0000000001313198

AUTHOR

Mathieu Dutartre

showing 7 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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Luminescent P-Chirogenic Copper Clusters

2013

P-chirogenic clusters of the cubanes [Cu4I4L4] (L = chiral phosphine) were prepared from (+)- and (-)-ephedrine with L = (S)- or (R)-(R)(Ph)(i-Pr)P (with R = CH3 (seven steps) or C17H35 (10 steps)) with e.e. up to 96%. The X-ray structure of [Cu4I4((R)-(CH3)(Ph)(i-Pr)P)4] confirmed the cubane structure with average Cu···Cu and Cu···I distances of 2.954 and 2.696 Å, respectively. The cubane structure of the corresponding [Cu4I4((S)-(CH3)(Ph)(i-Pr)P)4] was established by the comparison of the X-ray powder diffraction patterns, and the opposite optical activity of the (S)- and (R)-ligand-containing clusters was confirmed by circular dichroism spectroscopy. Small-angle X-ray scattering patterns…

Circular dichroismchemistry.chemical_elementCopperInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCubaneExcited stateEmission spectrumPhysical and Theoretical ChemistryLuminescencePhosphinePowder diffractionInorganic Chemistry
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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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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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Stereoselective synthesis of o-bromo (or iodo)aryl P-chirogenic phosphines based on aryne chemistry.

2012

The efficient synthesis of chiral or achiral tertiary phosphines bearing an o-bromo (or iodo)aryl substituent is described. The key step of this synthesis is based on the reaction of a secondary phosphine borane with the 1,2-dibromo (or diiodo)arene, owing to the formation in situ of an aryne species in the presence of n-butyllithium. When P-chirogenic secondary phosphine boranes were used, the corresponding o-halogeno-arylphosphine boranes were obtained without racemization in moderate to good yields and with ee up to 99%. The stereochemistry of the reaction, with complete retention of the configuration at the P atom, has been established by X-ray structures of P-chirogenic o-halogenopheny…

[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryStereochemistryArylOrganic ChemistrySubstituentBoranesDABCOBorane010402 general chemistry01 natural sciencesMedicinal chemistryAryne0104 chemical scienceschemistry.chemical_compoundRacemizationComputingMilieux_MISCELLANEOUSPhosphineThe Journal of organic chemistry
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CCDC 1424523: Experimental Crystal Structure Determination

2015

Related Article: Antony Lapprand, Mathieu Dutartre, Naïma Khiri, Etienne Levert, Daniel Fortin, Yoann Rousselin, Armand Soldera, Sylvain Jugé and Pierre D. Harvey|2013|Inorg.Chem.|52|7958|doi:10.1021/ic400498j

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterstetrakis(mu-iodo)-tetrakis(isopropyl(methyl)phenylphosphine)-tetra-copperExperimental 3D Coordinates
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