Search results for "combinatorial"

showing 10 items of 1208 documents

Selective Recognition and Sensing of Succinate vs. Other Aliphatic Dicarboxylates by Thiourea-Functionalized Gold Nanoparticles

2016

Gold nanoparticles functionalized with thiourea moieties have been used as selective colorimetric sensors for the naked-eye detection of succinate versus other aliphatic dicarboxylates, all of them as their TBA salts. The detection process is based on the interparticle aggregation triggered by coordination of the end-carboxylates to the thiourea moieties of two different nanoparticles. This nanoparticle aggregation results in a batochromic shift of the plasmon resonance band and a visual color change from red to blue.

genetic structures010405 organic chemistryNanoparticleGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundThioureachemistrySuccinic acidColloidal goldSurface plasmon resonanceChemistrySelect
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Simple two-step synthesis of 2,4-disubstituted pyrroles and 3,5-disubstituted pyrrole-2-carbonitriles from enones

2014

The cyclocondensation of enones with aminoacetonitrile furnishes 3,4-dihydro-2H-pyrrole-2-carbonitriles which can be readily converted to 2,4-disubstituted pyrroles by microwave-induced dehydrocyanation. Alternatively, oxidation of the intermediates produces 3,5-disubstituted pyrrole-2-carbonitriles.

heterocyclescyclizationOrganic ChemistryTwo stepα-aminonitrilesCombinatorial chemistryFull Research Papermicrowave-assisted synthesislcsh:QD241-441Chemistrychemistry.chemical_compoundchemistrylcsh:Organic chemistrySimple (abstract algebra)pyrrolesAminoacetonitrilelcsh:Qlcsh:SciencePyrroleBeilstein Journal of Organic Chemistry
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An Updated Review on the Synthesis and Antibacterial Activity of Molecular Hybrids and Conjugates Bearing Imidazole Moiety

2020

The rapid growth of serious infections caused by antibiotic resistant bacteria, especially the nosocomial ESKAPE pathogens, has been acknowledged by Governments and scientists and is one of the world’s major health problems. Various strategies have been and are currently investigated and developed to reduce and/or delay the bacterial resistance. One of these strategies regards the design and development of antimicrobial hybrids and conjugates. This unprecedented critical review, in which our continuing interest in the synthesis and evaluation of the bioactivity of imidazole derivatives is testified, aims to summarise and comment on the results obtained from the end of the 1900s until Februa…

imidazoles molecular hybrids molecular conjugates antibacterials antibiotic resistance synthesis bioactivity antibioticsantibiotic resistancesynthesismedicine.drug_classAntibioticsPharmaceutical ScienceReviewMicrobial Sensitivity Tests010402 general chemistry01 natural sciencesantibioticsAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundAntibiotic resistancelcsh:Organic chemistryDrug DiscoveryDrug Resistance BacterialmedicineImidazoleMoietyPhysical and Theoretical Chemistryantibacterialsmolecular conjugatesBacteria010405 organic chemistrymolecular hybridsOrganic ChemistryImidazolesSettore CHIM/06 - Chimica OrganicaBacterial InfectionsAntimicrobialCombinatorial chemistrySettore CHIM/08 - Chimica Farmaceutica0104 chemical sciencesAnti-Bacterial AgentschemistryChemistry (miscellaneous)bioactivityMolecular MedicineAntibacterial activityLinkerConjugateMolecules
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Acylative Dynamic Kinetic Resolution of Secondary Alcohols: Tandem Catalysis by HyperBTM and Bäckvall's Ruthenium Complex.

2021

Non-enzymatic dynamic kinetic resolution (DKR) of secondary alcohols by enantioselective acylation using an isothiourea-derived HyperBTM catalyst and racemization of slowly reacting alcohol by Backvall's ruthenium complex is reported. The DKR approach features high enantioselectivities (up to 99:1), employs easy-to-handle crystalline 4-nitrophenyl isobutyrate as the acylating reagent, and proceeds at room temperature and under an ambient atmosphere. The stereoinduction model featuring cation-π system interactions between the acylated HyperBTM catalyst and π electrons of an alcohol aryl subunit has been elaborated by DFT calculations.

inorganic chemicals010405 organic chemistryArylOrganic ChemistryEnantioselective synthesischemistry.chemical_elementStereoisomerism010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisRuthenium0104 chemical sciencesRutheniumCatalysisKinetic resolutionAcylationchemistry.chemical_compoundKineticschemistryReagentAlcoholsRacemizationThe Journal of organic chemistry
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Mechanism of sulfur transfer across protein-protein interfaces: The cysteine desulfurase model system

2016

CsdA cysteine desulfurase (the sulfur donor) and the CsdE sulfur acceptor are involved in biological sulfur trafficking and in iron-sulfur cluster assembly in the model bacterium Escherichia coli. CsdA and CsdE form a stable complex through a polar interface that includes CsdA Cys328 and CsdE Cys61, the two residues known to be involved in the sulfur transfer reaction. Although mechanisms for the transfer of a sulfur moiety across protein-protein interfaces have been proposed based on the IscS-IscU and IscS-TusA structures, the flexibility of the catalytic cysteine loops involved has precluded a high resolution view of the active-site geometry and chemical environment for sulfur transfer. H…

inorganic chemicals0301 basic medicineChemistryCysteine desulfuraseInorganic chemistrychemistry.chemical_elementIsothermal titration calorimetryGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryAcceptorSulfurCatalysis0104 chemical sciences03 medical and health sciences030104 developmental biologyMoietyTransferaseBiogenesisCysteine
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A solvent-free regioselective iodination route of ortho-carboranes.

