Search results for "Asymmetric carbon"

showing 6 items of 6 documents

Enantiomeric Resolution of Asymmetric-Carbon-Free Binuclear Double-Stranded Cobalt(III) Helicates and Their Application as Catalysts in Asymmetric Re…

2018

A series of double-stranded binuclear helicates [Co2(H1)2]4+, [Co2(H2)2]4+, and [Co2(H3)2]4+, derived from monodeprotonated bis-pyridyl hydrazine-based ligands of H21, H22, and H23 with one, two, and three -CH2 spacers, were obtained. These asymmetric-carbon-free racemic helicates were separated into their ΔΔ and ΛΛ enantiomers. The resolved helicates were examined for the first time as enantioselective catalysts in asymmetric benzoylation and nitroaldol reactions.

010405 organic chemistryResolution (electron density)HydrazineEnantioselective synthesischiralitychemistry.chemical_elementkompleksiyhdisteet010402 general chemistry01 natural sciencessupramolecular chemistry0104 chemical sciencesCatalysisInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryAsymmetric carbonsupramolekulaarinen kemiacoordination complexesPhysical and Theoretical ChemistryEnantiomerta116CobaltDouble strandedInorganic Chemistry
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Modelling the enantioresolution capability of cellulose tris(3,5-dichlorophenylcarbamate) stationary phase in reversed phase conditions for neutral a…

2018

[EN] To the best of our knowledge, the prediction of the enantioresolution ability of polysaccharides-based stationary phases in liquid chromatography for structurally unrelated compounds has not been previously reported. In this study, structural information of neutral and basic compounds is used to model their enantioresolution levels obtained from an immobilised cellulose tris(3,5-dichlorophenylcarbamate) stationary phase in reversed phase conditions. Thirty-four structurally unrelated chiral drugs and pesticides, from seven families, are studied. Categorical enantioresolution levels (RsC, 0 = no baseline enantioresolution and 1 = baseline enantioresolution) are established from the expe…

Models MolecularTrisPhenylcarbamatesEnantioresolution modelling01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundMolecular descriptorPhase (matter)Tris(35-dichlorophenylcarbamate)MoleculeLeast-Squares AnalysisPesticidesCelluloseCelluloseChromatography High Pressure LiquidReversed phase liquid chromatographyEnantioseparationsChromatography Reverse-PhasePrincipal Component AnalysisChromatography010405 organic chemistry010401 analytical chemistryOrganic ChemistryDiscriminant partial least squaresDiscriminant AnalysisStereoisomerismGeneral MedicineReversed-phase chromatography0104 chemical scienceschemistryStationary phaseAsymmetric carbonStationary phaseJournal of Chromatography A
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Enantioresolution in electrokinetic chromatography-complete filling technique using sulfated gamma-cyclodextrin. Software-free topological anticipati…

2016

Few papers have tried to predict the resolution ability of chiral selectors in capillary electrophoresis for the separation of the enantiomers of chiral compounds. In a previous work, we have used molecular information available on-line to establish enantioresolution levels of basic compounds using highly sulfated β-CD (HS-β-CD) as chiral selector in electrokinetic chromatography-complete filling technique (EKC-CFT). The present study is a continuation of this previous work, introducing some novelties. In this work, the ability of sulfated γ-cyclodextrin (S-γ-CD) as chiral selector in EKC-CFT is modelled for the first time. Thirty-three structurally unrelated cationic and neutral compounds …

Resolution (mass spectrometry)02 engineering and technologyTopology01 natural sciencesBiochemistryAnalytical ChemistryElectrokinetic phenomenaCapillary electrophoresisCationsMoleculeLeast-Squares AnalysisPesticidesTopology (chemistry)Chromatography Micellar Electrokinetic CapillaryChromatographyChemistry010401 analytical chemistryOrganic ChemistryCationic polymerizationDiscriminant AnalysisStereoisomerismGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesPharmaceutical PreparationsAsymmetric carbonIndicators and ReagentsEnantiomer0210 nano-technologySoftwaregamma-CyclodextrinsJournal of Chromatography A
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Allylpalladium( II ) Complexes with Aminophosphane Ligands: Solution Behaviour and X‐ray Structure of cis ‐[Pd(η 3 ‐CH 2 CHCHPh){Ph 2 PCH 2 CHPhNH(2,…

2004

A new β-aminophosphane L2 [Ph2PCH2CH(Ph)NH(2,6-C6H3iPr2)], bearing an asymmetric carbon atom and a vicinal prochiral nitrogen centre and (η3-allyl)palladium complexes of general formula [Pd(η3-C3H4R){η2-Ph2PCH2CH(Ph)NHAr}][PF6] (1−6) (R = H, Me or Ph and Ar = Ph or 2,6-C6H3iPr2) have been synthesised. NMR spectroscopic studies and a crystal structure analysis of complex 6 (R = Ph, Ar = 2,6-C6H3iPr2) confirmed the highly diastereoselective coordination of the nitrogen atom. Because of the allyl fluxionality and the presence of asymmetric centres, all the complexes exist in solution as mixtures of up to four diastereomers. For the monosubstituted allyl complexes [Pd(η3-C3H4R){Ph2PCH2CH(Ph)NHA…

Steric effectsAllylic rearrangement010405 organic chemistryChemistryStereochemistryDiastereomerRegioselectivityCrystal structure010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic ChemistryAsymmetric carbonMoietyIsomerizationEuropean Journal of Inorganic Chemistry
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LC-Polymers with Axial Chirality

1991

Abstract Liquid crystalline polymers with axial chirality are prepared. These polymers are chiral, not due to a single asymmetric carbon atom, but due to a larger molecular fragment, which is chiral as a whole. They exhibit cholesteric and chiral smectic C* phases. Dielectric spectroscopy proves strong ferroelectric properties in the chiral smectic C* phases of these polymers.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceStereochemistryLiquid crystallineHigh Energy Physics::LatticeHigh Energy Physics::PhenomenologyPolymerFerroelectricityDielectric spectroscopyCondensed Matter::Soft Condensed MatterCondensed Matter::Materials ScienceCrystallographychemistryAsymmetric carbonAxial chiralityChirality (chemistry)Molecular Crystals and Liquid Crystals
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Synthesis, crystal structure and Hirshfeld analysis of a crystalline compound comprising a 1/1 mixture of 1-[(1R,4S)- and 1-[(1S,4R)-1,7,7-trimethyl-…

2020

A racemic mixture of (R)- and (S)-camphor thio­semicarbazone, which crystallizes in the centrosymmetric space group C2/c, is reported.

crystal structurechiral thiosemicarbazonechiral thio­semicarbazonecamphor derivativeThio-Crystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesResearch Communicationsracemic mixtureCrystalchemistry.chemical_compoundGroup (periodic table)AmideGeneral Materials ScienceCrystallographyChemistryGeneral ChemistryCondensed Matter Physics0104 chemical sciencesCrystallographyAsymmetric carbonQD901-999Racemic mixtureChirality (chemistry)Acta Crystallographica Section E: Crystallographic Communications
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