Bulletin of the Korean Chemical Society

  • 제29권9호
  • /
  • Pages.1835-1838
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  • 2008
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Synthesis of α-Methylene-β-Pyrrole Esters via Organocatalytic Regioselective Allylic Substitutions of Morita-Baylis-Hillman Acetates

  • Kwon, Su-Hyun (Department of Chemistry, Kyungpook National University) ;
  • Cho, Chang-Woo (Department of Chemistry, Kyungpook National University)
  • 발행 : 2008.09.30
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참고문헌

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피인용 문헌

  1. -Allylic Alkylation of Hydrazones with Morita-Baylis-Hillman Carbonates vol.357, pp.2-3, 2014, https://doi.org/10.1002/adsc.201400790
  2. ChemInform Abstract: Synthesis of α-Methylene-β-pyrrole Esters via Organocatalytic Regioselective Allylic Substitutions of Morita-Baylis-Hillman Acetates. vol.40, pp.7, 2009, https://doi.org/10.1002/chin.200907117
  3. SN2’ versus SN2 Reactivity: Control of Regioselectivity in Conversions of Baylis–Hillman Adducts vol.16, pp.4, 2010, https://doi.org/10.1002/chem.200902487
  4. Facile Synthesis of N-Tosyl Aza-Baylis-Hillman Adducts of Acrylamide via a Pd-Catalyzed Hydration of Nitrile to Amide vol.31, pp.3, 2010, https://doi.org/10.5012/bkcs.2010.31.03.700
  5. An Efficient Synthesis of Phospha-Morita-Baylis-Hillman Adducts via Michaelis-Arbuzov Reaction of the DABCO Salt of Morita-Baylis-Hillman Bromide vol.34, pp.1, 2008, https://doi.org/10.5012/bkcs.2013.34.1.133