Antiaromaticity Gain Activates Tropone and Nonbenzenoid Aromatics as Normal-Electron-Demand Diels–Alder Dienes
Author:
Affiliation:
1. Department of Chemistry, University of Houston, Houston, Texas 77204, United States
2. Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306, United States
Funder
Division of Chemistry
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c02343
Reference43 articles.
1. Diels-Alder Reaction of Tropolones with Maleic Anhydride
2. Novel Two-Step Synthesis of Homobarrelenones, Bicyclo[3.2.2]nona-3,6,8-trien-2-ones, from Tropones and 2,3-Bis(methoxycarbonyl)-7-oxabicyclo[2.2.1]heptadiene by High-Pressure Cycloaddition-Thermal Cycloreversion Procedure
3. Novel Preparation of 1- and 3-Substituted Bicyclo[3.2.2]nona-3,6,8-trien-2-ones from Tropones and 2,3-Bis(methoxycarbonyl)-7-oxabicyclo[2.2.1]heptadiene by High-Pressure Cydoaddition-Thermal Cycloreversion Procedure
4. Use of cycloaddition reactions and photochemical transformations in the preparation of norcarane derivatives
5. Lewis Acid Catalyzed Inverse-Electron-Demand Diels−Alder Reaction of Tropones
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