Abstract
The NMR spectra of the cyclohexadienyl anion and of the cyclooctadienyl anion (I) were studied. The strongly bent anion I shows at low temps. reversible line broadening. At higher temps. I electrocyclizes to the bicyclo[3.3.0]octenyl anion. In neither of these anions there is substantial 1,5 overlap (homoaromaticity). [on SciFinder (R)]
Original language | English |
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Pages (from-to) | 368-374 |
Journal | Recueil des Travaux Chimiques des Pays-Bas |
Volume | 89 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1970 |