Using Incoming Nucleophile Primary Hydrogen−Deuterium Kinetic Isotope Effects To Model the SN2 Transition State
- 14 July 2000
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (30), 7342-7350
- https://doi.org/10.1021/ja000441i
Abstract
No abstract availableThis publication has 50 references indexed in Scilit:
- Kinetic isotope effect study of reductions of benzophenone with complex metal hydridesJournal of the American Chemical Society, 1986
- Occurrence of electron transfer in the reduction of organic halides by lithium aluminum hydride and aluminum hydrideThe Journal of Organic Chemistry, 1984
- A simple theory for predicting the effects of substituent changes on transition-state geometryJournal of the American Chemical Society, 1967
- Chlorine Isotope Effects in the Reactions of Benzyl and Substituted Benzyl Chlorides with Various NucleophilesJournal of the American Chemical Society, 1962
- 198. Nucleophilic reactivity. Part II. The reaction between substituted thiophenols and benzyl bromidesJournal of the Chemical Society, 1962
- Hydroboration. V. A Study of Convenient New Preparative Procedures for the Hydroboration of OlefinsJournal of the American Chemical Society, 1960
- Use of Hydrogen Isotope Effects to Identify the Attacking Nucleophile in the Enolization of Ketones Catalyzed by Acetic Acid1-3Journal of the American Chemical Society, 1958
- Amine Boranes. III. Hydrolysis of Pyridine Diphenylborane and the Mechanism of Hydride Transfer ReactionsJournal of the American Chemical Society, 1958
- The Reaction of Lewis Acids of Boron with Sodium Hydride and Borohydride1,Journal of the American Chemical Society, 1958
- Concerted Displacement Reactions. VI. m- and p-Substituent Effects as Evidence for a Unity of Mechanism in Organic Halide Reactions1Journal of the American Chemical Society, 1951