Barrier Widths and Tunneling in the Four-Centered Syn Elimination of H-X from Ethyl-X. The Role of Transition State Asymmetry
- 1 January 1993
- journal article
- research article
- Published by Wiley in Israel Journal of Chemistry
- Vol. 33 (3), 295-305
- https://doi.org/10.1002/ijch.199300036
Abstract
No abstract availableKeywords
This publication has 64 references indexed in Scilit:
- Ab initio transition structures for hydroborations of alkenes, allenes, and alkynes by borane, diborane, methylborane, methylfluoroborane, and dimethylboraneThe Journal of Organic Chemistry, 1990
- Conformation–activity relationships and the mechanism of action of penicillinCanadian Journal of Chemistry, 1988
- The structure of n-alkanes: High precision a b i n i t i o calculation and relation to vibrational spectraThe Journal of Chemical Physics, 1986
- Organic transition states. IV. Concerted elimination of hydrogen chloride from ethyl chlorideJournal of the American Chemical Society, 1975
- Marcus rate theory and the relationship between Brønsted exponents and energy of reactionJournal of the Chemical Society, Chemical Communications, 1973
- A Simple, Self-Consistent Electrostatic Model for Quantitative Prediction of the Activation Energies of Four-Center Reactions1Journal of the American Chemical Society, 1965
- The Mechanism of Hydride Transfer. II. Details of Isotope Effects in Pyridine-Diphenylborane HydrolysisJournal of the American Chemical Society, 1962
- Large Tunnelling Corrections in Chemical Reaction Rates.1 IIJournal of the American Chemical Society, 1961
- Amine Boranes. III. Hydrolysis of Pyridine Diphenylborane and the Mechanism of Hydride Transfer ReactionsJournal of the American Chemical Society, 1958
- A Correlation of Reaction RatesJournal of the American Chemical Society, 1955