Search results for "Selectivity"

showing 10 items of 1148 documents

Phase-selective low molecular weight organogelators derived from allylated D-mannose

2022

In the last decades, synthesis and design of low molecular weight organogelators has gained increasing attention due to their versatile use in, for example, cosmetics, biomedicine and oil spill remediation. In this work, three potential gelators have been prepared from allylated d-mannose. Both the gelators and the corresponding gels formed were thoroughly characterized by crystallography, FTIR spectroscopy, SEM, rheometry and NMR spectroscopy, in solution and in solid state. The results showed that two of the compounds phase-selectively form gels with hydrocarbon solvents. The most promising gelator compound is alkene terminated, with the unsaturated end functionality not critical for gel …

monosakkariditgeelitD-mannoosiLMWOGphase selectivityOrganic ChemistryinfrapunaspektroskopiaGeneral MedicineAlkenesgelskidetiedeBiochemistryAnalytical ChemistryMolecular WeightPetroleum PollutionhyötykäyttöNMR-spektroskopiahiilihydraatitGelsMannoseD-mannosesolid state NMR spectroscop
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A Catalyst Designed for the Enantioselective Construction of Methyl- and Alkyl-Substituted Tertiary Stereocenters

2015

Tertiary methyl-substituted stereocenters are present in numerous biologically active natural products. Reported herein is a catalytic enantioselective method for accessing these chiral building blocks using the Mukaiyama-Michael reaction between silyl ketene thioacetals and acrolein. To enable remote enantioface control on the nucleophile, a new iminium catalyst, optimized by three-parameter tuning and by identifying substituent effects on enantioselectivity, was designed. The catalytic process allows rapid access to chiral thioesters, amides, aldehydes, and ketones bearing an α-methyl stereocenter with excellent enantioselectivities, and allowed rapid access to the C4-C13 segment of (-)-b…

natural productsSubstituentKetene010402 general chemistry01 natural sciencesCatalysisStereocenterchemistry.chemical_compoundNucleophileOrganic chemistryorganocatalysista116Alkylchemistry.chemical_classification010405 organic chemistryChemistryEnantioselective synthesisIminiumasymmetric catalysisGeneral MedicineGeneral Chemistrydiastereoselectivity0104 chemical sciences3. Good healthOrganocatalysisdensity functional calculationsAngewandte Chemie International Edition
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Reactivity of asymmetric benzo-condensed diazines with nitrilimine dipoles in the 1,3-dipolar cycloaddition reactions

2009

The reactivity of asymmetric benzo-condensed diazines in the 1,3-dipolar cycloaddition reactions with nitrilimines was investigated. The results demonstrated that, at variance with the symmetric quinoxaline, a certain grade of diastereoselectivity emerged. Moreover in the case of the 5-methylquinoxaline and quinazoline a mono-cycloadduct was obtained.

nitrilimine dipoleChemistryNitrilimine13-dipolar cycloaddition reactionOrganic ChemistrydiazineSettore CHIM/06 - Chimica OrganicadiastereoselectivityPhotochemistrySettore CHIM/08 - Chimica FarmaceuticaBiochemistryCycloadditionchemistry.chemical_compoundDipoleQuinoxalineComputational chemistryDrug Discovery13-Dipolar cycloadditionQuinazolineReactivity (chemistry)Tetrahedron Letters
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Plaisir et alimentation chez la personne âgée

2018

National audience

odorfoodselectivityperceptionelderlyseniorolder adultmemorytaste[SDV.AEN] Life Sciences [q-bio]/Food and Nutritionpreferencediet[SDV.AEN]Life Sciences [q-bio]/Food and NutritionComputingMilieux_MISCELLANEOUS
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Asymmetric Organocatalytic Synthesis of 4-Aminoisochromanones via a Direct One-Pot Intramolecular Mannich Reaction

2016

Synthesis 48(24), 4451 - 4458(2016). doi:10.1055/s-0035-1562522

one-pot reaction010405 organic chemistryChemistryOrganic Chemistryasymmetric synthesisEnantioselective synthesis010402 general chemistry54001 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesCatalysisIntramolecular forceOne pot reactionOrganocatalysisddc:540isochromanonesMannich reactionOrganic chemistryAmine gas treatingStereoselectivityorganocatalysisMannich reactionorganocatalysis; one-pot reaction; asymmetric synthesis; isochromanones; Mannich reaction
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New simple hydrophobic proline derivatives as highly active and stereoselective catalysts for the direct asymmetric aldol reaction in aqueous medium

