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Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions
Several bis(α-aminophosphonates) have been conveniently prepared in good yields using a straightforward multicomponent Kabachnik–Fields reaction between ethane 1,2-diamine or propane 1,3-diamine, diethylphosphite and aldehydes under catalyst-free conditions. The nucleophilic substitution reaction of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302223/ https://www.ncbi.nlm.nih.gov/pubmed/37375233 http://dx.doi.org/10.3390/molecules28124678 |
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author | Souii, Ichrak Sanhoury, Med Abderrahmane Vicario, Javier Jiménez-Aberásturi, Xabier Efrit, Mohamed L. M’rabet, Hedi de los Santos, Jesús M. |
author_facet | Souii, Ichrak Sanhoury, Med Abderrahmane Vicario, Javier Jiménez-Aberásturi, Xabier Efrit, Mohamed L. M’rabet, Hedi de los Santos, Jesús M. |
author_sort | Souii, Ichrak |
collection | PubMed |
description | Several bis(α-aminophosphonates) have been conveniently prepared in good yields using a straightforward multicomponent Kabachnik–Fields reaction between ethane 1,2-diamine or propane 1,3-diamine, diethylphosphite and aldehydes under catalyst-free conditions. The nucleophilic substitution reaction of bis(α-aminophosphonates) prepared and ethyl (2-bromomethyl)acrylate under mild reaction conditions afforded an original synthetic approach to a new series of bis(allylic-α-aminophosphonates). |
format | Online Article Text |
id | pubmed-10302223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103022232023-06-29 Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions Souii, Ichrak Sanhoury, Med Abderrahmane Vicario, Javier Jiménez-Aberásturi, Xabier Efrit, Mohamed L. M’rabet, Hedi de los Santos, Jesús M. Molecules Article Several bis(α-aminophosphonates) have been conveniently prepared in good yields using a straightforward multicomponent Kabachnik–Fields reaction between ethane 1,2-diamine or propane 1,3-diamine, diethylphosphite and aldehydes under catalyst-free conditions. The nucleophilic substitution reaction of bis(α-aminophosphonates) prepared and ethyl (2-bromomethyl)acrylate under mild reaction conditions afforded an original synthetic approach to a new series of bis(allylic-α-aminophosphonates). MDPI 2023-06-09 /pmc/articles/PMC10302223/ /pubmed/37375233 http://dx.doi.org/10.3390/molecules28124678 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Souii, Ichrak Sanhoury, Med Abderrahmane Vicario, Javier Jiménez-Aberásturi, Xabier Efrit, Mohamed L. M’rabet, Hedi de los Santos, Jesús M. Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions |
title | Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions |
title_full | Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions |
title_fullStr | Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions |
title_full_unstemmed | Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions |
title_short | Synthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditions |
title_sort | synthesis and characterization of a new series of bis(allylic-α-aminophosphonates) under mild reaction conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302223/ https://www.ncbi.nlm.nih.gov/pubmed/37375233 http://dx.doi.org/10.3390/molecules28124678 |
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