Search results for "chiral"

showing 10 items of 752 documents

Chiral donor–π-acceptor azobenzene dyes

2009

Abstract Four chiral donor–π-acceptor azobenzene dye conjugates were synthesized and characterized. Chiral moieties, namely (S)-(+)-2-(6-methoxy-2-naphthyl)propionic acid (naproxen) and (S)-2-aminopropionic acid ( l -alanine), were attached to either the donor end or the acceptor site of the azo compound using ester or amide bonds, respectively. The structures of the molecules were verified using 1H NMR, 13C NMR and ESI TOF mass spectrometry; spectral properties were evaluated with UV–vis and CD spectrometry whilst thermal stability was determined by TGA. The compounds displayed a broad absorption maximum in the visible region between 433 and 483 nm. All compounds showed relatively high the…

Azo compoundProcess Chemistry and TechnologyGeneral Chemical EngineeringCarbon-13 NMRPhotochemistryAcceptorchemistry.chemical_compoundchemistryAzobenzenePolymer chemistryProton NMRMoleculeThermal stabilityChirality (chemistry)Dyes and Pigments
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Asymmetric Michael Addition in Synthesis of β-Substituted GABA Derivatives

2022

γ-Aminobutyric acid (GABA) represents one of the most prolific structural units widely used in the design of modern pharmaceuticals. For example, β-substituted GABA derivatives are found in numerous neurological drugs, such as baclofen, phenibut, tolibut, pregabalin, phenylpiracetam, brivaracetam, and rolipram, to mention just a few. In this review, we critically discuss the literature data reported on the preparation of substituted GABA derivatives using the Michael addition reaction as a key synthetic transformation. Special attention is paid to asymmetric methods featuring synthetically useful stereochemical outcomes and operational simplicity. This research was funded by the National Na…

Baclofenasymmetric Michael additionγ-aminobutyric-acid derivativesOrganic ChemistryPregabalinPharmaceutical ScienceStereoisomerismQuímica farmacèuticapharmaceuticalsneurological drugsAnalytical ChemistryReaccions químiqueschiral auxiliariesChemistry (miscellaneous)Drug DiscoveryMolecular Medicineenantioselective organocatalysisPhysical and Theoretical Chemistrygamma-Aminobutyric AcidMedicaments
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On-surface Synthesis of a Chiral Graphene Nanoribbon with Mixed Edge Structure.

2020

Abstract Chiral graphene nanoribbons represent an important class of graphene nanomaterials with varying combinations of armchair and zigzag edges conferring them unique structure‐dependent electronic properties. Here, we describe the on‐surface synthesis of an unprecedented cove‐edge chiral GNR with a benzo‐fused backbone on a Au(111) surface using 2,6‐dibromo‐1,5‐diphenylnaphthalene as precursor. The initial precursor self‐assembly and the formation of the chiral GNRs upon annealing are revealed, along with a relatively small electronic bandgap of approximately 1.6 eV, by scanning tunnelling microscopy and spectroscopy.

Band gapAnnealing (metallurgy)530 Physics010402 general chemistry01 natural sciencesBiochemistrygraphene nanoribbonNanomaterialslaw.inventionlawchiral edge540 Chemistrypolycyclic aromatic hydrocarbonon-surface synthesisSpectroscopyQuantum tunnelling010405 organic chemistryChemistryGraphenescanning tunneling microscopy and spectroscopyCommunicationOrganic ChemistryGeneral ChemistryCommunications0104 chemical sciencesZigzagChemical physics570 Life sciences; biologyGraphene nanoribbonsChemistry, an Asian journal
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Erratum to: “Low lying S=−1 excited baryons and chiral symmetry”

2002

BaryonPhysicsChiral symmetryNuclear and High Energy PhysicsExcited stateQuantum mechanicsLyingPhysics Letters B
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The role of the $\Delta(1232)$-resonance in covariant baryon chiral perturbation theory

2013

We stress, on theoretical and phenomenological grounds, the importance of the $\Delta(1232)$-resonance in a chiral effective field theory approach applied to the study of $\pi N$ scattering. We show how its inclusion as a dynamical degree of freedom allow us to obtain reliably valuable information from $\pi N$ scattering data.

BaryonPhysicsElastic scatteringHigh Energy Physics - PhenomenologyChiral perturbation theoryNuclear TheoryScatteringEffective field theoryCovariant transformationCovarianceResonance (particle physics)Mathematical physics
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Pion photo- and electro-production and the chiral MAID interface

2016

We discuss the extended on-mass-shell scheme for manifestly Lorentz-invariant baryon chiral perturbation theory. We present a calculation of pion photo- and electroproduction up to and including order q 4 . The low-energy constants have been fixed by fitting experimental data in all available reaction channels. Our results can be accessed via a web interface, the so-called chiral MAID (http://www.kph.uni-mainz.de/MAID/chiralmaid/). We explain how our program works and how it can be used for further analysis.

