Base-catalysed exchange of 2,4-di-p-anisoylbicyclo[3.2.1]octa-2,6-diene (10) proceeds faster than that of 2,4-di-p-anisoylbicyclo[3.2.1]oct-2-ene (13) indicating the significance of homoaromaticity in anions and the utility of the electron-demand tool to detect such interactions.
A. Tuncay, M. A. Carroll, L. A. Labeots and J. M. Pawlak, J. Chem. Soc., Chem. Commun., 1988, 1590 DOI: 10.1039/C39880001590
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