1. a The substitutive nomenclature is used here for this class of compounds, but the correct IUPAC defined nomenclature is as follows: 4a, 2-methyl-furo[2,3-d]dibenzo[b,f]oxepine; 4b, ll-chloro-2-methyl-furo[2,3-d]dibenzo[b,f|oxepine; 5a, furo[2,3-d]dibenzo[b,f]oxepine-2-carbaldehyde; 5b, 1 l-chloro-furo[2,3-d]dibenzo[b,f|oxepine-2-carbalde-hyde; 6a, furo[2,3-d]dibenzo[b,f]oxepine-2-methanol; 6b, 11-chloro-furo[2,3-d]dibenzo[b,f]oxepine-2-methanol; 7, ll-chloro-furo[2,3-d]-dibenzo[b,f]oxepine-2-ylmethyl acetate;
2. Revisiting the Ullmann−Ether Reaction: A Concise and Amenable Synthesis of Novel Dibenzoxepino[4,5-d]pyrazoles by Intramolecular Etheration of 4,5-(o,o‘-Halohydroxy)arylpyrazoles
3. Nonsteroidal antiinflammatory agents. 1. 10,11-Dihydro-11-oxodibenz[b,f]oxepinacetic acids and related compounds
4. Tricyclics with analgesic and antidepressant activity. 1. [[(Alkylamino)ethyl]thio]dibenz[b,f]oxepins and 10,11-dihydro derivatives
5. Synthesis and analgesic activity of some spiro[dibenz[b,f]oxepin-10,4'-piperidine] derivatives