BaryonPhysicsParticle physicsChiral perturbation theoryPionInterface (Java)Nuclear TheoryNuclear ExperimentProceedings of The 8th International Workshop on Chiral Dynamics — PoS(CD15)
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Including theΔ(1232)resonance in baryon chiral perturbation theory

2005

Baryon chiral perturbation theory with explicit $\ensuremath{\Delta}(1232)$ degrees of freedom is considered. The most general interactions of pions, nucleons, and \ensuremath{\Delta} consistent with all underlying symmetries as well as with the constraint structure of higher-spin fields are constructed. By use of the extended on-mass-shell renormalization scheme, a manifestly Lorentz-invariant effective-field theory with a systematic power counting is obtained. As applications, we discuss the mass of the nucleon, the pion-nucleon \ensuremath{\sigma} term, and the pole of the \ensuremath{\Delta} propagator.

BaryonPhysicsRenormalizationNuclear and High Energy PhysicsParticle physicsChiral perturbation theoryPionNuclear TheoryPropagatorPerturbation theoryQuantum field theoryNuclear ExperimentNucleonPhysical Review C
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Supramolecular Polymers: Flexible Chirality in Self-Assembled N -Annulated Perylenedicarboxamides (Small 20/2017)

2017

BiomaterialsSupramolecular polymerschemistry.chemical_classificationCircular dichroismCrystallographyMaterials scienceConvective flowchemistryGeneral Materials ScienceGeneral ChemistryChirality (chemistry)BiotechnologySelf assembledSmall
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Insight into the mechanism of diazocompounds transformation catalyzed by hetero cuboidal clusters [Mo3CuQ4(MeBPE)3X4]+, (Q=S, Se; X=Cl, Br): The cata…

2008

Abstract Two enantiomerically pure trinuclear compounds of formula (P)-[Mo3S4{(R,R)-Me–BPE}3Br3]Br and (P)-[Mo3Se4{(R,R)-Me–BPE}3Cl3]Cl, (P)-1b.Br and (P)-1c.Cl, respectively, have been synthesized in a good yield and a stereospecific manner by excision of polymeric [Mo3Q7X4]n (Q = S or Se, X = Cl or Br) phases with (R,R)-Me–BPE{1,2-bis[(2R,5R)-2,5-(dimethylphospholan-1-yl)]ethane}. They have been transformed into chiral hetereo cuboidal compounds [Mo3S4{(R,R)-Me–BPE}3Br3]PF6, (P)-2b.PF6, and [Mo3Se4{(R,R)-Me–BPE}3Cl3]PF6, (P)-2c.PF6, by reaction with copper salts. All these compounds have been characterized by 31P NMR, IR, UV–Vis, mass spectrometry, elemental analysis, and chiral dichroism…

BromineCarbene dimerizationCyclopropanationStereochemistryCyclopropanationOrganic ChemistryPhosphanechemistry.chemical_elementChalcogeneBiochemistryMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundStereospecificitychemistryEthyl diazoacetateChiralYield (chemistry)Materials ChemistryPhysical and Theoretical ChemistryDiazo esterCopperDerivative (chemistry)Journal of Organometallic Chemistry
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Tetrazola hemiamināls kā hirāla palīggrupa

2017

Tetrazola hemiamināls kā hirāla palīggrupa. Sējējs M., zinātniskais vadītājs Prof., Dr. chem. Sūna E., konsultēja MSc. chem., Kinēns A. Maģistra darbs uzrakstīts latviešu valodā, tā apjoms 58 lapaspuses. Darbs satur 56 attēlus, 5 tabulas. Maģistra darbs veltīts terazolu hemiaminālu hirālās palīggrupas iegūšanai un pielietojumam diastereoselektīvajā sintēzē. Izstrādātās hirālās palīggrupas efektivitāte demonstrēta, ar augstu diastereoselektivitāti veicot karbonskābju α-pozīcijas fluorēšanas un nitrozo-aldola reakcijas. Darba rezultātā izstrādāts tetrazola hemiamināla hirālās palīggrupas stereoindukcijas modelis. Demonstrēta hirālās palīggrupas šķelšana maigos reakcijas apstākļos. Tetrazola h…

CHIRAL AUXILIARYENOLATE E/Z ISOMERSTETRAZOLE HEMIAMINALDINAMIC KINETIC RESOLUTIONĶīmija
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