0000000000072585

AUTHOR

Marie-joëlle Eymin

showing 15 related works from this author

Modular Hemisyntheses of Boronato- and Trifluoroborato-SubstitutedL-NHBoc Amino Acid and Peptide Derivatives

2013

Modular hemisyntheses of boronato- and trifluoroborato-substituted amino acid and peptide derivatives by using Wittig and C–H iridium-catalyzed borylation as key reactions, are described. Amino ester precursors bearing an aromatic moiety on a lateral chain were prepared by reaction of a new L-NHBoc-amino acid Wittig reagent with the corresponding aromatic aldehydes. After esterification and hydrogenation, the borylation of amino esters was achieved with yields up to 82 % by using the catalysed reaction of bis(pinacolato) diborane reagent (B2Pin2) in the presence of an iridium complex. Interestingly, this iridium-catalyzed borylation was also performed with a dipeptide in 78 % yield. Finally…

chemistry.chemical_classificationDipeptideAmino estersOrganic ChemistryPeptideBorylationCombinatorial chemistryAmino acidHydrolysischemistry.chemical_compoundchemistryReagentWittig reactionPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Phosphonium-Boronate Amino Acid Derivatives as Fluoride Pincers for 18F-Labelling

2015

The synthesis of phosphonium-boronate amino acid derivatives was achieved by quaternization of o-boronatophenylphosphine with iodo-amino acid derivatives. Preliminary radiolabelling studies demonst...

inorganic chemicalschemistry.chemical_classificationOrganic Chemistrydigestive systemBiochemistryAmino acidInorganic Chemistrychemistry.chemical_compoundchemistryLabellingOrganic chemistryheterocyclic compoundsPhosphoniumFluoridePhosphorus, Sulfur, and Silicon and the Related Elements
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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 Stereoselective Synthesis of Boron L-amino Acid Derivatives Using Wittig and Borylation Reactions

2015

The stereoselective synthesis of a new classes of boronato- or trifluoroborato aminoacids and peptides was described using Wittig and C-H iridium borylation as key reactions. A trifluoroborato-thio...

chemistry.chemical_classificationchemistryWittig reactionchemistry.chemical_elementOrganic chemistryStereoselectivityGeneral MedicineIridiumBoronBorylationAmino acidChemInform
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Efficient Stereoselective Synthesis of Boron L-Amino Acid Derivatives Using Wittig and Borylation Reactions

2015

The stereoselective synthesis of a new classes of boronato- or trifluoroborato aminoacids and peptides was described using Wittig and C-H iridium borylation as key reactions. A trifluoroborato-thio...

Inorganic Chemistrychemistry.chemical_classificationChemistryOrganic ChemistryWittig reactionchemistry.chemical_elementOrganic chemistryStereoselectivityIridiumBoronBiochemistryBorylationAmino acidPhosphorus, Sulfur, and Silicon and the Related Elements
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o-Boronato- and o-Trifluoroborato-Phosphonium Salts Supported by L-α-Amino Acid Side Chain.

2015

The synthesis of o-boronato- and o-trifluoroborato-phosphonium salts supported by the L-amino acid side chain is described. The synthesis of these new class of amino acid derivatives was achieved by stereoselective quaternization of o-(pinacolato)boronatophenylphosphine with β- or γ-iodo amino acid derivatives which are prepared from L-serine or L-aspartic acid, respectively. The quaternization of the phosphine was performed using either iodo amino ester or carboxylic acid derivatives. In addition, free carboxylic acid and amine derivatives were obtained by saponification or HCl acidolysis of o-boronato-phosphonium amino esters, respectively. The usefulness of these compounds in peptide cou…

chemistry.chemical_classificationDipeptideAmino estersMolecular StructureChemistryCarboxylic acidOrganic ChemistryAmino acidchemistry.chemical_compoundHydrolysisOrganophosphorus CompoundsAspartic acidBoratesSide chainOrganic chemistrySaltsPhosphoniumAmino AcidsThe Journal of organic chemistry
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P-Chirogenic Phosphines Supported by Calix[4]arene: New Insight into Palladium-Catalyzed Asymmetric Allylic Substitution

2013

The first P-chirogenic mono- and diphosphine ligands supported on the upper rim of a calix[4]arene moiety were synthesized using the ephedrine methodology. The lithiated calix[4]arene mono- and dianions both react with the oxazaphospholidine–borane, prepared from ephedrine, to afford regio- and stereoselectively the corresponding calix[4]arenyl aminophosphine–boranes, by cleavage of the heterocyclic ring at the P–O bond position. Subsequent reactions with HCl and then organolithium reagent and finally decomplexation with DABCO lead to the corresponding calix[4]arenyl mono- or diphosphines. Both enantiomers of the calix[4]arenyl phosphines were obtained either by using (+)- or (−)-ephedrine …

Allylic rearrangementStereochemistryOrganic Chemistrychemistry.chemical_elementDABCOBoraneOrganolithium reagentMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryDiphosphinesMoietyPhysical and Theoretical ChemistryEnantiomerPalladiumOrganometallics
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ChemInform Abstract: Modular Hemisyntheses of Boronato- and Trifluoroborato-Substituted L-NHBoc Amino Acid and Peptide Derivatives.

