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Hydroalumination of Alkynes with LiAlH$_4$ in the Presence of Cp$_2$TiCl$_2$

  • Lee, Hyung-Soo (Department of Chemical Education, Hyosung Women`s University)
  • Published : 1987.12.20

Abstract

Keywords

References

  1. Chem. Lett. K. Isagawa;K. Tatsumi;Y. Otsuji
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  6. J. Organomet. Chem. v.131 F. Sato;S. Sato;M. Sato
  7. Chem. Lett. K. Isagawa;K. Tatsumi;Y. Otsuji
  8. Tetrahedron v.23 E. F. Magoon;L. H. Slaugh

Cited by

  1. ChemInform Abstract: Hydroalumination of Alkynes with LiAlH4 in the Presence of Cp2TiCl2. vol.19, pp.23, 1987, https://doi.org/10.1002/chin.198823146
  2. Catalysis by metal complexes in organoaluminium synthesis vol.59, pp.12, 1987, https://doi.org/10.1070/rc1990v059n12abeh003584
  3. Zr-Catalyzed Regioselective Hydroalumination of Olefins vol.47, pp.3, 1987, https://doi.org/10.5012/jkcs.2003.47.3.297
  4. Ti-Catalyzed Selective Isomerization of Terminal Mono-substituted Olefins vol.26, pp.3, 1987, https://doi.org/10.5012/bkcs.2005.26.3.461
  5. Hydroalumination of Alkenes and Alkynes with LiAlH4 Catalyzed by [C5(CH3)5]2TiCl2 vol.49, pp.3, 1987, https://doi.org/10.5012/jkcs.2005.49.3.321
  6. Cp2TiCl2 Catalyzed Debromination of gem-Dibromocyclopropanes to Cyclopropanes by LiBH4 vol.49, pp.6, 1987, https://doi.org/10.5012/jkcs.2005.49.6.613
  7. Are Alkyne Reductions Chemo-, Regio-, and Stereoselective Enough To Provide Pure (Z)-Olefins in Polyfunctionalized Bioactive Molecules? vol.113, pp.3, 2013, https://doi.org/10.1021/cr3001753
  8. Cp2TiCl2-catalyzed cis-hydroalumination of propargylic amines with Red-Al: stereoselective synthesis of Z-configured allylic amines vol.51, pp.29, 1987, https://doi.org/10.1039/c5cc00950b