Diels−Alder Reactions of Cyclopentadiene and 9,10-Dimethylanthracene with Cyanoalkenes: The Performance of Density Functional Theory and Hartree−Fock Calculations for the Prediction of Substituent Effects
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp052055z
Reference48 articles.
1. Eine Studie der D IELS ‐A LDER ‐Reaktion, I. Die Reaktivität von Dienophilen gegenüber Cyclopentadien und 9.10‐Dimethyl‐anthracen
2. Ionization potentials, electron affinities, and reactivities of cyanoalkenes and related electron-deficient alkenes. A frontier molecular orbital treatment of cyanoalkene reactivities in cycloaddition, electrophilic, nucleophilic, and radical reactions
3. Substituent effects and transition structures for Diels-Alder reactions of butadiene and cyclopentadiene with cyanoalkenes
4. Solvent effects on endo/exo selective in (4 + 2) cycloadditions of cyanoethylenes.
5. Ab initio study of Diels-Alder reactions of cyclopentadiene with ethylene, isoprene, cyclopentadiene, acrylonitrile, and methyl vinyl ketone
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