The thermal [4+2] cycloadditions of 3-acetyl-, 3-carbamoyl, and 3-ethoxycarbonylcoumarins with 2,3-dimethyl-1,3-butadiene under solvent free conditions are reported, as well as the epoxidation reactions of some adducts. Discussion is focused on the structural features of the Diels-Alder adducts and their epoxides, based upon NMR, X-ray, and mass spectral data, and supported by ab initio theoretical calculations. © 2010 by the authors.
CITATION STYLE
Flores-Larios, I. Y., López-Garrido, L., Martínez-Martínez, F. J., González, J., García-Báez, E. V., Cruz, A., & Padilla-Martínez, I. I. (2010). Thermal [4 + 2] cycloadditions of 3-acetyl-, 3-carbamoyl-, and 3-ethoxycarbonyl-coumarins with 2,3-dimethyl-1,3-butadiene under solventless conditions: A structural study. Molecules, 15(3), 1513–1530. https://doi.org/10.3390/molecules15031513
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