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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...

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Detalles Bibliográficos
Autores principales: Yang, Zhiping, Gu, Xiaodong, Han, Li-Biao, Wang, Jun (Joelle)
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/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.
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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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AT hanlibiao palladiumcatalyzedasymmetrichydrophosphorylationofalkynesfacileaccesstopstereogenicphosphinates
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