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Electrophilic substitution of dibenz[b,f]oxepin |
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| Authors: | P. M. G. Bavin K. D. Bartle D. W. Jones |
| Abstract: | Dibenz[b,f]oxepin undergoes nitration and acid-catalyzed deuteration at the 10-position and adds bromine across the 10,11 bond. These reactions contradict predictions made by the SCFMO method. Chemical reactions and NMR spectroscopy suggest that dibenz[b,f]oxepin is only weakly aromatic. |
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