0000000000177819

AUTHOR

Jerome Bayardon

showing 8 related works from this author

ChemInform Abstract: P-Chirogenic Secondary Phosphine Oxides: New Stereoselective Synthesis and Applications

2015

chemistry.chemical_compoundchemistryOrganic chemistryStereoselectivityGeneral MedicinePhosphineChemInform
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P-Chirogenic Secondary Phosphine Oxides: New Stereoselective Synthesis and Applications

2015

Inorganic Chemistrychemistry.chemical_compoundchemistryOrganic ChemistryOrganic chemistryStereoselectivityBiochemistryPhosphinePhosphorus, Sulfur, and Silicon and the Related Elements
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ChemInform Abstract: Efficient Synthesis of Quaternary and P-Stereogenic Phosphonium Triflates.

2010

An efficient and general method for the preparation of achiral and chiral phosphonium salts is reported. This synthesis is based on the quaternization of phosphines and their derivatives with arynes generated in situ from 2-(trimethylsilyl)aryl triflates. This methodology is successfully applied to the synthesis of new valuable P-stereogenic phosphonium triflates.

chemistry.chemical_compoundGeneral methodchemistryTrimethylsilylArylOrganic chemistryGeneral MedicinePhosphoniumAryneStereocenterChemInform
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ChemInform Abstract: Applications and Stereoselective Syntheses of P-Chirogenic Phosphorus Compounds

2016

Phosphorus compounds bearing chirality on the P-center are usually qualified as P-chirogenic or P-stereogenic. This chemical class concerns natural products, agrochemistry, molecular materials, biology and pharmacy, although it is certainly in coordination chemistry and in asymmetric catalysis using chiral transition metal complexes that P-chirogenic phosphorus compounds are the most used. The chiral phosphine ligands and their uses in asymmetric metal-catalyzed reactions have been widely reviewed in literature. However, an overview covering the applications as well as the stereoselective syntheses of all classes of phosphorus compounds has not yet been provided. This review reports the bes…

chemistry.chemical_classificationchemistry.chemical_compoundchemistryPhosphorusEnantioselective synthesischemistry.chemical_elementOrganic chemistryStereoselectivityGeneral MedicineMolecular materialsChirality (chemistry)PhosphineCoordination complexChemInform
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ChemInform Abstract: o-(Hydroxyalkyl)phenyl P-Chirogenic Phosphines as Functional Chiral Lewis Bases.

2013

The stereoselective synthesis of P-chirogenic phosphines bearing an o-hydroxyalkyl chain is described.

Chain (algebraic topology)ChemistryStereochemistryStereoselectivityGeneral MedicineLewis acids and basesChemInform
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Efficient synthesis of quaternary and P-stereogenic phosphonium triflates

2010

An efficient and general method for the preparation of achiral and chiral phosphonium salts is reported. This synthesis is based on the quaternization of phosphines and their derivatives with arynes generated in situ from 2-(trimethylsilyl)aryl triflates. This methodology is successfully applied to the synthesis of new valuable P-stereogenic phosphonium triflates.

General methodMolecular StructureTrimethylsilyl[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryArylOrganic ChemistryStereoisomerism010402 general chemistry01 natural sciencesBiochemistryAryne0104 chemical sciencesStereocenterchemistry.chemical_compoundOrganophosphorus Compoundschemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistryPhosphoniumPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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o-(Hydroxyalkyl)phenyl P-Chirogenic Phosphines as Functional Chiral Lewis Bases

2013

The stereoselective synthesis of P-chirogenic phosphines bearing an o-hydroxyalkyl chelating arm is described. The synthesis is based either on the hydroxyalkylation of P-chirogenic o-bromophenylphosphines (borane) or on their carbonatation and then reduction. The hydroxyalkylation with benzaldehyde or pivalaldehyde affords a mixture of epimers which are isolated by chromatography and characterized by their X-ray structures. Preliminary assays of free P-chirogenic o-(hydroxyalkyl)phenyl phosphines, as new functional Lewis bases in catalyzed asymmetric aza-MBH reaction, lead to β-aminoester derivatives with ee values up to 74%.

Benzaldehydechemistry.chemical_compoundStereochemistryChemistryOrganic ChemistryEpimerStereoselectivityChelationLewis acids and basesPhysical and Theoretical ChemistryBoraneBiochemistryCatalysisOrganic Letters
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Applications and stereoselective syntheses of P-chirogenic phosphorus compounds.

2016

International audience; Phosphorus compounds bearing chirality on the P-center are usually qualified as P-chirogenic or P-stereogenic. This chemical class concerns natural products, agrochemistry, molecular materials, biology and pharmacy, although it is certainly in coordination chemistry and in asymmetric catalysis using chiral transition metal complexes that P-chirogenic phosphorus compounds are the most used. The chiral phosphine ligands and their uses in asymmetric metal-catalyzed reactions have been widely reviewed in literature. However, an overview covering the applications as well as the stereoselective syntheses of all classes of phosphorus compounds has not yet been provided. Thi…

chemistry.chemical_elementring-closing metathesis010402 general chemistryenantioselective transfer hydrogenation[ CHIM ] Chemical Sciences01 natural sciencesCoordination complexcatalyzed asymmetric hydrogenationchemistry.chemical_compoundactive phosphine oxides[CHIM]Chemical Scienceschiral diphosphine ligandsOrganic chemistryMolecular materialstransition-metal catalysischemistry.chemical_classificationacyl-transfer catalysts010405 organic chemistryPhosphorusEnantioselective synthesisc migration rearrangementGeneral Chemistry0104 chemical scienceschemistrytert-butylphenylphosphine oxideStereoselectivityray crystal-structureChirality (chemistry)PhosphineChemical Society reviews
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