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A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes
1,2-Bis(dialkylphosphino)ethanes are readily prepared from the parent phosphine oxides, via a novel sodium aluminium hydride/sodium hydride reduction protocol of intermediate chlorophosphonium chlorides. This approach is amenable to multi-gram syntheses, utilises readily available and inexpensive re...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498470/ https://www.ncbi.nlm.nih.gov/pubmed/26190960 http://dx.doi.org/10.1002/adsc.201300787 |
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author | Doyle, Laurence R Heath, Alex Low, Choon Heng Ashley, Andrew E |
author_facet | Doyle, Laurence R Heath, Alex Low, Choon Heng Ashley, Andrew E |
author_sort | Doyle, Laurence R |
collection | PubMed |
description | 1,2-Bis(dialkylphosphino)ethanes are readily prepared from the parent phosphine oxides, via a novel sodium aluminium hydride/sodium hydride reduction protocol of intermediate chlorophosphonium chlorides. This approach is amenable to multi-gram syntheses, utilises readily available and inexpensive reagents, and benefits from a facile non-aqueous work-up in the final reductive step. |
format | Online Article Text |
id | pubmed-4498470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-44984702015-07-15 A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes Doyle, Laurence R Heath, Alex Low, Choon Heng Ashley, Andrew E Adv Synth Catal Updates 1,2-Bis(dialkylphosphino)ethanes are readily prepared from the parent phosphine oxides, via a novel sodium aluminium hydride/sodium hydride reduction protocol of intermediate chlorophosphonium chlorides. This approach is amenable to multi-gram syntheses, utilises readily available and inexpensive reagents, and benefits from a facile non-aqueous work-up in the final reductive step. WILEY-VCH Verlag 2014-02-10 2014-02-02 /pmc/articles/PMC4498470/ /pubmed/26190960 http://dx.doi.org/10.1002/adsc.201300787 Text en © 2014 The authors. Published by Wiley-VCH Verlag GmbH &Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. https://creativecommons.org/licenses/by-nc-nd/4.0/ © 2014 The authors. Published by Wiley-VCH Verlag GmbH &Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Updates Doyle, Laurence R Heath, Alex Low, Choon Heng Ashley, Andrew E A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes |
title | A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes |
title_full | A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes |
title_fullStr | A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes |
title_full_unstemmed | A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes |
title_short | A Convenient Synthetic Protocol to 1,2-Bis(dialkylphosphino)ethanes |
title_sort | convenient synthetic protocol to 1,2-bis(dialkylphosphino)ethanes |
topic | Updates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498470/ https://www.ncbi.nlm.nih.gov/pubmed/26190960 http://dx.doi.org/10.1002/adsc.201300787 |
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