Effect of Lewis Acid Catalysts on Diels−Alder and Hetero-Diels−Alder Cycloadditions Sharing a Common Transition State
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, and Department of Chemistry, Boǧaziçi University, Bebek, Istanbul, 34342, Turkey
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo801076t
Reference45 articles.
1. aKraka, E.InEncyclopedia of Computational Chemistry;Schleyer, P. v. R., Ed.Wiley:New York, 1998; Vol.4, p2445.
2. bCarpenter, B. K.InReactive Intermediate Chemisty;Moss, R. A., Platz, M. S., Jones, M., Jr., Eds.Wiley-Interscience:Hoboken, NJ, 2004; pp925−960
3. Transition-State Spectroscopy of Cyclooctatetraene
4. Mechanism of Ene Reactions of Singlet Oxygen. A Two-Step No-Intermediate Mechanism
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