Bulletin of the Korean Chemical Society

  • 제25권1호
  • /
  • Pages.19-20
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  • 2004
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Aromatization of Hantzsch 1,4-Dihydropyridines with a Polymer-supported Hyervalent Iodine Reagent

  • 발행 : 2004.01.20
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참고문헌

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  5. Ko, K.-Y.; Kim, J.-Y. Tetrahedron Lett.1999, 40, 3207. https://doi.org/10.1016/S0040-4039(99)00467-0
  6. Zolfigol, M. A.; Shirini, F.; Choghamarani, A. G.; Mohammadpoor-Baltork, I. Phosphorus Sulfur and Silicon and the RelatedElements 2003, 178, 1709. https://doi.org/10.1080/10426500307836
  7. Moriarty, R. M.; Vaid, R. K.; Koser, G. F. Synlett 1990, 365.
  8. Koser, G. F. Aldrichimica Acta 2001, 34, 89.
  9. Varvoglis, A. Tetrahedron 1997, 53, 1179. https://doi.org/10.1016/S0040-4020(96)00970-2
  10. Ley, S. V.; Thomas, A. W.; Finch, H. J. Chem. Soc., Perkin Trans.1 1999, 669.
  11. Sakuratani, K.; Togo, H. Synthesis 2003, 21.
  12. Togo, H.;Nogami, G.; Yokoyama, M. Synlett 1998, 534.
  13. Ficht, S.; Mülbaier, M.; Giannis, A. Tetrahedron 2001, 57, 4863. https://doi.org/10.1016/S0040-4020(01)00424-0
  14. Sorg, G.; Mengel, A.; Jung, G.; Rademann, J. Angew. Chem. Int.Ed. 2001, 40, 4395. https://doi.org/10.1002/1521-3773(20011203)40:23<4395::AID-ANIE4395>3.0.CO;2-R

피인용 문헌

  1. Catalytic Aromatization of Hantzsch 1,4-Dihydropyridines by Bis(salicylaldehyde-1,2-phenylenediimine) Mn(III) Chloride Using Urea Hydrogen Peroxide as Mild and Efficient Oxidant vol.65, pp.9, 2005, https://doi.org/10.3987/COM-05-10446
  2. Silica Chromate as a Novel Oxidizing Agent for the Oxidation of 1,4‐Dihydropyridines vol.37, pp.11, 2007, https://doi.org/10.1080/00397910701316276
  3. Aromatization of Hantzsch 1,4-Dihydropyridines with a Polymer-Supported Hypervalent Iodine Reagent. vol.35, pp.32, 2004, https://doi.org/10.1002/chin.200432156
  4. under both heterogeneous and solvent free conditions vol.43, pp.1, 2006, https://doi.org/10.1002/jhet.5570430131
  5. An efficient, metal-free, room temperature aromatization of Hantzsch-1,4-dihydropyridines with urea–hydrogen peroxide adduct, catalyzed by molecular iodine vol.64, pp.24, 2004, https://doi.org/10.1016/j.tet.2008.04.040
  6. Facile and efficient aromatization of 1,4-dihydropyridines with M(NO3)2.XH2O, TNCB, TBAP and HMTAI and preparation of deuterium labeled dehydronifedipine from nifedipi vol.20, pp.12, 2010, https://doi.org/10.1016/j.bmcl.2010.04.096
  7. n-Butyltriphenylphosphonium peroxodisulfate: A cheap and efficient reagent for the aromatization of Hantzsch 1,4-dihydropyridines vol.22, pp.1, 2011, https://doi.org/10.1016/j.cclet.2010.07.022
  8. Iodobenzene diacetate (IBD) catalyzed an quick oxidative aromatization of Hantzsch-1,4-dihydropyridines to pyridines under ultrasonic irradiation vol.19, pp.4, 2004, https://doi.org/10.1016/j.ultsonch.2011.12.021