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Recent trends in the direct oxyphosphorylation of C–C multiple bonds

Due to the wide importance of β-phosphorylated ketones as key building-blocks in the fabrication of various pharmaceutically active organophosphorus compounds, finding new and truly efficient methods for their preparation from simple, low-cost and ubiquitous feedstock materials within a single click...

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Autores principales: Bakhtiary, Alireza, Poor Heravi, Mohammad Reza, Hassanpour, Akbar, Amini, Issa, Vessally, Esmail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690964/
https://www.ncbi.nlm.nih.gov/pubmed/35423055
http://dx.doi.org/10.1039/d0ra08074h
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author Bakhtiary, Alireza
Poor Heravi, Mohammad Reza
Hassanpour, Akbar
Amini, Issa
Vessally, Esmail
author_facet Bakhtiary, Alireza
Poor Heravi, Mohammad Reza
Hassanpour, Akbar
Amini, Issa
Vessally, Esmail
author_sort Bakhtiary, Alireza
collection PubMed
description Due to the wide importance of β-phosphorylated ketones as key building-blocks in the fabrication of various pharmaceutically active organophosphorus compounds, finding new and truly efficient methods for their preparation from simple, low-cost and ubiquitous feedstock materials within a single click is an interesting subject in organic synthesis. Recently, oxyfunctionalization of carbon–carbon multiple bonds has arisen as a straightforward and versatile tool for the synthesis of complex organic molecules from the simple and easily accessible alkenes/alkynes via a single operation. In this context, oxyphosphorylation of alkenes/alkynes with P(O)–H compounds has attracted considerable attention as a unique procedure for the construction of β-phosphorylated ketones. In this review, we outline the recent advances and developments in this fast-growing research field with particular emphasis on the mechanistic aspects of reaction.
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spelling pubmed-86909642022-04-13 Recent trends in the direct oxyphosphorylation of C–C multiple bonds Bakhtiary, Alireza Poor Heravi, Mohammad Reza Hassanpour, Akbar Amini, Issa Vessally, Esmail RSC Adv Chemistry Due to the wide importance of β-phosphorylated ketones as key building-blocks in the fabrication of various pharmaceutically active organophosphorus compounds, finding new and truly efficient methods for their preparation from simple, low-cost and ubiquitous feedstock materials within a single click is an interesting subject in organic synthesis. Recently, oxyfunctionalization of carbon–carbon multiple bonds has arisen as a straightforward and versatile tool for the synthesis of complex organic molecules from the simple and easily accessible alkenes/alkynes via a single operation. In this context, oxyphosphorylation of alkenes/alkynes with P(O)–H compounds has attracted considerable attention as a unique procedure for the construction of β-phosphorylated ketones. In this review, we outline the recent advances and developments in this fast-growing research field with particular emphasis on the mechanistic aspects of reaction. The Royal Society of Chemistry 2020-12-23 /pmc/articles/PMC8690964/ /pubmed/35423055 http://dx.doi.org/10.1039/d0ra08074h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Bakhtiary, Alireza
Poor Heravi, Mohammad Reza
Hassanpour, Akbar
Amini, Issa
Vessally, Esmail
Recent trends in the direct oxyphosphorylation of C–C multiple bonds
title Recent trends in the direct oxyphosphorylation of C–C multiple bonds
title_full Recent trends in the direct oxyphosphorylation of C–C multiple bonds
title_fullStr Recent trends in the direct oxyphosphorylation of C–C multiple bonds
title_full_unstemmed Recent trends in the direct oxyphosphorylation of C–C multiple bonds
title_short Recent trends in the direct oxyphosphorylation of C–C multiple bonds
title_sort recent trends in the direct oxyphosphorylation of c–c multiple bonds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690964/
https://www.ncbi.nlm.nih.gov/pubmed/35423055
http://dx.doi.org/10.1039/d0ra08074h
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