First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphates

Chiral phosphotriesters are an unexplored class of ligands in metal catalysis. We wish to disclose herein the foremost application of novel chiral BINOL-derived mono- and bisphosphates in asymmetric zinc-catalyzed hydrosilylation of ketones. Corresponding alcohols were obtained in up to 92% yield an...

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Main Authors: Ngo Ndimba, Alphonsine, Roisnel, Thierry, Argouarch, Gilles, Lalli, Claudia
Format: Article
Language:English
Published: Académie des sciences 2021-03-01
Series:Comptes Rendus. Chimie
Subjects:
Online Access:https://comptes-rendus.academie-sciences.fr/chimie/articles/10.5802/crchim.67/
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author Ngo Ndimba, Alphonsine
Roisnel, Thierry
Argouarch, Gilles
Lalli, Claudia
author_facet Ngo Ndimba, Alphonsine
Roisnel, Thierry
Argouarch, Gilles
Lalli, Claudia
author_sort Ngo Ndimba, Alphonsine
collection DOAJ
description Chiral phosphotriesters are an unexplored class of ligands in metal catalysis. We wish to disclose herein the foremost application of novel chiral BINOL-derived mono- and bisphosphates in asymmetric zinc-catalyzed hydrosilylation of ketones. Corresponding alcohols were obtained in up to 92% yield and 34% ee.
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spelling doaj.art-7f047cb2c1744f8ab6eeef102052ecf52023-10-24T14:22:52ZengAcadémie des sciencesComptes Rendus. Chimie1878-15432021-03-01241778110.5802/crchim.6710.5802/crchim.67First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphatesNgo Ndimba, Alphonsine0Roisnel, Thierry1Argouarch, Gilles2Lalli, Claudia3Univ Rennes, CNRS, ISCR UMR 6226, F-35000 Rennes, FranceUniv Rennes, CNRS, ISCR UMR 6226, F-35000 Rennes, FranceUniv Rennes, CNRS, ISCR UMR 6226, F-35000 Rennes, FranceUniv Rennes, CNRS, ISCR UMR 6226, F-35000 Rennes, FranceChiral phosphotriesters are an unexplored class of ligands in metal catalysis. We wish to disclose herein the foremost application of novel chiral BINOL-derived mono- and bisphosphates in asymmetric zinc-catalyzed hydrosilylation of ketones. Corresponding alcohols were obtained in up to 92% yield and 34% ee.https://comptes-rendus.academie-sciences.fr/chimie/articles/10.5802/crchim.67/Chiral phosphotriestersBINOLAsymmetric catalysisEnantioselective hydrosilylationKetones
spellingShingle Ngo Ndimba, Alphonsine
Roisnel, Thierry
Argouarch, Gilles
Lalli, Claudia
First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphates
Comptes Rendus. Chimie
Chiral phosphotriesters
BINOL
Asymmetric catalysis
Enantioselective hydrosilylation
Ketones
title First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphates
title_full First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphates
title_fullStr First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphates
title_full_unstemmed First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphates
title_short First application of chiral phosphotriesters in asymmetric metal catalysis: enantioselective Zn-catalyzed hydrosilylation of ketones in the presence of BINOL-derived phosphates
title_sort first application of chiral phosphotriesters in asymmetric metal catalysis enantioselective zn catalyzed hydrosilylation of ketones in the presence of binol derived phosphates
topic Chiral phosphotriesters
BINOL
Asymmetric catalysis
Enantioselective hydrosilylation
Ketones
url https://comptes-rendus.academie-sciences.fr/chimie/articles/10.5802/crchim.67/
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