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: Mudry, Carlos Alberto, Frasca, Adolfo Rafael
Publicado: 1974
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
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id paper:paper_00404020_v30_n17_p2983_Mudry
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spelling paper:paper_00404020_v30_n17_p2983_Mudry2023-06-08T15:04:08Z Photochemical reactions of 2,3-diphenylindoles Mudry, Carlos Alberto Frasca, Adolfo Rafael 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. Fil:Mudry, C.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Frasca, A.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1974 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
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description 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.
author Mudry, Carlos Alberto
Frasca, Adolfo Rafael
spellingShingle Mudry, Carlos Alberto
Frasca, Adolfo Rafael
Photochemical reactions of 2,3-diphenylindoles
author_facet Mudry, Carlos Alberto
Frasca, Adolfo Rafael
author_sort Mudry, Carlos Alberto
title Photochemical reactions of 2,3-diphenylindoles
title_short Photochemical reactions of 2,3-diphenylindoles
title_full Photochemical reactions of 2,3-diphenylindoles
title_fullStr Photochemical reactions of 2,3-diphenylindoles
title_full_unstemmed Photochemical reactions of 2,3-diphenylindoles
title_sort photochemical reactions of 2,3-diphenylindoles
publishDate 1974
url 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
work_keys_str_mv AT mudrycarlosalberto photochemicalreactionsof23diphenylindoles
AT frascaadolforafael photochemicalreactionsof23diphenylindoles
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