Lewis Acid Catalysis Alters the Shapes and Products of Bis-Pericyclic Diels−Alder Transition States
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, and Department of Chemistry, Boǧaziçi University, Bebek, Istanbul 34342, Turkey
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja070686w
Reference22 articles.
1. An Unexpected Bispericyclic Transition Structure Leading to 4+2 and 2+4 Cycloadducts in the Endo Dimerization of Cyclopentadiene
2. Merging and bifurcation of 4+2 and 2+4 cycloaddition modes in the archetypal dimerization of butadiene. A case of competing bispericyclic, pericyclic and diradical paths
3. A Bispericyclic Transition Structure Allows for Efficient Relief of Antiaromaticity Enhancing Reactivity and Endo Stereoselectivity in the Dimerization of the Fleeting Cyclopentadienone
4. Density Functional Theory Study on Dimerizations of Phospholes
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