Transition State Distortion Energies Correlate with Activation Energies of 1,4-Dihydrogenations and Diels−Alder Cycloadditions of Aromatic Molecules
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, 607 Charles E. Young Drive, Los Angeles, California 90095-1569
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja809142x
Reference39 articles.
1. Uncatalyzed 1,4-hydrogenation of polycyclic aromatic hydrocarbons: A computational study
2. A primer for the Bema Hapothle. An empirical approach to the characterization of changing transition-state structures
3. Hydrogenation of Simple Aromatic Molecules: A Computational Study of the Mechanism
4. Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity
5. Theory of 1,3-Dipolar Cycloadditions: Distortion/Interaction and Frontier Molecular Orbital Models
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