Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Pd(OAc)2-Catalyzed Isomerization of Acetates of the Baylis-Hillman Adducts

  • Park, Jeong-Beom (Department of Chemical Engineering, Hanyang University) ;
  • Ko, Seung-Ho (Department of Chemical Engineering, Hanyang University) ;
  • Kim, Bong-Gyu (Department of Chemical Engineering, Hanyang University) ;
  • Hong, Wan-Pyo (Department of Chemical Engineering, Hanyang University) ;
  • Lee, Kee-Jung (Department of Chemical Engineering, Hanyang University)
  • Published : 2004.01.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Baylis, A. B.; Hillman, M. E. D. German Patent 2155113, 1972;Chem. Abst. 1972, 77, 34174q.
  2. Drewes, S. E.; Roos, G. H. P. Tetrahedron 1988, 44, 4653. https://doi.org/10.1016/S0040-4020(01)86168-8
  3. Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001. https://doi.org/10.1016/0040-4020(96)00154-8
  4. Ciganek, E. In Organic Reactions; Paquette, L. A., Ed.; Wiley: New York, 1997; Vol. 51, pp 201-350.
  5. Kim, J. N.; Lee, K. Y. Curr. Org. Chem. 2002, 6, 627. https://doi.org/10.2174/1385272023374094
  6. Chung, Y. M.; Lee, H. J.; Hwang, S. S.; Kim, J. N. Bull. Korean Chem. Soc. 2001, 22, 799 and references cited therein.
  7. Lee, H. J.; Kim, T. H.; Kim, J. N. Bull. Korean Chem. Soc. 2001, 22, 1059 and references cited therein.
  8. Basavaiah, D.; Muthukumaran, K.; Sreenivasulu, B. Synthesis2000, 545.
  9. Kim, H. S.; Kim, T. Y.; Lee, K. Y.; Chung, Y. M.; Lee, H. J.; Kim,J. N. Tetrahedron Lett. 2000, 41, 2613. https://doi.org/10.1016/S0040-4039(00)00229-X
  10. Foucaud, A.; El Guemmount, F. Bull. Soc. Chim. Fr. 1989, 403.
  11. Mason, P. H.; Emslie, N. D. Tetrahedron 1994, 50, 12001. https://doi.org/10.1016/S0040-4020(01)89311-X
  12. Shanmugam, P.; Singh, P. R. Synlett 2001, 1314.
  13. Shanmugam, P.; Rajasingh, P. Chem. Lett. 2002, 1212.
  14. Song, Y. S.; Lee, C. H.; Lee, K.-J. J. Heterocyclic Chem. 2003, 40, in press.
  15. Lee, C. H.; Song, Y. S.; Cho, H. I.; Yang, J. W.; Lee, K.-J. J. Heterocyclic Chem. 2003, submitted.
  16. Walker, W. E.; Manyik, R. M.; Atkins, K. E.; Farmer, M. L. Tetrahedron Lett. 1970, 26, 3817.
  17. Tsuji, J.; Murata, Y.; Kato, H.; Tsukahara, Y.; Kinoshita, H.; Kotake, H. Chem. Lett. 1985, 931.
  18. Grieco, P. A.; Takigawa, T.; Bongers, S. L.; Tanaka, H. J. Am. Chem. Soc. 1980, 102, 7587. https://doi.org/10.1021/ja00545a044

Cited by

  1. Using Morita-Baylis-Hillman acetates of 2-azidobenzaldehydes for the synthesis of 2-alkoxy-3-cyanomethylquinolines and alkyl quinoline-3-carboxylates vol.48, pp.4, 2011, https://doi.org/10.1002/jhet.667
  2. Pd(OAc)2-Catalyzed Isomerization of Acetates of the Baylis—Hillman Adducts. vol.35, pp.32, 2004, https://doi.org/10.1002/chin.200432053
  3. Synthesis of Indanones via Intramolecular Heck Reaction of Baylis-Hillman Adducts of 2-Iodobenzaldehyde vol.25, pp.6, 2004, https://doi.org/10.5012/bkcs.2004.25.6.927
  4. Synthesis of Methyl (E)-2-Cyanomethylcinnamates Derived from Baylis-Hillman Acetates and Conversion into Several 4-Hydroxy-2-naphthoic Acids and Benzylidenesuccinimides vol.26, pp.4, 2004, https://doi.org/10.5012/bkcs.2005.26.4.655
  5. Synthesis of Symmetric Diallyl Disulfides from Baylis-Hillman Acetates vol.27, pp.11, 2004, https://doi.org/10.5012/bkcs.2006.27.11.1900
  6. Application of the acetate of baylis‐hillman adducts in the synthesis of 3‐carbomethoxy‐2H‐thiochromenes vol.45, pp.1, 2004, https://doi.org/10.1002/jhet.5570450129
  7. Synthesis of β-Aryl Substituted N-Tosyl Aza-Baylis-Hillman Adducts: Heck Reaction of N-Tosyl Aza-Baylis-Hillman Adducts vol.29, pp.8, 2004, https://doi.org/10.5012/bkcs.2008.29.8.1583
  8. Mild and Efficient Palladium Catalyzed Isomerization of Baylis-Hillman Acetates vol.30, pp.5, 2009, https://doi.org/10.5012/bkcs.2009.30.5.1195
  9. Recent advances in the Pd-catalyzed chemical transformations of Baylis-Hillman adducts vol.65, pp.43, 2009, https://doi.org/10.1016/j.tet.2009.07.034
  10. Quinolines from Morita–Baylis–Hillman acetates of 2-azidobenzaldehydes vol.65, pp.46, 2004, https://doi.org/10.1016/j.tet.2009.09.047
  11. Synthesis of (+)-perillyl alcohol from (+)-limonene vol.55, pp.8, 2004, https://doi.org/10.1016/j.tetlet.2014.01.039
  12. Synthesis of tetrahydrothiopyrano[2,3-b]indoles via [3+3] annulation of nitroallylic acetates with indoline-2-thiones vol.44, pp.4, 2004, https://doi.org/10.1039/c9nj04754a