Bulletin of the Korean Chemical Society

  • 제22권2호
  • /
  • Pages.135-136
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  • 2001
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Synthesis of 4-Hydroxyquinolines from the Baylis-Hillman Adducts of 0-Nitrobenzaldehydes

  • 발행 : 20010200
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초록

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참고문헌

  1. Organic Reactions v.51 Ciganek, E.
  2. Tetrahedron v.44 Drewes, S. E.;Roos, G. H. P.
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  4. Tetrahedron Lett. v.41 Kim, H. S.;Kim, T. Y.;Lee, K. Y.;Chung, Y. M.;Lee, H. J.;Kim, J. N.
  5. Tetrahedron Lett. v.39 Lee, H. J.;Seong, M. R.;Kim, J. N.
  6. Tetrahedron Lett. v.40 Lee. H. J.;Kim, H. S.;Kim, J. N.
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  13. Comprehensive Heterocyclic Chemistry II v.5 Jones, G.;Katrizky, A. R.;Ress, C. W.;Scriven, E. F. V. (Eds.)
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  19. For the photolysis experiments a Raynot photochemical reactor (model RPR-2080, the Southern N. E. Ultraviolet Co.) was used. The built-in monochromatic UV light sources (RUL-250 nm UV lamp) was positioned approximately 17cm from the reaction quartz tube
  20. Org. Lett. v.1 Woodrell, C. D.;Kehayova, P. D.;Jain, A.
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  28. Synthesis v.1 Pillai, V. N. R.
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피인용 문헌

  1. Isatin derivatives are reactive electrophilic components for the Baylis–Hillman reaction vol.43, pp.11, 2001, https://doi.org/10.1016/s0040-4039(02)00160-0
  2. Facile Synthesis of 3-Substituted 2(1H)-Quinolinones from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes vol.23, pp.7, 2001, https://doi.org/10.5012/bkcs.2002.23.7.939
  3. A Double Carbon-Carbon Bond Activation of 8-Quinolinyl Cyclopropyl Ketone by Chlorobis(ethylene)rhodium(I) Dimer vol.24, pp.8, 2001, https://doi.org/10.5012/bkcs.2003.24.8.1059
  4. Synthesis of 3-Substituted Quinolines via Transition-Metal-Catalyzed Reductive Cyclization of o-Nitro Baylis−Hillman Acetates vol.68, pp.16, 2001, https://doi.org/10.1021/jo034447c
  5. Copper‐Catalyzed Aerobic Oxidative Carbocyclization– Ketonization Cascade: Selective Synthesis of Quinolinones vol.355, pp.11, 2013, https://doi.org/10.1002/adsc.201300160