2008

New 4-substituted acyloxyproline derivatives with different hydrophobic properties of the acyl group were easily synthesized and used as catalysts in the direct asymmetric aldol reaction between cyclic ketones (cyclohexanone and cyclopentanone) and several substituted benzaldehydes. Reactions were carried out using water, this being the best reaction medium examined. Screening of these catalysts showed that compounds bearing the most hydrophobic acyl chains [4-phenylbutanoate and 4-(pyren-1-yl)butanoate] provided better results. The latter catalysts were successfully used in only 2 mol% at room temperature without additives to give aldol products in excellent stereoselectivities. These resu…

or-ganic catalysiorganic chemicalsOrganic ChemistryketoneSubstituentCyclohexanoneSettore CHIM/06 - Chimica OrganicaCyclopentanoneCatalysisaldehydeCatalysischemistry.chemical_compoundchemistryAldol reactionMoietyOrganic chemistryaldol reactionStereoselectivityprolineAcyl group
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Fluorine-containing functionalized cyclopentene scaffolds through ring contraction and deoxofluorination of various substituted cyclohexenes

2018

The fluorination of some highly‐functionalized cyclopentene derivatives, obtained from various substituted cyclohexenes through a ring‐opening/ring‐contraction procedure, has been investigated. The transformations were found to be highly substrate dependent, and led to the formation of various functionalized alicyclic compounds or heterocycles containing allyl difluoride or vinyl fluoride moieties. peerReviewed

organic chemicalsaldol reactionaminohapotstereoselectivityring contractionorgaaniset yhdisteetfluoriditfluori
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Oxidation of aromatic alcohols in irradiated aqueous suspensions of commercial and home-prepared rutile TiO(2): a selectivity study.

2008

WOS: 000256241700021

oxidationPhotochemistryUltraviolet RaysAlcoholAnisolesAldehydeAlcohols Oxidation Photocatalysis Rutile SelectivityCatalysisCatalysisalcoholschemistry.chemical_compoundX-Ray DiffractionOrganic chemistryReactivity (chemistry)chemistry.chemical_classificationTitaniumSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionalcohols;oxidation;photocatalysis;rutile;selectivityMolecular StructureOrganic ChemistryselectivityWaterGeneral ChemistrychemistryBenzyl alcoholPhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelectivityrutilephotocatalysisOxidation-ReductionBenzyl AlcoholChemistry (Weinheim an der Bergstrasse, Germany)
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Jak historia odkłada się w pamięci, jak pamięć odkłada się w języku

2019

Tematem artykułu jest zakreślenie ram pola badawczego tworzonego przez trzy tytułowe pojęcia: historia, pamięć, język. Ponieważ każde z nich jest wieloznaczne, a na dodatek w różnych sytuacjach odnoszone są do różnych porządków ontologicznych (do rzeczywistości pozajęzykowej i do rzeczywistości tekstowej, narracyjnej), autor stara się doprecyzować znaczenia odnośnych wyrazów i pokazać złożone relacje, jakie występują zarówno między poszczególnymi znaczeniami każdego z wyrazów oddzielnie (a więc pomiędzy „historią1” i „historią2” z jednej strony oraz między „pamięcią1” i „pamięcią2” – z drugiej), jak też, w układzie „horyzontalnym”, między „historią1” i „pamięcią1” oraz między „historią2” a …

pamięćnarracyjnośćselectivityjęzykowy obraz światalinguistic worldviewlanguagingselektywnośćhistoriapodmiotowośćhistoriographymemorynarrationhistoriografiasubjectivityhistoryinterpretacyjnośćujęzykowienieinterpretationEtnolingwistyka
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Designing P-Chirogenic 1,2-Diphosphinobenzenes at Both P-Centers Using P(III)-Phosphinites

2016

International audience; A new enantiodivergent synthesis of P-chirogenic 1,2-diphosphinobenzenes (DP*B) bearing the chirality on one or both phosphorus centers is reported using aryne chemistry. The principle is based on successive reactions of 1,2-dibromobenzene with sec-phosphide boranes, then DABCO to remove the borane, and finally with chlorophosphines or P(III)-chirogenic phosphinites. The efficiency of this synthesis was demonstrated by the stereoselective preparation of (S,S)-1,2-bis(o-anisylphenylphosphino)benzene. A comparison of DIPAMP and homochiral DP*B ligands in asymmetric Rh- or Pd-catalyzed reactions was reported.

phosphine-ligandsDIPAMPketonesStereochemistryBoranesDABCOBorane010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryArynecatalyzed asymmetric hydrogenationchemistry.chemical_compoundfunctionalized alkenes[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesorganocatalysisPhysical and Theoretical Chemistryhydroformylation010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycarbon-monoxide0104 chemical scienceshighly enantioselective hydrogenationOrganocatalysisderivativesStereoselectivityChirality (chemistry)phospholane ligands
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