Search results for "lcsh:Organic chemistry"

showing 10 items of 438 documents

Janus Nanostructures from ABC/B Triblock Terpolymer Blends

2019

Lamella-forming ABC triblock terpolymers are convenient building blocks for the synthesis of soft Janus nanoparticles (JNPs) by crosslinking the B domain that is &ldquo

bulk morphologiestechnology industry and agricultureChemiemacromolecular substancesArticlelcsh:QD241-441block copolymersForschungszentren » Center for Nanointegration Duisburg-Essen (CENIDE)lcsh:Organic chemistryddc:540DPD simulationspolymer blendingddc:541Janus nanostructuresFakultät für Chemie » Physikalische ChemiePolymers
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Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics

2012

The preparation of low-generation dendrimers based on a simple calix[4]arene scaffold by insertion of the iminosugar-analogue C2-symmetric 3,4-dihydroxypyrrolidine is described. This methodology allows a rapid incorporation of a considerable number of iminosugar-like moieties in a reduced volume and in a well-defined geometry. The inclusion of alkali-metal ions (sodium and potassium) in the polar cavity defined by the acetamide moieties at the lower rim of the calixarene was demonstrated, which allows also the rigidification of the dendrimer structure and the iminosugar presentation in the clusters. The combination of the supramolecular properties of calixarenes with the advantage of a dend…

calixarenesLetterOrganic ChemistrySupramolecular chemistryIminosugarmultivalencyCombinatorial chemistryPyrrolidinedendrimerslcsh:QD241-441Chemistrychemistry.chemical_compoundlcsh:Organic chemistrychemistryDendrimerCalixareneiminosugarslcsh:Qlcsh:ScienceAcetamidecation-responsive systemBeilstein Journal of Organic Chemistry
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Hyper-reticulated calixarene polymers: a new example of entirely synthetic nanosponge materials

2018

New calixarene-based nanosponges (CaNSs), i.e., hyper-reticulated polymers constituted by calixarene monomer units joined by means of bis(1,2,3-trialzolyl)alkyl linkers, were synthesized, characterized and subjected to preliminary tests to assess their supramolecular absorption abilities towards a set of suitable organic guests, selected as pollutant models. The synthesis was accomplished by means of a CuAAC reaction between a tetrakis(propargyloxy)calix[4]arene and an alkyl diazide. The formation of the polymeric network was assessed by means of FTIR and 13C{1H} CP-MAS solid-state NMR techniques, whereas morphological characterization was provided by SEM microghaphy. The materials were pro…

calixarenesSupramolecular chemistrynanosponges02 engineering and technology010402 general chemistryNanosponge01 natural sciencesFull Research PaperHydrophobic effectlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrySmart materialCalixarenePolymer chemistryFourier transform infrared spectroscopylcsh:ScienceAlkylSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationOrganic ChemistrySettore CHIM/06 - Chimica OrganicaSettore CHIM/05 - Scienza E Tecnologia Dei Materiali PolimericiPolymer021001 nanoscience & nanotechnology0104 chemical sciencesChemistryMonomerchemistrySolid-state nuclear magnetic resonancesmart materialsCalixarenesolid-state NMRlcsh:Q0210 nano-technologyBeilstein Journal of Organic Chemistry
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Polyaminoazide mixtures for the synthesis of pH-responsive calixarene nanosponges

2019

Two mixtures of polyaminoazides were synthesized by a nucleophilic displacement strategy providing no separation of the components. The mixtures were adequately characterized by means of combined HR-ESIMS, FTIR and NMR techniques and, despite their complexity, they were successfully used to accomplish the subsequent preparation of pH-sensitive calixarene hyper-reticulated nanosponge materials. The desired responsivity to pH variations of the nanosponges obtained was verified by means of absorption tests on a set of organic pollutant model molecules.

calixarenesnanosponges02 engineering and technology010402 general chemistry01 natural sciencesFull Research Paperlcsh:QD241-441Nucleophilepolyaminoazideslcsh:Organic chemistryNanospongesCalixareneMoleculeFourier transform infrared spectroscopylcsh:ScienceChemistryOrganic ChemistrypH-responsive materials021001 nanoscience & nanotechnologypH-responsive material0104 chemical sciencesChemistryChemical engineeringpollutantscalixarenepollutantlcsh:QAbsorption (chemistry)0210 nano-technologynanospongeBeilstein Journal of Organic Chemistry
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Analysis of Contact Traces of Cannabis by In-Tube Solid-Phase Microextraction Coupled to Nanoliquid Chromatography

2018

Because of its inherent qualities, in-tube solid-phase microextraction (IT-SPME) coupled on-line to nanoliquid chromatography (nanoLC) can be a very powerful tool to address the new challenges of analytical laboratories such as the analysis of traces of complex samples. This is the case of the detection of contact traces of drugs, especially cannabis. The main difficulties encountered in the analysis of traces of cannabis plants on surfaces are the low amount of sample available (typically &lt

cannabisTHCmedicine.medical_treatmentSample (material)nanoliquid chromatography (nanoLC)CannabinolPharmaceutical Sciencecontact trace analysisSolid-phase microextraction01 natural sciencesArticleGas Chromatography-Mass SpectrometryAnalytical Chemistrylcsh:QD241-441Matrix (chemical analysis)03 medical and health scienceschemistry.chemical_compound0302 clinical medicinelcsh:Organic chemistryDrug DiscoverymedicineCannabidiolNanotechnology030216 legal & forensic medicineDronabinolPhysical and Theoretical ChemistrySolid Phase MicroextractionChromatographybiologyChemistryCannabinoidsPlant Extracts010401 analytical chemistryOrganic ChemistryExtraction (chemistry)biology.organism_classification0104 chemical sciencesChemistry (miscellaneous)CannabinolMolecular MedicineCannabinoidCannabisCannabidiolmedicine.drugin-tube solid-phase microextraction (IT-SPME)Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
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Electrosynthesis and electrochemistry

