Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles

A simple and efficient synthesis of novel 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles, utilizing sodium ethoxide as a catalyst via a Friedländer condensation reaction between 3-acetyl-9-ethyl-9H-carbazole or 3,6-diacetyl-9-ethyl-9H-carbazole and β-aminoaldehydes or β-aminoketones is...

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Detalles Bibliográficos
Autores principales: Li, Yang, Gao, Wentao
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2010
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2981831/
https://www.ncbi.nlm.nih.gov/pubmed/21085511
http://dx.doi.org/10.3762/bjoc.6.108
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author Li, Yang
Gao, Wentao
author_facet Li, Yang
Gao, Wentao
author_sort Li, Yang
collection PubMed
description A simple and efficient synthesis of novel 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles, utilizing sodium ethoxide as a catalyst via a Friedländer condensation reaction between 3-acetyl-9-ethyl-9H-carbazole or 3,6-diacetyl-9-ethyl-9H-carbazole and β-aminoaldehydes or β-aminoketones is described. All of the title compounds were obtained in good yields of 52–72% and their structures were confirmed by IR, (1)H NMR, MS, and elemental analysis.
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spelling pubmed-29818312010-11-17 Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles Li, Yang Gao, Wentao Beilstein J Org Chem Full Research Paper A simple and efficient synthesis of novel 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles, utilizing sodium ethoxide as a catalyst via a Friedländer condensation reaction between 3-acetyl-9-ethyl-9H-carbazole or 3,6-diacetyl-9-ethyl-9H-carbazole and β-aminoaldehydes or β-aminoketones is described. All of the title compounds were obtained in good yields of 52–72% and their structures were confirmed by IR, (1)H NMR, MS, and elemental analysis. Beilstein-Institut 2010-10-08 /pmc/articles/PMC2981831/ /pubmed/21085511 http://dx.doi.org/10.3762/bjoc.6.108 Text en Copyright © 2010, Li and Gao https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Li, Yang
Gao, Wentao
Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles
title Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles
title_full Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles
title_fullStr Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles
title_full_unstemmed Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles
title_short Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles
title_sort synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9h-carbazoles
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2981831/
https://www.ncbi.nlm.nih.gov/pubmed/21085511
http://dx.doi.org/10.3762/bjoc.6.108
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AT gaowentao synthesisof3quinolin2yland36bisquinolin2yl9hcarbazoles

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