대한화학회지 (Journal of the Korean Chemical Society)

  • 제47권3호
  • /
  • Pages.297-300
  • /
  • 2003
  • /
  • 1017-2548(pISSN)
  • /
  • 2234-8530(eISSN)
대한화학회 (Korean Chemical Society)
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지르코늄을 촉매로 한 올렌핀의 위치 선택성 수소화 알루미늄 첨가반응

Zr-Catalyzed Regioselective Hydroalumination of Olefins

  • 이형수 (대구가톨릭대학교 화학과) ;
  • 김채은 (대구가톨릭대학교 화학과)
  • Hyung Soo Lee (Department of Chemistry, Catholic University of Daegu) ;
  • Chae Eun Kim (Department of Chemistry, Catholic University of Daegu)
  • 발행 : 2003.06.20
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초록

키워드

참고문헌

  1. Negishi, E. Organometallics in Organic Synthesis; Wileyintersciene:New York, 1980.
  2. Collman, J. P.; Hegedus, L. S.; Norton, J. R.; Finke, R.G. In Principles and Applications of OrganotransitionMetal Chemistry; University Science Book: C.A. 1987.
  3. Brown, H. C. Organic Syntheses via Borane; Wileyinterscience:New York. 1975.
  4. Eisch, J. J. In ComprehensiveOrganometallic Chemistry; Wilkinson, G.;Stone G.; Abel, E. Ed.; Pergamon Press: Oxford, 1982;Vol. 1, pp. 555-682.
  5. Crabtree, R. H.: In The OrganometallicChemistry of the Transition Metals; Wiley-Interscience:New York, 1988; pp. 335-370.
  6. Asao, N. Yamamoto, Y. Bull. Chem. Soc. Jpn. 2000, 73, 1071 https://doi.org/10.1246/bcsj.73.1071
  7. Yun, S. S.; Lee, J.;Lee, S. K. Bull. Korean Chem. Soc. 2001, 22, 623.
  8. Yamasaki, S.; Kanai, M.; Shibasaki, M. J. Am. Chem.Soc. 2001, 123, 1256. https://doi.org/10.1021/ja005794w
  9. Eisch, J. J. In Comprehensive Organic Synthesis; Trost,B. M.; Fleming, I. Ed.; Pergamon Press: Oxford, 1991;Vol. 8.
  10. Sato, F.; Sato, S.; Sato, M. J. Organometal. Chem.1976, 122, C25. https://doi.org/10.1016/S0022-328X(00)80622-1
  11. Isagawa, K.; Tatsumi, K.; Otsuji, Y.Chem. Lett. 1976, 1145.
  12. Sato, F.; Sato, S.; Sato, M.J. Organometal. Chem. 1976, 122, C25. https://doi.org/10.1016/S0022-328X(00)80622-1
  13. Sato, F.;Sato, S.; Sato, M. J. Organometal. Chem. 1977, 131,C26. https://doi.org/10.1016/S0022-328X(00)93419-3
  14. Isagawa, K.; Tatsumi, K.; Otsuji, Y. Chem.Lett. 1977, 1117.
  15. Sato, F.; Tomuro, Y.; Ishikawa, H.;Sato, M. Chem. Lett. 1980, 99.
  16. Sato, F.; Sato, S.; Kodama, H.; Sato, M. J. Organometal.Chem. 1977, 142, 71. https://doi.org/10.1016/S0022-328X(00)91817-5
  17. Le Marechal, J-F.;Ephritikhine, M.; Folcher, G. J. Organometal. Chem.1986, 309, C1. https://doi.org/10.1016/S0022-328X(00)99589-5
  18. Asao, N.; Liu, J.; Sudoh, T.; Yamamoto, Y. J. Chem.Soc., Chem. Commun. 1995, 2405.
  19. Asao, N.; Liu, J.; Sudoh, T.; Yamamoto, Y. J. Org. Chem. 1996, 61, 4568. https://doi.org/10.1021/jo952273w
  20. Asao, N.; Matsukawa, Y.; Yamamoto, Y. J. Chem.Soc., Chem. Commun. 1996, 1513.
  21. Matsukawa, Y.;Asao, N.; Yamamoto, Y. Tetrahedron, 1999, 55, 3779. https://doi.org/10.1016/S0040-4020(98)01183-1
  22. Lee, H. S.; Isagawa, K.; Otsuji, Y. Chem. Lett. 1984, 363.
  23. Lee, H. S.; Isagawa, K.; Toyoda, H.; Otsuji, Y. Chem. Lett. 1984, 673.
  24. Lee, H. S.; Bull. KoreanChem. Soc. 1987, 8, 484.
  25. Lee, H. S.; J. KoreanChem. Soc. 1988, 32, 79.
  26. Lee, H. S.; Kim, I. H. J.Korean Chem. Soc. 1993, 37, 689.
  27. Lee, H. S.; Lee,H. Y. Bull. Korean Chem. Soc. 2000, 21, 451.

피인용 문헌

  1. ZrCl2(η-C5Me5)2-AlHCl2·(THF)2: efficient hydroalumination of terminal alkynes and cross-coupling of the derived alanes vol.49, pp.15, 2013, https://doi.org/10.1039/c2cc37537k
  2. Ti-Catalyzed Selective Isomerization of Terminal Mono-substituted Olefins vol.26, pp.3, 2003, https://doi.org/10.5012/bkcs.2005.26.3.461
  3. Hydroalumination of Alkenes and Alkynes with LiAlH4 Catalyzed by [C5(CH3)5]2TiCl2 vol.49, pp.3, 2003, https://doi.org/10.5012/jkcs.2005.49.3.321
  4. Cp2TiCl2 Catalyzed Debromination of gem-Dibromocyclopropanes to Cyclopropanes by LiBH4 vol.49, pp.6, 2003, https://doi.org/10.5012/jkcs.2005.49.6.613