2014

Modular hemisyntheses of boronato- and trifluoroborato-substituted amino acid derivatives are achieved based on the reaction of Wittig reagent (I) with aldehydes followed by Ir-catalyzed boronation.

inorganic chemicalschemistry.chemical_classificationChemistryWittig reactionOrganic chemistryPeptideGeneral MedicineAmino acidChemInform
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Multinuclear Cytotoxic Metallodrugs: Physicochemical Characterization and Biological Properties of Novel Heteronuclear Gold-Titanium Complexes

2011

An unprecedented series of titanocene-gold bi- and trimetallic complexes of the general formula [[(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)(CH(2))(n)PPh(2))TiCl(2)](m)AuCl(x)](q+) (n = 0, 2, or 4; m = 1, x = 1, q = 0 or m = 2, x = 0, q = 1) have been prepared and characterized spectroscopically. The luminescence spectroscopy and photophysics of one of the compounds, [[(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)PPh(2))TiCl(2)](2)Au]PF(6), have been investigated in 2MeTHF solution and in the solid state at 77 and 298 K. Evidence for interfragment interactions based on the comparison of electronic band positions and emission lifetimes, namely, triplet energy transfer (ET) from the Au- to the Ti-containing…

Models MolecularSpectrometry Mass Electrospray IonizationLuminescenceMagnetic Resonance SpectroscopyTransfer Excited-StatesCell SurvivalStereochemistryAntineoplastic AgentsCharge-TransferUnsaturated-HydrocarbonsCrystallography X-RayElectronic-StructuresInorganic ChemistryStructure-Activity Relationshipchemistry.chemical_compoundCell Line TumorOrganometallic CompoundsHumansPhysical and Theoretical ChemistrySpectroscopyGroup 2 organometallic chemistryTitaniumArene-Ruthenium ComplexesX-rayTitanocene dichlorideNuclear magnetic resonance spectroscopyChromophoreTitanocene DichlorideCrystallographychemistryHeteronuclear moleculeAnticancer AgentsSpectrophotometry UltravioletGoldLuminescenceGold(Iii) CompoundsPhotophysical Properties
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ChemInform Abstract: O-Boronato- and o-Trifluoroborato-Phosphonium Salts Supported by L-α-Amino Acid Side Chain.

2015

The synthesis of o-boronato- and o-trifluoroborato–phosphonium salts supported by the l-amino acid side chain is described. The synthesis of these new class of amino acid derivatives was achieved by stereoselective quaternization of o-(pinacolato)boronatophenylphosphine with β- or γ-iodo amino acid derivatives which are prepared from l-serine or l-aspartic acid, respectively. The quaternization of the phosphine was performed using either iodo amino ester or carboxylic acid derivatives. In addition, free carboxylic acid and amine derivatives were obtained by saponification or HCl acidolysis of o-boronato–phosphonium amino esters, respectively. The usefulness of these compounds in peptide cou…

chemistry.chemical_classificationchemistry.chemical_compoundHydrolysisDipeptideAmino esterschemistryCarboxylic acidAspartic acidSide chainGeneral MedicinePhosphoniumMedicinal chemistryAmino acidChemInform
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CCDC 952665: Experimental Crystal Structure Determination

2013

Related Article: Naima Khiri-Meribout, Etienne Bertrand, Jérôme Bayardon, Marie-Joëlle Eymin, Yoann Rousselin, Hélène Cattey, Daniel Fortin, Pierre D. Harvey, and Sylvain Jugé|2013|Organometallics|32|2827|doi:10.1021/om400229p

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates(S)-(-)-(o-Anisyl(phenyl)(17-chloro-25262728-tetrapropoxycalix[4]arene-5-yl)phosphino)borane
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CCDC 952664: Experimental Crystal Structure Determination

2013

Related Article: Naima Khiri-Meribout, Etienne Bertrand, Jérôme Bayardon, Marie-Joëlle Eymin, Yoann Rousselin, Hélène Cattey, Daniel Fortin, Pierre D. Harvey, and Sylvain Jugé|2013|Organometallics|32|2827|doi:10.1021/om400229p

(SS)-(-)-517-bis((Ferrocenyl(phenyl)phosphinoborane))-25262728-tetrapropoxycalix[4]arene dichloromethane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 952663: Experimental Crystal Structure Determination

2013

Related Article: Naima Khiri-Meribout, Etienne Bertrand, Jérôme Bayardon, Marie-Joëlle Eymin, Yoann Rousselin, Hélène Cattey, Daniel Fortin, Pierre D. Harvey, and Sylvain Jugé|2013|Organometallics|32|2827|doi:10.1021/om400229p

Space GroupCrystallography(S)-(+)-(o-Anisyl(phenyl)(25262728-tetrapropoxycalix[4]arene)phosphino)boraneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 952662: Experimental Crystal Structure Determination

2013

Related Article: Naima Khiri-Meribout, Etienne Bertrand, Jérôme Bayardon, Marie-Joëlle Eymin, Yoann Rousselin, Hélène Cattey, Daniel Fortin, Pierre D. Harvey, and Sylvain Jugé|2013|Organometallics|32|2827|doi:10.1021/om400229p

Space GroupCrystallographyCrystal SystemCrystal Structure(S)-(-)-(Ferrocenyl(phenyl)(25262728-tetrapropoxycalix[4]arene))phosphinoboraneCell ParametersExperimental 3D Coordinates
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