2006

Tetraiodo-ortho-carborane based X-ray contrast agents can be readily prepared in a high yield, fast, clean, regioselective fashion by a solvent-free reaction of ortho-carboranes with iodine in sealed tubes.

inorganic chemicalsBoron Compoundschemistry.chemical_elementContrast MediaOrganic-reactions010402 general chemistryIodine01 natural sciencesChemical synthesisInorganic ChemistryQUIMICA ANALITICAOrganic chemistryheterocyclic compoundsSolvent freeintegumentary system010405 organic chemistryChemistryorganic chemicalsRegioselectivityHalogenationCombinatorial chemistry0104 chemical sciencesRadiographyChemical-synthesisOrganic reactionYield (chemistry)SolventsbacteriaDerivativesIodineDalton transactions (Cambridge, England : 2003)
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Supported Ionic Liquid Asymmetric Catalysis. A New Method for Chiral Catalysts Recycling. The Case of Proline-Catalyzed Aldol Reaction.

2004

A new method for chiral catalysts recycling, based on the supported ionic liquid asymmetric catalysis concept, has been developed. This concept involves the treatment of a monolayer of covalently attached ionic liquid on the surface of silica gel with additional ionic liquid. These layers serve as the reaction phase in which the homogeneous chiral catalyst is dissolved. As first application of this concept the L-proline-catalyzed aldol reaction has been carried out. Good yields and ee values, comparable with those obtained under homogeneous conditions have been obtained. Moreover, this material shows high regenerability.

inorganic chemicalsChemistrySilica gelorganic chemicalsOrganic ChemistryInorganic chemistryEnantioselective synthesisGeneral MedicineBiochemistryCombinatorial chemistryCatalysischemistry.chemical_compoundAldol reactionCovalent bondPhase (matter)Drug DiscoveryMonolayerIonic liquidChemInform
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2015

One-pot combination of the in-situ generation of hydrogen peroxide (H2O2) with selective oxidation reactions enhances the environmental and economic attractiveness of the use of H2O2 as green oxidant at industrial scale. This tandem reaction improves not only the safety aspects associated to H2O2 storage and transportation but also reduces the capital and operation costs. This review covers the progress in the field focussing on the areas of catalysis development, mechanistic understanding and engineering approaches (such as membrane reactors) for specific systems involving epoxidation of propylene oxide, hydroxylation of benzene, oxygenate synthesis from methane and Fenton processes, highl…

inorganic chemicalsGreen chemistryMembrane reactorGeneral ChemistryCombinatorial chemistryRedoxCatalysisCatalysischemistry.chemical_compoundchemistryCascade reactionOrganic chemistryPropylene oxideHydrogen peroxideOxygenateCatalysis Today
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Recent Advances in Halogen Bonded Assemblies with Resorcin[4]arenes

2020

Resorcinarenes are cavity-containing compounds when in the crown conformation, from the calixarene family of concave compounds. These easy to synthesize macrocycles can be decorated at the upper rim through the eight hydroxyl groups and/or the 2-position of the aromatic ring. They are good synthons in supramolecular chemistry leading to appealing assemblies such as open-inclusion complexes, capsules and tubes through multiple weak interactions with various guests. Halogen bonding (XB) is a highly directional non-covalent interaction by an electron-deficient halogen atom as a donor that interacts with a Lewis base, the XB acceptor. This tutorial review provides an overview of recent advances…

inorganic chemicalsHalogen bond010405 organic chemistryChemistryGeneral Chemical EngineeringSynthonSupramolecular chemistryGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryAcceptorCombinatorial chemistry0104 chemical sciencesCalixareneHalogenMaterials ChemistryLewis acids and basesThe Chemical Record
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Amino-Acid-Based Polymerizable Surfactants for the Synthesis of Chiral Nanoparticles

2016

Amino-acid-based chiral surfactants with polymerizable moieties are synthesized, and a versatile approach to prepare particles thereof with a chiral surface functionality is presented. As an example of an application, the synthesized particles are tested for their ability as nucleating agents in the enantioselective crystallization of amino acid conglomerate systems, taking rac-asparagine as a model system. Particles resulting from chiral surfactants with different tail groups are compared and the results demonstrate that only the chiral nanoparticles made of the polymerizable surfactant are able to act efficiently as nucleation agent in enantioselective crystallization.

inorganic chemicalsMaterials sciencePolymers and PlasticsPolymersNucleationNanoparticleModel system02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationlaw.inventionSurface-Active AgentsPulmonary surfactantlawMaterials ChemistryOrganic chemistryAmino AcidsCrystallizationchemistry.chemical_classificationMolecular Structureorganic chemicalsOrganic Chemistrytechnology industry and agricultureEnantioselective synthesisStereoisomerism021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesAmino acidchemistryNanoparticles0210 nano-technologyChirality (chemistry)Macromolecular Rapid Communications
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