Search results for "SELE"

showing 10 items of 4721 documents

C-H Bond Arylation of Pyrazoles at the β-Position: General Conditions and Computational Elucidation for a High Regioselectivity

2021

International audience; Direct arylation of most five-membered ring heterocycles are generally easily accessible and strongly favored at the α-position using classical palladium-catalysis. Conversely, regioselective functionalization of such heterocycles at the concurrent β-position remains currently very challenging. Herein, we report general conditions for regioselective direct arylation at the β-position of pyrazoles, while C-H α-position is free. By using aryl bromides as the aryl source and a judicious choice of solvent, the arylation reaction of variously N-substituted pyrazoles simply proceeds via β-C-H bond functionalization. The β-regioselectivity is promoted by a ligand-free palla…

chemistry.chemical_element010402 general chemistryRing (chemistry)01 natural sciencesCatalysischemistry.chemical_compoundbeta-C−H arylationsolvent effectcatalysis010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryArylOrganic ChemistryRegioselectivityGeneral Chemistry[CHIM.CATA]Chemical Sciences/CatalysispalladiumCombinatorial chemistry0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryIntramolecular forceSolvent effectsProtic solventPalladiumheterocycle
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Phospholylmethano P-chirogenic-phosphine-borane as P-(η2-BH3)-chelating ligands of rhodium (I): Synthesis, characterization and asymmetric hydrogenat…

2021

International audience; The stereoselective synthesis of new phospholylmethano P-chirogenic-phosphine-borane was achieved by P-C bond formation of the bridge, using electrophilic or nucleophilic P*-building blocks. These P1CH2P2*.BH3 ligands behaved as chelating (κ1-P1)-(η2-BH3) entities towards the cationic rhodium(I) centre. The resulting chiral rhodium complexes were tested in asymmetric rhodium catalyzed hydrogenation of methyl 2-(acetamido)acrylate.

chemistry.chemical_elementBorane010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryRhodiumCatalysisInorganic Chemistrychemistry.chemical_compoundNucleophileMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryOrganic ChemistryAsymmetric hydrogenationCationic polymerizationStereoselective synthesis0104 chemical sciences3. Good healthP-chirogenic phosphine ligandCoordination chemistrychemistryAsymmetric hydrogenationElectrophilePhosphine
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Excited State N−H Tautomer Selectivity in the Singlet Energy Transfer of a Zinc(II)-Porphyrin-Truxene-Corrole Assembly

2017

International audience; An original corrole-containing polyad for S-1 energy transfer, in which one zinc(II)-porphyrin donor is linked to two free-base corrole acceptors by a truxene linker, is reported. This polyad exhibits a rapid zinc(II)-porphyrin*free-base corrole transfer (4.83x10(10)s(-1); 298K), even faster than the tautomerization in the excited state processes taking advantage of the good electronic communication provided by the truxene bridge. Importantly, the energy transfer process shows approximately 3-fold selectivity for one corrole N-H tautomer over the other even at low temperature (77K). This selectivity is due to the difference in the J-integral being effective in both t…

chemistry.chemical_elementDexter energy transferZinccore-modified corroles010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesmain-group elements[ CHIM ] Chemical SciencesCatalysisfree-base corroleschemistry.chemical_compoundmolecular-orbital methods[CHIM]Chemical SciencesSinglet stateCorrolecorrolesdensity-functional theoryvalence basis-setsphotophysical propertiestautomerization010405 organic chemistrytruxenesensitized solar-cellsOrganic ChemistryGeneral ChemistryTautomerPorphyrin0104 chemical scienceschemistrymesosubstituted corrolesExcited stateFRETextended basis-setsSelectivityLinker
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ChemInform Abstract: Boron Aldol Additions with Erythrulose Derivatives: Dependence of Stereoselectivity on the Type of Protecting Group.

2010

Abstract Boron aldol additions of 1- O -silylated 3,4-di- O -benzyl- and 3,4-di- O -benzoyl- l -erythrulose and achiral aldehydes using dicyclohexylboron chloride have been investigated. The dibenzyl derivative gave syn/syn stereoisomers with high stereoselectivity, whereas the dibenzoyl derivative gave syn/anti stereoisomers. It is believed that, while the dibenzoyl erythrulose gives rise to the E enolate in the presence of dicyclohexylboron chloride, as usually observed with this reagent, only the Z enolate is formed in the case of the dibenzyl derivative.

chemistry.chemical_elementErythruloseGeneral MedicineMedicinal chemistryChloridechemistry.chemical_compoundchemistryAldol reactionReagentmedicineStereoselectivityBoronProtecting groupmedicine.drugChemInform
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Electrochemical monitoring of the oxidative coupling of alkynes catalyzed by triphenylphosphine gold complexes

