DOI QR코드

DOI QR Code

Dehalogenation of Monohalopyridines Catalyzed by Group 4 Metallocene Reagent


Abstract

Keywords

References

  1. Acc. Chem. Res. v.23 Hites R. A.
  2. Chem. Rev. v.66 Kerr, J. A.
  3. Mol. Struct. Energ. v.3 Smart, B. E.
  4. J. Chem. Soc., Perkin Trans. 1 v.1064 Chambers, R. D.;Lndley, A. A.;Fielding, H. C.;Moilliet, J. S.
  5. Scienct v.271 Burdeniuc, J.;Crabtree, R. H.
  6. Inorganic Chemistry v.271 Principles of Structures and Reactivity(2nd ed.) Huheey, J. E.
  7. Organometallics v.9 Watson, P. L.;Tulip, T. H.;Williams, I.
  8. J. Am. Chem. Soc. v.116 Bennett, B. K.;Harrison, R. G.;Richmond, T. G.
  9. Science v.265 Aizenberg, M.;Milstein, D.
  10. Tetrahedron v.51 Liu, Y.;Schwartz, J.
  11. J. Am. Chem. Soc. v.118 Kiplinger, J. L.;Richmond, T. G.
  12. J. Chem. Soc., Chem. Commun. v.1115 Kiplinger, J. L.;Richmond, T. G.
  13. Chem. Letts. v.1251 Hara, R.;Sun, W.-H.;Nishihara, Y.;Takahashi, T.
  14. Organometallics v.14 Woo, H.-G.;Kim, S. Y.;Han,M. K.;Cho, E. J.;Jung, I. N.
  15. Adv. Organomet. Chem. v.42 Gauvin, F.;Harrod, J. F.;Woo, H.-G.
  16. Chem. Lett. v.457 Woo, H-G.;Song, S.-J.
  17. Bull. Korean Chem. Soc. v.20 Woo, H.-G.;Kim, B.-H.;Song, S.-J.
  18. Inorg. Chem. v.12 Samuel, E.
  19. Organometallics v.1 Wolczanski, P. T.;Bercaw, J. E.
  20. Comprehensive Organometallic Chemistry v.3 Cardin, D. J.;Lappert, M. F.;Raston, C. L.;Riley, P. I.;Wilkinson, G.(ed.);Stone, F. G. A.(ed.);Abel, E. W.(Eds.)
  21. Molecular Sieves Principles of Synthesis and Identificaion Szostak, R.
  22. J. Am. Chem. Soc. v.120 Hagiwara, E.;Fujii, A.;Sodeoka, J.
  23. Angew. Chem. Int. Ed. Engl. v.37 Iida, T.;Yamamoto, N.;Matsunaga, S.;Woo,H.-G.;Shibasaki, M.
  24. J. Am. Chem. Soc. v.113 Aue, D. H.;Webb, H. M.;Davidson, W. R.;Toure, P.;Hopkins, H. P.;Moulik, S. P.;Jahagirdar, D. V.
  25. J. Am. Chem. Soc. v.114 Woo, H.-G.;Walzer, J. F.;Tilley, T. D.
  26. J. Organomet. Chem. v.393 Woo,H.-G.;Tilley, T. D.
  27. Angew. Chem. Int. Ed. Engl. v.37 Hao, L.;Harrod, J. F.;Lebuis, A.-M.;Mu, Y.;Shu, R.;Samuel, E.;Woo, H.-G.
  28. J. Chem. Soc. Chem. Commun. v.2013 Hao, L.;Woo, H.-G.;Lebuis, A.-M.;Samuel, E.;Harrod, J. F.
  29. Organomentallics v.8 Roddick, D. M.;Heyn, R. H.;Tilley, T. D.

Cited by

  1. Reactions of Zirconocene Bis(trimethylsilyl)acetylene Complexes with Fluorinated Pyridines: C–H vs. C–F Bond Activation vol.2005, pp.14, 2000, https://doi.org/10.1002/ejic.200500145
  2. Room-temperature catalytic hydrodefluorination of pentafluoro-pyridine by zirconocene fluoro complexes and diisobutylaluminumhydride vol.261, pp.2, 2000, https://doi.org/10.1016/j.molcata.2006.06.027
  3. Titankatalysierte C-F-Aktivierung von Fluoralkenen vol.122, pp.16, 2000, https://doi.org/10.1002/ange.200907162
  4. Titanium-Catalyzed C–F Activation of Fluoroalkenes vol.49, pp.16, 2000, https://doi.org/10.1002/anie.200907162
  5. Zirconocene Dichloride Catalyzed Hydrodefluorination of C sp 2"math vol.124, pp.50, 2000, https://doi.org/10.1002/ange.201207036
  6. Zirconocene Dichloride Catalyzed Hydrodefluorination of C sp 2"math vol.51, pp.50, 2012, https://doi.org/10.1002/anie.201207036
  7. Titanium‐Catalyzed Vinylic and Allylic CF Bond Activation—Scope, Limitations and Mechanistic Insight vol.18, pp.34, 2000, https://doi.org/10.1002/chem.201201125
  8. Selektive katalytische Hydrodefluorierung als Schlüsselschritt zur Synthese bisher unzugänglicher Aminopyridinderivate vol.125, pp.36, 2013, https://doi.org/10.1002/ange.201301927
  9. Selective Catalytic Hydrodefluorination as a Key Step for the Synthesis of Hitherto Inaccessible Aminopyridine Derivatives vol.52, pp.36, 2013, https://doi.org/10.1002/anie.201301927
  10. Transformation of Trifluorotoluenes Triggered by Titanium(IV) Chloride‐Catalyzed Hydrodefluorination using Hydrosilanes vol.358, pp.1, 2016, https://doi.org/10.1002/adsc.201500920
  11. Structural and Synthetic Insights into Sodium‐Mediated‐Ferration of Fluoroarenes vol.104, pp.12, 2000, https://doi.org/10.1002/hlca.202100206