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Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates
Despite the importance of P-chiral organophosphorus compounds in asymmetric catalysis, transition metal-catalyzed methods for accessing P-chiral phosphine derivatives are still limited. Herein, a catalytic enantioselective method for the synthesis of P-stereogenic alkenylphosphinates is developed th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159285/ https://www.ncbi.nlm.nih.gov/pubmed/34123027 http://dx.doi.org/10.1039/d0sc01049a |
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author | Yang, Zhiping Gu, Xiaodong Han, Li-Biao Wang, Jun (Joelle) |
author_facet | Yang, Zhiping Gu, Xiaodong Han, Li-Biao Wang, Jun (Joelle) |
author_sort | Yang, Zhiping |
collection | PubMed |
description | Despite the importance of P-chiral organophosphorus compounds in asymmetric catalysis, transition metal-catalyzed methods for accessing P-chiral phosphine derivatives are still limited. Herein, a catalytic enantioselective method for the synthesis of P-stereogenic alkenylphosphinates is developed through asymmetric hydrophosphorylation of alkynes. This process is demonstrated for a wide range of racemic phosphinates and leads to diverse P-stereogenic alkenylphosphinates directly. |
format | Online Article Text |
id | pubmed-8159285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81592852021-06-11 Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates Yang, Zhiping Gu, Xiaodong Han, Li-Biao Wang, Jun (Joelle) Chem Sci Chemistry Despite the importance of P-chiral organophosphorus compounds in asymmetric catalysis, transition metal-catalyzed methods for accessing P-chiral phosphine derivatives are still limited. Herein, a catalytic enantioselective method for the synthesis of P-stereogenic alkenylphosphinates is developed through asymmetric hydrophosphorylation of alkynes. This process is demonstrated for a wide range of racemic phosphinates and leads to diverse P-stereogenic alkenylphosphinates directly. The Royal Society of Chemistry 2020-06-29 /pmc/articles/PMC8159285/ /pubmed/34123027 http://dx.doi.org/10.1039/d0sc01049a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yang, Zhiping Gu, Xiaodong Han, Li-Biao Wang, Jun (Joelle) Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates |
title | Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates |
title_full | Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates |
title_fullStr | Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates |
title_full_unstemmed | Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates |
title_short | Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates |
title_sort | palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to p-stereogenic phosphinates |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159285/ https://www.ncbi.nlm.nih.gov/pubmed/34123027 http://dx.doi.org/10.1039/d0sc01049a |
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