Recent work on the synthesis of 3,6‐dibenzoylcarbazole

By heating carbazole (1) with aluminum trichloride and benzoyl chloride four benzoylcarbazole derivatives were obtained: N‐benzoylcarbazole (2), 1‐benzoylcarbazole (3), 3‐benzoylcarbazole (4) and 3,6‐dibenzoylcarbazole (5). The complete characterization of benzoylcarbazole derivatives 2–5 was perfor...

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Autor principal: Bonesi, Sergio Mauricio
Publicado: 1991
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v28_n4_p1035_Bonesi
http://hdl.handle.net/20.500.12110/paper_0022152X_v28_n4_p1035_Bonesi
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id paper:paper_0022152X_v28_n4_p1035_Bonesi
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spelling paper:paper_0022152X_v28_n4_p1035_Bonesi2023-06-08T14:46:43Z Recent work on the synthesis of 3,6‐dibenzoylcarbazole Bonesi, Sergio Mauricio By heating carbazole (1) with aluminum trichloride and benzoyl chloride four benzoylcarbazole derivatives were obtained: N‐benzoylcarbazole (2), 1‐benzoylcarbazole (3), 3‐benzoylcarbazole (4) and 3,6‐dibenzoylcarbazole (5). The complete characterization of benzoylcarbazole derivatives 2–5 was performed by physical and spectroscopical methods (mp, tlc Rf, glc Tr, uv, ir, 1H nmr, 13C nmr and ms). Copyright © 1991 Journal of Heterocyclic Chemistry Fil:Bonesi, S.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1991 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v28_n4_p1035_Bonesi http://hdl.handle.net/20.500.12110/paper_0022152X_v28_n4_p1035_Bonesi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description By heating carbazole (1) with aluminum trichloride and benzoyl chloride four benzoylcarbazole derivatives were obtained: N‐benzoylcarbazole (2), 1‐benzoylcarbazole (3), 3‐benzoylcarbazole (4) and 3,6‐dibenzoylcarbazole (5). The complete characterization of benzoylcarbazole derivatives 2–5 was performed by physical and spectroscopical methods (mp, tlc Rf, glc Tr, uv, ir, 1H nmr, 13C nmr and ms). Copyright © 1991 Journal of Heterocyclic Chemistry
author Bonesi, Sergio Mauricio
spellingShingle Bonesi, Sergio Mauricio
Recent work on the synthesis of 3,6‐dibenzoylcarbazole
author_facet Bonesi, Sergio Mauricio
author_sort Bonesi, Sergio Mauricio
title Recent work on the synthesis of 3,6‐dibenzoylcarbazole
title_short Recent work on the synthesis of 3,6‐dibenzoylcarbazole
title_full Recent work on the synthesis of 3,6‐dibenzoylcarbazole
title_fullStr Recent work on the synthesis of 3,6‐dibenzoylcarbazole
title_full_unstemmed Recent work on the synthesis of 3,6‐dibenzoylcarbazole
title_sort recent work on the synthesis of 3,6‐dibenzoylcarbazole
publishDate 1991
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v28_n4_p1035_Bonesi
http://hdl.handle.net/20.500.12110/paper_0022152X_v28_n4_p1035_Bonesi
work_keys_str_mv AT bonesisergiomauricio recentworkonthesynthesisof36dibenzoylcarbazole
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