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Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates

This review covers the main synthetic routes to and the corresponding mechanisms of phosphoramidate formation. The synthetic routes can be separated into six categories: salt elimination, oxidative cross-coupling, azide, reduction, hydrophosphinylation, and phosphoramidate-aldehyde-dienophile (PAD)....

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Detalles Bibliográficos
Autores principales: Itumoh, Emeka J., Data, Shailja, Leitao, Erin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463754/
https://www.ncbi.nlm.nih.gov/pubmed/32823507
http://dx.doi.org/10.3390/molecules25163684
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author Itumoh, Emeka J.
Data, Shailja
Leitao, Erin M.
author_facet Itumoh, Emeka J.
Data, Shailja
Leitao, Erin M.
author_sort Itumoh, Emeka J.
collection PubMed
description This review covers the main synthetic routes to and the corresponding mechanisms of phosphoramidate formation. The synthetic routes can be separated into six categories: salt elimination, oxidative cross-coupling, azide, reduction, hydrophosphinylation, and phosphoramidate-aldehyde-dienophile (PAD). Examples of some important compounds synthesized through these routes are provided. As an important class of organophosphorus compounds, the applications of phosphoramidate compounds, are also briefly introduced.
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spelling pubmed-74637542020-09-02 Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates Itumoh, Emeka J. Data, Shailja Leitao, Erin M. Molecules Review This review covers the main synthetic routes to and the corresponding mechanisms of phosphoramidate formation. The synthetic routes can be separated into six categories: salt elimination, oxidative cross-coupling, azide, reduction, hydrophosphinylation, and phosphoramidate-aldehyde-dienophile (PAD). Examples of some important compounds synthesized through these routes are provided. As an important class of organophosphorus compounds, the applications of phosphoramidate compounds, are also briefly introduced. MDPI 2020-08-13 /pmc/articles/PMC7463754/ /pubmed/32823507 http://dx.doi.org/10.3390/molecules25163684 Text en © 2020 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Itumoh, Emeka J.
Data, Shailja
Leitao, Erin M.
Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates
title Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates
title_full Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates
title_fullStr Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates
title_full_unstemmed Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates
title_short Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates
title_sort opening up the toolbox: synthesis and mechanisms of phosphoramidates
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463754/
https://www.ncbi.nlm.nih.gov/pubmed/32823507
http://dx.doi.org/10.3390/molecules25163684
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