References
- J. Chem. Soc., Chem. Commun. I. Lee;S. C. Sohn
- Tetrahedron Lett. I. Lee;H. K. Kang
- J. Am. Chem. Soc. v.106 J.-E. Dubois;M.-F. Ruasse;A. Argile
- Chem. Rev. v.85 W. P. Jencks
- Correlation Analysis of Organic Reactivity J. Shorter
- J. Am. Chem. Soc. v.106 E. S. Lewis;D. D. Hu
- Acc. Chem. Res. v.17 A. Williams
- J. Am. Chem. Soc. v.101 E. S. Lewis;S. Kukes
- J. Am. Chem. Soc. v.99 J. M. Wilson;R. J. Bayer;O. J. Hupe
- J. Chem. Soc., Perkin 4 G. Petrillo;M. Novi;G. Garbarino;C. Deil 'Erba
- Can. J. Chem. v.57 B.-L. Poh
- J. Am. Chem. Soc. v.108 R. V. Hoffman;J. M. Shaukweiler
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- Cross interaction constants as a measure of the transition state structure (part III). Mechanism of reactions between 1-phenylethyl benzenesulfonates with N,N-dimethylanilines vol.2, pp.1, 1987, https://doi.org/10.1002/poc.610020105
- 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
- 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
- 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
- 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