Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Cross Interaction Constants in Elimination Reactions

  • Published : 1987.10.20
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Abstract

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References

  1. J. Chem. Soc., Chem. Commun. I. Lee;S. C. Sohn
  2. Tetrahedron Lett. v.22 I. Lee;H. K. Kang
  3. Tetrahedron Lett. v.8 I. Lee
  4. J. Org. Chem. v.33 J.F. Kirsch;W. Clewell;A. Simon
  5. Mechanism and Theory in Organic Chemistry T. H. Lowry;K. S. Richardson
  6. Mechanism and Theory in Organic Chemistry T. H. Lowry;K. S. Richardson
  7. J. Org. Chem. v.51 A. S. Shawali;A. Harhash;M. M. Sidky;H. M. Hassaneen;S. S. Elkaabi
  8. J. Am. Chem. Soc. v.94 F. M. Menger;J. H. Smith

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  2. 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
  3. Cross-interaction constants as a measure of the transition state structure. Part 8. Mechanism of the reaction of 2-phenylethyl benzenesulphonates with benzylamine in acetonitrile vol.3, pp.8, 1987, https://doi.org/10.1002/poc.610030808
  4. Cross-interaction constants as a measure of the transition state structure. Part 9. The degree of bond formation in theSN2 transition state involving anionic nucleophiles vol.3, pp.8, 1990, https://doi.org/10.1002/poc.610030809
  5. 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