Photochemical reactions of 2,3-diphenylindoles
The UV irradiation of 2,3-diphenylindoles produces two photochemical reactions: a dehydrocyclization with formation of dibenzocarbazoles and a photo-oxygenation which yields benzophenones. Substituents on the 2,3-diphenylindole have a great influence on the reaction course and in most of the example...
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| Autores principales: | , |
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| Publicado: |
1974
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v30_n17_p2983_Mudry http://hdl.handle.net/20.500.12110/paper_00404020_v30_n17_p2983_Mudry |
| Aporte de: |
| Sumario: | The UV irradiation of 2,3-diphenylindoles produces two photochemical reactions: a dehydrocyclization with formation of dibenzocarbazoles and a photo-oxygenation which yields benzophenones. Substituents on the 2,3-diphenylindole have a great influence on the reaction course and in most of the examples here studied only one product was formed. Some considerations about the excited states involved in these reactions are presented. © 1974. |
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