Use of Kinetic Isotope Effects in Mechanism Studies. 5.1 Isotope Effects and Element Effects Associated with Hydron-Transfer Steps during Alkoxide-Promoted Dehydrohalogenations
Author:
Affiliation:
1. Contribution from the Department of Chemistry, Ithaca College, Ithaca, New York 14850, and the Leiden Institute of Chemistry, Gorlaeus Laboratories, University of Leiden, Leiden 2300RA, The Netherlands
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja970189n
Reference42 articles.
1. Use of kinetic isotope effects in mechanism studies. 4. Chlorine isotope effects associated with alkoxide-promoted dehydrochlorination reactions
2. Kinetic arguments for the existence of hydrogen bonded carbanion intermediates during dehydrohalogenation reactions of C6H5CHClCF2Y
3. Use of kinetic isotope effects in mechanism studies. Anomalous Arrhenius parameters in the study of elimination reactions
4. Proton-transfer reactions between carbon and oxygen
5. Proton-transfer reactions. I. Partitioning of carbanion intermediates generated by reactions of alkenes with alkoxide ions in alcohol
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