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Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives
Symmetrical and unsymmetrical 3-halo- or 3-methoxy- substituted 2-dibenzoylamino-1,4-naphthoquinone analogs were synthesized with an average yield of 45% via sodium hydride promoted bis-acylation of 2-amino-3-chloro-1,4-naphthoquinone, 2-amino-3-bromo-1,4-naphthoquinone and 2-amino-3-methoxy-1,4-nap...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654863/ https://www.ncbi.nlm.nih.gov/pubmed/23381023 http://dx.doi.org/10.3390/molecules18021973 |
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author | Brandy, Yakini Brandy, Nailah Akinboye, Emmanuel Lewis, Malik Mouamba, Claudia Mack, Seshat Butcher, Ray J. Anderson, Alan J. Bakare, Oladapo |
author_facet | Brandy, Yakini Brandy, Nailah Akinboye, Emmanuel Lewis, Malik Mouamba, Claudia Mack, Seshat Butcher, Ray J. Anderson, Alan J. Bakare, Oladapo |
author_sort | Brandy, Yakini |
collection | PubMed |
description | Symmetrical and unsymmetrical 3-halo- or 3-methoxy- substituted 2-dibenzoylamino-1,4-naphthoquinone analogs were synthesized with an average yield of 45% via sodium hydride promoted bis-acylation of 2-amino-3-chloro-1,4-naphthoquinone, 2-amino-3-bromo-1,4-naphthoquinone and 2-amino-3-methoxy-1,4-naphthoquinone. |
format | Online Article Text |
id | pubmed-3654863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-36548632013-05-15 Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives Brandy, Yakini Brandy, Nailah Akinboye, Emmanuel Lewis, Malik Mouamba, Claudia Mack, Seshat Butcher, Ray J. Anderson, Alan J. Bakare, Oladapo Molecules Article Symmetrical and unsymmetrical 3-halo- or 3-methoxy- substituted 2-dibenzoylamino-1,4-naphthoquinone analogs were synthesized with an average yield of 45% via sodium hydride promoted bis-acylation of 2-amino-3-chloro-1,4-naphthoquinone, 2-amino-3-bromo-1,4-naphthoquinone and 2-amino-3-methoxy-1,4-naphthoquinone. MDPI 2013-02-04 /pmc/articles/PMC3654863/ /pubmed/23381023 http://dx.doi.org/10.3390/molecules18021973 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Brandy, Yakini Brandy, Nailah Akinboye, Emmanuel Lewis, Malik Mouamba, Claudia Mack, Seshat Butcher, Ray J. Anderson, Alan J. Bakare, Oladapo Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives |
title | Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives |
title_full | Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives |
title_fullStr | Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives |
title_full_unstemmed | Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives |
title_short | Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives |
title_sort | synthesis and characterization of novel unsymmetrical and symmetrical 3-halo- or 3-methoxy-substituted 2-dibenzoylamino-1,4-naphthoquinone derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654863/ https://www.ncbi.nlm.nih.gov/pubmed/23381023 http://dx.doi.org/10.3390/molecules18021973 |
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