Bulletin of the Korean Chemical Society

  • 제35권3호
  • /
  • Pages.699-700
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  • 2014
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Asymmetric Synthesis of Fluoroamines from Chiral Aziridines

  • Park, Hyeonjeong (Department of Chemistry and Protein Research Centre for Bio-Industry, Hankuk University of Foreign Studies) ;
  • Yoon, Doo-Ha (Department of Chemistry and Protein Research Centre for Bio-Industry, Hankuk University of Foreign Studies) ;
  • Ha, Hyun-Joon (Department of Chemistry and Protein Research Centre for Bio-Industry, Hankuk University of Foreign Studies) ;
  • Son, Se In (Department of Chemistry, Sogang University) ;
  • Lee, Won Koo (Department of Chemistry, Sogang University)
  • 투고 : 2013.09.18
  • 심사 : 2013.11.26
  • 발행 : 2014.03.20
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참고문헌

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  2. (b) Chambers, R. D. Fluorine in Organic Chemistry; Blackwell Publishing-CRC Press: Boca Raton, FL, 2004.
  3. (c) Kirsch, P. Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications; Wiley-VCH: Weinheim, 2004.
  4. (d) Hiyama, T. Organofluorine Compounds: Chemistry and Applications; Springer-Verlag: Berlin, 2000.
  5. (a) Ojima, I. Fluorine in Medicinal Chemistry and Chemical Biology; Wiley-Blackwell: Chichester, 2009.
  6. (b) Begue, J.-P.; Bonnet-Delpon, D. J. Fluorine Chem. 2006, 127, 992. https://doi.org/10.1016/j.jfluchem.2006.05.006
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  10. (b) Osborn, H. M. I.; Sweeney, J. B. Tetrahedron: Asymmetry 1997, 8, 1693. https://doi.org/10.1016/S0957-4166(97)00177-8
  11. (c) Zwanenburg, B.; ten Holte, P. In Stereoselective Heterocyclic Chemistry III; Metz, P., Ed.; Springer: Berlin, 2001; pp 93-124.
  12. (d) McCoull, W.; Davis, F. A. Synthesis 2000, 1347.
  13. (e) Sweeney, J. B. Chem. Soc. Rev. 2002, 31, 247. https://doi.org/10.1039/b006015l
  14. (f) Hu, X. E. Tetrahedron 2004, 60, 2701. https://doi.org/10.1016/j.tet.2004.01.042
  15. Stankovic, S.; D'hooghe, M.; Catak, S.; Eum, H.; Waroquier, M.; Van Speybroeck, V.; De Kimpe, N.; Ha, H.-J. Chem. Soc. Rev. 2012, 41, 643. https://doi.org/10.1039/c1cs15140a
  16. (a) Kim, Y.; Ha, H.-J.; Yun, S. Y.; Lee, W. K. Chem. Commun. 2008, 4363.
  17. (b) Yoon, D.-H.; Kang, P.; Lee, W K.; Kim, Y.; Ha, H.-J. Org. Lett. 2012, 14, 429. https://doi.org/10.1021/ol202683k
  18. Kalow, J. A.; Schmitt, D. E.; Doyle, A. G. J. Org. Chem. 2012, 77, 4177. https://doi.org/10.1021/jo300433a
  19. Yook, C.-M.; Eum, H.; Ha, H.-J.; Kang, K. Y.; Lee, W. K. Bull. Korean Chem. Soc. 2011, 32, 2879. https://doi.org/10.5012/bkcs.2011.32.8.2879
  20. (a) D'hooghe, M.; Catak, S.; Stankovic, S.; Waroquier, M.; Kim, Y.; Ha, H.-J.; Van Speybroeck, V.; De Kimpe, N. Eur. J. Org. Chem. 2010, 4920.
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피인용 문헌

  1. F]Fluoride vol.4, pp.1, 2015, https://doi.org/10.1002/open.201402081
  2. Monofluorination of Organic Compounds: 10 Years of Innovation vol.115, pp.17, 2015, https://doi.org/10.1021/cr500706a
  3. ChemInform Abstract: Asymmetric Synthesis of Fluoroamines from Chiral Aziridines. vol.45, pp.36, 2014, https://doi.org/10.1002/chin.201436042
  4. Nucleophilic ring opening reactions of aziridines vol.22, pp.2, 2018, https://doi.org/10.1007/s11030-018-9829-0
  5. Synthesis of Fluorine‐Containing Molecular Entities Through Fluoride Ring Opening of Oxiranes and Aziridines vol.2019, pp.33, 2019, https://doi.org/10.1002/ejoc.201900981
  6. Fluorination -A Decade of Progress (2010-2020) vol.79, pp.10, 2014, https://doi.org/10.5059/yukigoseikyokaishi.79.910