Bulletin of the Korean Chemical Society

  • 제29권6호
  • /
  • Pages.1099-1100
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  • 2008
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  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Facile Synthesis of Aza-Baylis-Hillman Adducts of Cycloalkenones: FeCl3-Mediated Direct Amination of Baylis-Hillman Alcohols

  • Lee, Ka-Young (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Lee, Hyun-Seung (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
  • 발행 : 2008.06.20
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참고문헌

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피인용 문헌

  1. Direct substitution of the hydroxy group with highly functionalized nitrogen nucleophiles catalyzed by Au(iii) vol.47, pp.29, 2011, https://doi.org/10.1039/c1cc12760h
  2. )-Catalyzed tandem reaction of chromone-derived Morita–Baylis–Hillman alcohols with amines vol.9, pp.1, 2011, https://doi.org/10.1039/C0OB00604A
  3. Aluminum Triflate as a Powerful Catalyst for Direct Amination of Alcohols, Including Electron-Withdrawing Group-Substituted Benzhydrols vol.354, pp.13, 2012, https://doi.org/10.1002/adsc.201200536
  4. A direct synthetic route to allyl sulfides from cyclic Morita–Baylis–Hillman alcohols vol.38, pp.2, 2017, https://doi.org/10.1080/17415993.2016.1255742
  5. Transition metal-free direct nucleophilic α-substitution of Morita–Baylis–Hillman alcohols with amines and thiols vol.47, pp.9, 2017, https://doi.org/10.1080/00397911.2017.1295081
  6. -Mediated Direct Amination of Baylis-Hillman Alcohols. vol.39, pp.43, 2008, https://doi.org/10.1002/chin.200843051
  7. Iron(III) chloride-catalysed direct nucleophilic α-substitution of Morita-Baylis-Hillman alcohols with alcohols, arenes, 1,3-dicarbonyl compounds, and thiols vol.7, pp.20, 2009, https://doi.org/10.1039/b908447a
  8. Ultrasound-promoted access to Baylis-Hillman amines vol.16, pp.6, 2008, https://doi.org/10.1016/j.ultsonch.2009.02.006
  9. An Organocatalytic, δ-Regioselective, and Highly Enantioselective Nucleophilic Substitution of Cyclic Morita–Baylis–Hillman Alcohols with Indoles vol.122, pp.40, 2008, https://doi.org/10.1002/ange.201003131
  10. An Organocatalytic, δ-Regioselective, and Highly Enantioselective Nucleophilic Substitution of Cyclic Morita–Baylis–Hillman Alcohols with Indoles vol.49, pp.40, 2008, https://doi.org/10.1002/anie.201003131
  11. Tandem allylic amination/ring-opening/oxa-Michael addition reactions of chromone-derived Morita–Baylis–Hillman acetates with amines vol.67, pp.6, 2008, https://doi.org/10.1016/j.tet.2010.11.089