Bulletin of the Korean Chemical Society

  • 제8권4호
  • /
  • Pages.350-351
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  • 1987
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Resonance Shunt' Phenomenon in Nucleophilic Substitution of $\alpha$-Carbonyl Derivatives Demonstrated by the Cross Interaction Constants

  • 발행 : 1987.08.20
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참고문헌

  1. Nouv. J. Chim. v.2 S. Wolfe;D. Kost
  2. Tetrahedron Lett. v.23 D. Kost;K. Aviram
  3. Can. J. Chem. v.60 S. Wolfe;D. J. Mitchell;H. B. Schlegel
  4. J. Am. Chem. Soc. v.105 S. S. Shaik
  5. J. Am. Chem. Soc. v.46 J. B. Conant;W. R. Kirner
  6. J. Am. Chem. Soc. v.47 J. B. Conant;W. R. Kirner;R. E. Hussey
  7. J. Chem. Soc. Chem. Commun. A. Halvorsen;J. Songstad
  8. Can. J. Chem. v.51 J. W. Thorpe;J. Warkentin
  9. J. Am. Chem. Soc. v.86 F. G. Bordwell;W. T. Brannen
  10. J. Chem. Soc., Perkin v.2 D. J. McLennan;A. Pross
  11. The Electronic Theory of Organic Chemistry M. J. S. Dewar
  12. J. Am. Chem. Soc. v.73 S. Winstein;E. Grunwald;H. W. Jones
  13. Solvolytic Displacement Reactions A. Streitwieser
  14. J. Chem. Soc. Chem. Commun. I. Lee;S. C. Sohn
  15. I. Lee
  16. I. Lee;H. Y. Kim;H. K. Kang
  17. Tetrahedron Lett. I. Lee;H. K. Kang
  18. Correlation Analysis of Organic Reactivity J. Shorter
  19. I. Lee;K. R. Han
  20. J. Chem. Soc. (B) J. Banger;A. E. Cockrill;G. L. O. Davies
  21. Ph. D. thesis, Inha University H. K. Kang
  22. Tetrahedron v.39 I. Lee;I. S. Koo
  23. J. Org. Chem. v.41 F. P. Ballistreri;E. Maccarone;A. Mamo
  24. J. Am. Chem. Soc. v.96 G. M. Loudin;C. Berke
  25. J. Am. Chem. Soc. v.106 J. P. Richard;M. E. Rothenberg;W. P. Jencks
  26. tetrahedron Lett. v.23 H. Yamataka;T. Ando

피인용 문헌

  1. Cross-interaction constants as a measure of the transition state structure (part V). The transistion state structure for reactions of phenacyl benzenesulphonates with benzylamines in methanol vol.2, pp.6, 1987, https://doi.org/10.1002/poc.610020607
  2. Cross interaction constants as a measure of the transition state structure. 13. Steric effects of theN,N-dimethyl group on the transition state structure in aminolysis of alkyl benzenesulphonates vol.3, pp.11, 1987, https://doi.org/10.1002/poc.610031109
  3. Cross-interaction constants as a measure of the transition state structure. Part 15. Kinetic isotope effects in the SN2 reactions of 2-phenylethyl derivatives with deuterated aniline nucleophiles vol.4, pp.2, 1991, https://doi.org/10.1002/poc.610040206
  4. Bromo–nitro substitution on a tertiary α carbon—a previously uncharacterized facet of the Kornblum substitution vol.5, pp.93, 1987, https://doi.org/10.1039/c5ra14798k