Bulletin of the Korean Chemical Society

  • 제25권2호
  • /
  • Pages.328-330
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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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Synthesis of 4-Methylene-2-cyclohexenones and Their Aromatization Reaction toward para-Methoxylmethyl Anisole Derivatives

  • Kim, Jeong-Mi (Department of Chemistry and Institute of Basic Science, Chonnam National Univesity) ;
  • Lee, Ka-Young (Department of Chemistry and Institute of Basic Science, Chonnam National Univesity) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National Univesity)
  • 발행 : 2004.02.20
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참고문헌

  1. Kim, J. M.; Lee, K. Y.; Kim, T. H.; Kim, J. N. Bull. KoreanChem. Soc. 2003, 24, 999. https://doi.org/10.5012/bkcs.2003.24.7.999
  2. Kim, J. M.; Lee, K. Y.; Kim, J. N.Bull. Korean Chem. Soc. 2003, 24, 1057. https://doi.org/10.5012/bkcs.2003.24.8.1057
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  5. Basavaiah, D.; Kumaragurubaran, N.; Sharada, D. S. TetrahedronLett. 2001, 42, 85. https://doi.org/10.1016/S0040-4039(00)01886-4
  6. Basavaiah, D.; Rao, A. J.; Satyanarayana, T.Chem. Rev. 2003, 103, 811 https://doi.org/10.1021/cr010043d
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  8. Oikawa, Y.; Nishi, T.; Yonemitsu, O. Tetrahedron Lett.1983, 24, 4037. https://doi.org/10.1016/S0040-4039(00)88256-8
  9. Fellows, I. M.; Kaelin, D. E., Jr.; Martin, S. F.J. Am. Chem. Soc. 2000, 122, 10781. https://doi.org/10.1021/ja0013879
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  11. Silva, C.B.-D.; Pale, P. Tetrahedron: Asymmetry 1998, 9, 3951. https://doi.org/10.1016/S0957-4166(98)00413-3
  12. Oikawa, Y.; Nishi, T.; Yonemitsu, O. J. Chem. Soc., Perkin Trans.1 1985, 7. https://doi.org/10.1039/p19850000007
  13. Davis, B.R.; Johnson, S. J. J. Chem. Soc., Perkin Trans. 1 1979, 2840. https://doi.org/10.1039/p19790002840
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피인용 문헌

  1. Synthesis of 4-Methylene-2-cyclohexenones and Their Aromatization Reaction Toward para-Methoxylmethyl Anisole Derivatives. vol.35, pp.32, 2004, https://doi.org/10.1002/chin.200432105
  2. Molecular Iodine—An Expedient Reagent for Oxidative Aromatization Reactions of α,β-Unsaturated Cyclic Compounds vol.14, pp.12, 2009, https://doi.org/10.3390/molecules14125308
  3. Synthesis of Highly Functionalized 3,4-Dihydro-2H-pyrans from Baylis-Hillman Acetates vol.25, pp.11, 2004, https://doi.org/10.5012/bkcs.2004.25.11.1733
  4. Facile Synthesis of Baylis-Hillman Adducts Bearing the Carbamate or Amide Functional Group at the Secondary Position vol.25, pp.12, 2004, https://doi.org/10.5012/bkcs.2004.25.12.1966
  5. Synthesis of Substituted Cyclopentenes from the Baylis-Hillman Adducts via Ring-Closing Metathesis Reaction vol.25, pp.8, 2004, https://doi.org/10.5012/bkcs.2004.25.8.1280
  6. Baylis-Hillman Reaction and Chemical Transformations of Baylis-Hillman Adducts vol.26, pp.10, 2005, https://doi.org/10.5012/bkcs.2005.26.10.1481
  7. Synthesis of Substituted Uracil Derivatives from the Acetates of the Baylis-Hillman Adducts vol.26, pp.3, 2004, https://doi.org/10.5012/bkcs.2005.26.3.481
  8. Synthesis of Indeno[1,2-b]quinolin-10-ones via Pd/C-Assisted Dehydrogenation of 4b,5,10a,11-Tetrahydroindeno[1,2-b]quinolin-10-ones vol.26, pp.3, 2004, https://doi.org/10.5012/bkcs.2005.26.3.485
  9. Synthesis of Polysubstituted Quinolines from the Acetates of Baylis-Hillman Adducts: Aza-Claisen Rearrangement as the Key Step vol.26, pp.6, 2004, https://doi.org/10.5012/bkcs.2005.26.6.1001
  10. Synthesis of 3-Benzyl- or 3-Benzoyl-7,8-dihydro-6H-chromene Derivatives Starting from Baylis-Hillman Adducts vol.28, pp.1, 2004, https://doi.org/10.5012/bkcs.2007.28.1.147
  11. Advances in the Baylis-Hillman reaction-assisted synthesis of cyclic frameworks vol.64, pp.20, 2008, https://doi.org/10.1016/j.tet.2008.02.087