Search results for "Planar chirality"

showing 5 items of 5 documents

Enantioselective Strecker Reaction Catalyzed by an Organocatalyst Lacking a Hydrogen-Bond-Donor Function

2007

Hydrogen bondChemistryOrganocatalysisStrecker amino acid synthesisEnantioselective synthesisOrganic chemistryGeneral ChemistryPlanar chiralityCatalysisCatalysisAngewandte Chemie International Edition
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Chiral Self‐Sorting of trans ‐Chelating Chiral Ligands upon Formation of Pd II Complexes (Eur. J. Inorg. Chem. 15/2014)

2014

Inorganic ChemistrySelf sortingchemistryStereochemistryPolymer chemistrySupramolecular chemistrychemistry.chemical_elementChelationSelf-assemblyPlanar chiralityPalladiumEuropean Journal of Inorganic Chemistry
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Comparative enantioseparation of planar chiral ferrocenes on polysaccharide‐based chiral stationary phases

2022

Planar chiral ferrocenes are well-known compounds that have attracted interest for application in synthesis, catalysis, material science, and medicinal chemistry for several decades. In spite of the fact that asymmetric synthesis procedures for obtaining enantiomerically enriched ferrocenes are available, sometimes, the accessible enantiomeric excess of the chiral products is unsatisfactory. In such cases and for resolution of racemic planar chiral ferrocenes, enantioselective high-performance liquid chromatography (HPLC) on polysaccharide-based chiral stationary phases (CSPs) has been used in quite a few literature articles. However, although moderate/high enantioselectivities have been ob…

PharmacologyPlanar chiralityMetallocenesElectrostatic potentialelectrostatic potential; enantioseparation; ferrocenes; planar chirality; polysaccharide-based chiral stationary phasesOrganic ChemistryStereoisomerismQuímica analíticaSettore CHIM/06 - Chimica OrganicaPolysaccharide-based chiral stationary phasesCatalysisEnantioseparationAnalytical ChemistryPolysaccharidesDrug DiscoverySettore CHIM/01 - Chimica AnaliticaAmyloseFerrocenesChromatography High Pressure LiquidSpectroscopyChirality
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A general diastereoselective synthesis of highly functionalized ferrocenyl ambiphiles enabled on a large scale by electrochemical purification

2017

International audience; A general synthesis of highly functionalized ferrocenes, which include (P,B)- and (N,B)-ambiphiles, has been developed at a multigram scale. Diastereoselective stepwise modification of di-tert-butylated ferrocenes included the unprecedented separation of electroactive species. Bulky alkyl groups on ferrocenes ensure planar chirality of ambiphiles and enforce closer proximity of antagonist Lewis functions.

catalytic applicationsPlanar chirality010402 general chemistryElectrochemistrycarbon-dioxide01 natural sciences[ CHIM ] Chemical SciencesCatalysisMaterials ChemistryOrganic chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryfree hydrogen activationaryl bromidesAlkylchemistry.chemical_classificationcomplexes010405 organic chemistryChemistryligandsdirect arylationMetals and AlloysGeneral ChemistrypalladiumCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsfrustrated lewis pairsCeramics and Compositescoordination chemistry
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Chiroptical inversion of a planar chiral redox-switchable rotaxane.

2019

Reversible redox-switching of a planar chiral [2]rotaxane with a tetrathiafulvalene-bearing crown ether macrocycle generates a complete sign reversal of the main band in the ECD spectrum, as shown by experiment and rationalised by DFT calculations.

chemistry.chemical_classificationMaterials scienceRotaxane010405 organic chemistryGeneral Chemistry547Planar chirality010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesChiral column chromatographyCrystallographychemistry.chemical_compoundChemistry500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische Chemieredox-switchablechemistryElectronic effectrotaxanechiroptical inversionEnantiomermakromolekyylitTetrathiafulvaleneCrown etherChemical science
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