2015

Since the pioneering work of Kolbe, electrochemistry and electrosynthetic methods have been a part of the repertoire of the organic synthesis toolbox [1–2]. In general, only electrons are employed as reagents or the reagents are electrochemically regenerated. Consequently, waste can be avoided, and limited resources can be used in a careful and economic manner. Because alternative reaction pathways are employed by electrosynthetic methods, scarce and toxic elements can be replaced or are not required at all [3]. Moreover, in the foreseeable future regenerative sources of electricity, for example, photovoltaics and wind power, will provide a surplus of electricity as the current unsteady sup…

chemical methodComputer sciencebusiness.industryOrganic ChemistryThe RenaissanceNanotechnologyElectrosynthesisElectrochemistrysustainabilitylcsh:QD241-441ChemistryEditorialelectrosynthesiselectrochemistrylcsh:Organic chemistryPhotovoltaicslcsh:QElectric powerbusinesslcsh:ScienceLimited resourcesBeilstein Journal of Organic Chemistry
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SF002-96-1, a new drimane sesquiterpene lactone from an Aspergillus species, inhibits survivin expression

2013

Survivin, a member of the IAP (inhibitor of apoptosis) gene family, is overexpressed in virtually all human cancers and is functionally involved in the inhibition of apoptosis, regulation of cell proliferation, metastasis and resistance to therapy. Because of its upregulation in malignancy, survivin has currently attracting considerable interest as a new target for anticancer therapy. In a screening of approximately 200 strains of imperfect fungi for the production of inhibitors of survivin promoter activity, a new drimane sesquiterpene lactone, SF002-96-1, was isolated from fermentations of an Aspergillus species. The compound inhibited survivin promoter activity in transiently transfected…

chemistry.chemical_classificationCell growthnatural productsOrganic Chemistrystructure elucidationapoptosisTransfectionsecondary metabolitesurvivinInhibitor of apoptosisSesquiterpene lactoneMolecular biologyFull Research Paperinhibitorlcsh:QD241-441ChemistrychemistryDownregulation and upregulationlcsh:Organic chemistryApoptosisSurvivinImmunologyProtein biosynthesislcsh:Qlcsh:ScienceBeilstein Journal of Organic Chemistry
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Clicked and long spaced galactosyl- and lactosylcalix[4]arenes: New multivalent galectin-3 ligands

2014

Four novel calix[4]arene-based glycoclusters were synthesized by conjugating the saccharide units to the macrocyclic scaffold using the CuAAC reaction and using long and hydrophilic ethylene glycol spacers. Initially, two galactosylcalix[4]arenes were prepared starting from saccharide units and calixarene cores which differ in the relative dispositions of the alkyne and azido groups. Once the most convenient synthetic pathway was selected, two further lactosylcalix[4]arenes were obtained, one in the cone, the other one in the 1,3-alternate structure. Preliminary studies of the interactions of these novel glycocalixarenes with galectin-3 were carried out by using a lectin-functionalized chip…

chemistry.chemical_classificationChemistrySpecific lectinStereochemistryClick chemistryOrganic ChemistryAlkyneglycocalixarenesFull Research Paperlcsh:QD241-441Chemistrychemistry.chemical_compoundlcsh:Organic chemistrySurface plasmon resonanceCalixareneClick chemistryMultivalencyCluster glycoside effectlcsh:QSurface plasmon resonancelcsh:ScienceEthylene glycolGlycocalixarene
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Pauson–Khand reaction of fluorinated compounds

2020

The Pauson–Khand reaction (PKR) is one of the key methods for the construction of cyclopentenone derivatives, which can in turn undergo diverse chemical transformations to yield more complex biologically active molecules. Despite the increasing availability of fluorinated building blocks and methodologies to incorporate fluorine in compounds with biological interest, there have been few significant advances focused on the fluoro-Pauson–Khand reaction, both in the inter- and intramolecular versions. Furthermore, the use of vinyl fluorides as olefinic counterparts had been completely overlooked. In this review, we collect the advances both on the stoichiometric and catalytic intermolecular an…

chemistry.chemical_classificationCyclopentenoneAlkenealkenePauson–Khand reactionOrganic ChemistryAlkyneReviewCombinatorial chemistryCatalysisenynelcsh:QD241-441Pauson–Khandchemistry.chemical_compoundChemistrylcsh:Organic chemistrychemistryIntramolecular forceYield (chemistry)fluorineMoietyalkynelcsh:Qlcsh:ScienceBeilstein Journal of Organic Chemistry
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Screening of ligands for the Ullmann synthesis of electron-rich diaryl ethers

2012

In the search for new ligands for the Ullmann diaryl ether synthesis, permitting the coupling of electron-rich aryl bromides at relatively low temperatures, 56 structurally diverse multidentate ligands were screened in a model system that uses copper iodide in acetonitrile with potassium phosphate as the base. The ligands differed largely in their performance, but no privileged structural class could be identified.

chemistry.chemical_classificationC–O bond formationDenticityBase (chemistry)catalysisArylOrganic Chemistrynucleophilic aromatic substitutiondiaryl ethersUllmann-type couplingCombinatorial chemistryFull Research PaperCatalysislcsh:QD241-441Chemistrychemistry.chemical_compoundchemistrylcsh:Organic chemistryNucleophilic aromatic substitutionPotassium phosphateOrganic chemistrylcsh:QAcetonitrilelcsh:ScienceCopper iodideBeilstein Journal of Organic Chemistry
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