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, C.A., Frasca, A.R.
Formato: JOUR
Acceso en línea: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 todo:paper_00404020_v30_n17_p2983_Mudry
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spelling todo:paper_00404020_v30_n17_p2983_Mudry2023-10-03T14:50:32Z Photochemical reactions of 2,3-diphenylindoles Mudry, C.A. Frasca, A.R. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar 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.
format JOUR
author Mudry, C.A.
Frasca, A.R.
spellingShingle Mudry, C.A.
Frasca, A.R.
Photochemical reactions of 2,3-diphenylindoles
author_facet Mudry, C.A.
Frasca, A.R.
author_sort Mudry, C.A.
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
url http://hdl.handle.net/20.500.12110/paper_00404020_v30_n17_p2983_Mudry
work_keys_str_mv AT mudryca photochemicalreactionsof23diphenylindoles
AT frascaar photochemicalreactionsof23diphenylindoles
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