2012

Electrochemical monitoring of the oxidative coupling of alkynes in the homogeneous phase through catalytic cycles involving triphenylphosphine gold complexes and selectfluor as oxidant reveals that at least two gold species in +3 and +1 oxidation states are implicated. Electrochemically driven homocoupling of terminal alkynes using molecular oxygen as the oxidant can be performed using such catalysts. Keywords: Gold catalysis, Oxidative coupling of alkynes, Oxygen, Voltammetry

chemistry.chemical_elementGold catalysisElectrochemistryPhotochemistryOxygenCombinatorial chemistryCatalysislcsh:ChemistryOxygenchemistry.chemical_compoundQUIMICA ORGANICAlcsh:Industrial electrochemistrylcsh:QD1-999chemistryHomogeneousOxidative coupling of alkynesElectrochemistryVoltammetryOxidative coupling of methaneTriphenylphosphineSelectfluorVoltammetrylcsh:TP250-261Electrochemistry Communications
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Homoleptic Pnictogen-Chalcogen Coordination Complexes

2012

The synthesis and structural characterization of dicationic selenium and tellurium analogues of the carbodiphosphorane and triphosphenium families of compounds are reported. These complexes, [Ch(dppe)][OTf](2) [Ch = Se, Te; dppe = 1,2-bis(diphenylphosphino)ethane; OTf = trifluoromethanesulfonate], are formed using [Ch](2+) reagents via a ligand-exchange protocol and represent extremely rare examples of homoleptic pnictogen → chalcogen coordination complexes. The corresponding arsenic compounds were also prepared, [Ch(dpAse)][OTf](2) [Ch = Se, Te; dpAse = 1,2-bis(diphenylarsino)ethane], exhibiting the first instance of an arsenic → chalcogen dative bond. The electronic structures of these un…

chemistry.chemical_elementPhotochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundChalcogenchemistryReagentPhysical and Theoretical ChemistryHomolepticTelluriumPnictogenTrifluoromethanesulfonateta116SeleniumArsenicInorganic Chemistry
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Synthesis of novel fluorinated building blocks via halofluorination and related reactions.

2020

A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based on electrophilic activation through halonium ions of the ring olefin bonds, followed by nucleophilic fluorination with Deoxo-Fluor®. The fluorine-containing products thus obtained were subjected to elimination reactions, yielding various fluorine-containing small-molecular entities.

chemistry.chemical_elementRing (chemistry)Full Research Paperlcsh:QD241-441Elimination reactionNucleophilelcsh:Organic chemistryfluorinePolymer chemistryHalonium ionlcsh:Sciencestereocontrolorgaaniset yhdisteetOlefin fiberkemiallinen synteesiChemistryOrganic ChemistryfluorihalofluorinationChemistryfluoroselenationElectrophileFluorineSurface modificationfunctionalizationlcsh:QBeilstein journal of organic chemistry
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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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Les enfants difficiles à table : conceptualisation et évolution

2022

L'objectif du présent article est de proposer un état des lieux des études récentes permettant d'offrir un cadre conceptuel et opérationnel au concept de comportement difficile à table, tout en mettant en lumière les conséquences psychologiques pour l'enfant, ainsi que les pratiques éducatives parentales associées. L'article ambitionne aussi de déterminer dans quelle mesure un enfant difficile est un mangeur à risque de développer ultérieurement des troubles du comportement alimentaire (anorexie mentale, ARFID), et quelles seraient les pistes à privilégier, en termes de guidance parentale, pour accompagner l'enfant.

childalimentationneophobiaSociology and Political Sciencenéophobie alimentaireselectivity[SDV.NEU.PC] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Psychology and behaviorTCAARFIDEducationsélectivité alimentaire[SDV.AEN] Life Sciences [q-bio]/Food and NutritionDevelopmental and Educational PsychologyenfantfeedingdéveloppementEnfances & Psy
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CCDC 1573804: Experimental Crystal Structure Determination

2017

Related Article: Paul J. Ragogna, Cameron Graham, Clement Millet, Amy N Price, Juuso Valijus, Michael J Cowley, Heikki Tuononen|2017|Chem.-Eur.J.|24|672|doi:10.1002/chem.201704337

chloro-{1-[2-(121416323436-hexamethyl[1121:2331-terphenyl]-22-yl)-3-(246-tri-t-butylphenyl)-1234-selenadiphosphaboretan-4-yl]-2266-tetramethylpiperidine}-gold(i) acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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