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Microwave-assisted Kabachnik-Fields Reaction in Ionic Liquid


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References

  1. Welton, T. Chem. Rev. 1999, 99, 2071. https://doi.org/10.1021/cr980032t
  2. Wasserscheid, P.;Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. https://doi.org/10.1002/1521-3773(20001103)39:21<3772::AID-ANIE3772>3.0.CO;2-5
  3. Brown, R.A.; Pollet, P.; McKoon, E.; Eckert, C. A.; Liotta, C. L.; Jessop, P.G. J. Am. Chem. Soc. 2001, 123, 1254. https://doi.org/10.1021/ja005718t
  4. Lee, S.-g.; Park, J. H.; Kang, J.; Lee, J. K. Chem. Commun.2001, 1698.
  5. Song, C. E.; Shim, W. H.; Roh, E. J.; Lee, S.-g.;Choi, J. H. Chem. Commun. 2001, 1122.
  6. Song, C. E.; Oh, C.R.; Roh, E. J.; Choo, D. J. Chem. Commun. 2000, 1743.
  7. Perreux,L.; Loupy, A. Tetrahedron 2001, 57, 9199. https://doi.org/10.1016/S0040-4020(01)00905-X
  8. Lidstrom, P.;Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225. https://doi.org/10.1016/S0040-4020(01)00906-1
  9. Dubreuil, J. F.; Bazureau, J. P. Tetrahedron Lett. 2000, 41,7351. https://doi.org/10.1016/S0040-4039(00)01237-5
  10. Dubreuil, J. F.; Bazureau, J. P. Tetrahedron Lett. 2001,42, 6097. https://doi.org/10.1016/S0040-4039(01)01190-X
  11. Varma, R. S.; Namboodiri, V. V. Pure Appl. Chem.2001, 73, 1309. https://doi.org/10.1351/pac200173081309
  12. Kabachnik, M. J.; Medved, T. Izv. Akad. Nauk SSSR 1954,1126.
  13. Firlds, E. K. J. Am. Chem. Soc. 1952, 74, 1528. https://doi.org/10.1021/ja01126a054
  14. Qian, C.; Huang, T. J. Org. Chem. 1998, 63, 4125. https://doi.org/10.1021/jo971242t
  15. Ranu, B.C.; Hajira, A.; Jana, U. Org. Lett. 1999, 1, 1141. https://doi.org/10.1021/ol990079g
  16. Manabe, K.;Kobayashi, S. Chem. Commun. 2000, 669.
  17. Kaboudin, B.; Nazari,R. Tetrahedron Lett. 2001, 42, 8211. https://doi.org/10.1016/S0040-4039(01)01627-6
  18. Chanderasekhar, S.;Prakash, S. J.; Jagadeshwar, V.; Narsihmulu, C. Tetrahedron Lett.2001, 42, 5561. https://doi.org/10.1016/S0040-4039(01)01053-X

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  25. An Overview of Microwave‐Assisted Kabachnik‐Fields Reactions vol.5, pp.15, 2002, https://doi.org/10.1002/slct.202000693
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