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High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach
We report herein the synthesis of substituted 2--[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)phenyl]-1-arylethanols, ethyl 3-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)-phenyl]-2-hydroxypropanoate and 2-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)benzyl]-2-hydroxy-acenaphthylen-1(2H)-one from the reactio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264209/ https://www.ncbi.nlm.nih.gov/pubmed/21841727 http://dx.doi.org/10.3390/molecules16086883 |
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author | Juspin, Thierry Zink, Laura Crozet, Maxime D. Terme, Thierry Vanelle, Patrice |
author_facet | Juspin, Thierry Zink, Laura Crozet, Maxime D. Terme, Thierry Vanelle, Patrice |
author_sort | Juspin, Thierry |
collection | PubMed |
description | We report herein the synthesis of substituted 2--[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)phenyl]-1-arylethanols, ethyl 3-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)-phenyl]-2-hydroxypropanoate and 2-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)benzyl]-2-hydroxy-acenaphthylen-1(2H)-one from the reactions of 4-[4-(chloromethyl)phenyl]-1,2-dimethyl-5-nitro-1H-imidazole with various aromatic carbonyl and α-carbonyl ester derivatives using tetrakis(dimethylamino)ethylene (TDAE) methodology. |
format | Online Article Text |
id | pubmed-6264209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62642092018-12-10 High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach Juspin, Thierry Zink, Laura Crozet, Maxime D. Terme, Thierry Vanelle, Patrice Molecules Communication We report herein the synthesis of substituted 2--[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)phenyl]-1-arylethanols, ethyl 3-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)-phenyl]-2-hydroxypropanoate and 2-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)benzyl]-2-hydroxy-acenaphthylen-1(2H)-one from the reactions of 4-[4-(chloromethyl)phenyl]-1,2-dimethyl-5-nitro-1H-imidazole with various aromatic carbonyl and α-carbonyl ester derivatives using tetrakis(dimethylamino)ethylene (TDAE) methodology. MDPI 2011-08-12 /pmc/articles/PMC6264209/ /pubmed/21841727 http://dx.doi.org/10.3390/molecules16086883 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. 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 | Communication Juspin, Thierry Zink, Laura Crozet, Maxime D. Terme, Thierry Vanelle, Patrice High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach |
title | High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach |
title_full | High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach |
title_fullStr | High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach |
title_full_unstemmed | High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach |
title_short | High Functionalization of 5-Nitro-1H-imidazole Derivatives: The TDAE Approach |
title_sort | high functionalization of 5-nitro-1h-imidazole derivatives: the tdae approach |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264209/ https://www.ncbi.nlm.nih.gov/pubmed/21841727 http://dx.doi.org/10.3390/molecules16086883 |
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