Bulletin of the Korean Chemical Society

  • 제25권12호
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  • Pages.1966-1968
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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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Facile Synthesis of Baylis-Hillman Adducts Bearing the Carbamate or Amide Functional Group at the Secondary Position

  • Lee, Ka-Young (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Taek-Hyeon (Faculty of Applied Chemistry, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
  • 발행 : 2004.12.20
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참고문헌

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  2. Kim, J. M.; Im, Y. J.; Kim, T. H.; Kim, J. N. Bull. Korean Chem.Soc. 2002, 23, 657. https://doi.org/10.5012/bkcs.2002.23.5.657
  3. Gong, J. H.; Kim, H. R.; Ryu, E. K.; Kim,J. N. Bull. Korean Chem. Soc. 2002, 23, 789. https://doi.org/10.1007/BF02705929
  4. Kim, J. N.; Lee,H. J.; Gong, J. H. Tetrahedron Lett. 2002, 43, 9141. https://doi.org/10.1016/S0040-4039(02)02274-8
  5. Kim, J. N.; Lee, H. J.; Kee, K. Y.; Gong, J. H. Synlett 2001, 173.
  6. Chung, Y. M.; Gong, J. H.; Kim, T. H.; Kim, J. N. Tetrahedron Lett. 2001, 42, 9023. https://doi.org/10.1016/S0040-4039(01)01971-2
  7. Kim, J. M.; Lee, K. Y.; Lee, S.-K.; Kim, J. N. Tetrahedron Lett. 2004, 45, 2805. https://doi.org/10.1016/j.tetlet.2004.02.047
  8. Kim, J. M.; Lee, K. Y.; Kim,J. N. Bull. Korean Chem. Soc. 2004, 25, 328. https://doi.org/10.5012/bkcs.2004.25.2.328
  9. Saxena, R.; Patra, A.; Batra, S. Synlett 2003,1439.
  10. Basavaiah, D.; Kumaragurubaran, N. Tetrahedron Lett.2001, 42, 477. https://doi.org/10.1016/S0040-4039(00)01967-5
  11. Basavaiah, D.; Kumaragurubaran, N.; Sharada,D. S. Tetrahedron Lett. 2001, 42, 85. https://doi.org/10.1016/S0040-4039(00)01886-4
  12. Drewes, S. E.; Horn, M.M.; Ramesar, N. Synth. Commun. 2000, 30, 1045. https://doi.org/10.1080/00397910008087122
  13. Basavaiah,D.; Sharada, D. S.; Kumaragurubaran, N.; Reddy, R. M. J. Org.Chem. 2002, 67, 7135. https://doi.org/10.1021/jo0257952
  14. Basavaiah, D.; Kumaragurubaran, N.;Sharada, D. S.; Reddy, R. M. Tetrahedron 2001, 57, 8167. https://doi.org/10.1016/S0040-4020(01)00786-4
  15. Gasperi, T.; Loreto,M. A.; Tardella, P. A.; Gambacorta, A. Tetrahedron Lett. 2002, 43,3017. https://doi.org/10.1016/S0040-4039(02)00390-8
  16. Yamamoto, K.; Takagi, M.; Tsuji, J. Bull. Chem. Soc.Jpn. 1988, 61, 319. https://doi.org/10.1246/bcsj.61.319
  17. Takagi, M.; Yamamoto, K. Tetrahedron1991, 47, 8869. https://doi.org/10.1016/S0040-4020(01)81001-2
  18. Mamaghani, M.; Badrian, A. TetrahedronLett. 2004, 45, 1547. https://doi.org/10.1016/j.tetlet.2003.12.046
  19. Shi, M.; Zhao, G.-L. Tetrahedron Lett.2002, 43, 9171. https://doi.org/10.1016/S0040-4039(02)02263-3
  20. Shi, M.; Zhao, G.-L. Tetrahedron Lett. 2002,43, 4499. https://doi.org/10.1016/S0040-4039(02)00813-4
  21. Tetrahedron Lett. v.42 Basavaiah, D.;Kumaragurubaran, N. https://doi.org/10.1016/S0040-4039(00)01967-5
  22. Tetrahedron Lett. v.45 Shi, M.;Zhao, G.L. https://doi.org/10.1016/j.tetlet.2003.12.046

피인용 문헌

  1. Facile Synthesis of Baylis—Hillman Adducts Bearing the Carbamate or Amide Functional Group at the Secondary Position. vol.36, pp.22, 2005, https://doi.org/10.1002/chin.200522078
  2. 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
  3. Synthesis of Quinoline N-Oxides from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes: Conjugate Addition of Nitroso Intermediate vol.26, pp.7, 2004, https://doi.org/10.5012/bkcs.2005.26.7.1109
  4. Synthesis of 9-Oxo-9,13b-dihydro-7H-benzo[3,4]azepino[2,1-a]isoindole-6-carboxylic Acid Derivatives from Baylis-Hillman Adducts vol.26, pp.7, 2004, https://doi.org/10.5012/bkcs.2005.26.7.1112
  5. Synthesis of 4-Benzylidene-2,5-dimethyl-3,4-dihydro-2H-pyrrole Derivatives from Baylis-Hillman Adducts and Their Chemical Transformations vol.26, pp.8, 2004, https://doi.org/10.5012/bkcs.2005.26.8.1281