition of Nitroso Intermediate vol.26, pp.7, 2002, https://doi.org/10.5012/bkcs.2005.26.7.1109
  6. Synthesis of Indoles and Benzisoxazolines from Baylis-Hillman Adducts of 2-Nitrobenzaldehydes vol.28, pp.2, 2002, https://doi.org/10.5012/bkcs.2007.28.2.333
  7. Advances in the Baylis-Hillman reaction-assisted synthesis of cyclic frameworks vol.64, pp.20, 2008, https://doi.org/10.1016/j.tet.2008.02.087