Search results for "Microwave irradiation"

showing 10 items of 31 documents

Heterogeneous Sonogashira Coupling over Nanostructured SiliaCat Pd(0)

2012

Sol–gel entrapped catalyst SiliaCat Pd(0) heterogeneously mediates the Sonogoashira coupling of different aryl halides and phenylacetylene either under thermal conditions or, much more efficiently, under microwave irradiation, affording good conversions of coupled products. Leaching of valued Pd is limited, and the catalyst can be reused.

Renewable Energy Sustainability and the EnvironmentHeterogeneouGeneral Chemical EngineeringArylSonogashira couplingHalideSonogashira couplingPd catalysiGeneral ChemistryPhotochemistryCatalysisSiliaCatchemistry.chemical_compoundSol−gelchemistryPhenylacetyleneMicrowave irradiationEnvironmental ChemistryLeaching (metallurgy)Sol-gelACS Sustainable Chemistry & Engineering
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Microwave effects on germination and growth of radish (Raphanus sativus L.) seedlings

2002

Germination of radish seeds was delayed and reduced by low-power microwave exposure at 10.5 and 12.5 GHz. Irradiation decreased also hypocotyl growth rate. These effects were increased by rising of the microwave power and by the vertically polarised electromagnetic field. When the irradiation was suspended the seedling growth recovered.

Settore BIO/01 - Botanica GeneraleRaphanus sativuGerminationSeedling growthMicrowave irradiation
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A novel synthetic approach to pyran-2,4-dione scaffold production: Microwave-assisted dimerization, cyclization, and expeditious regioselective conve…

2020

Abstract Here, we report a novel, green, simple, low-cost, and rapid methodology for the high-yield production of pyran-2,4-dione scaffolds under microwave irradiation. Regio- and stereoselective conversions of β-diketone systems into β-enaminones were achieved using 18 primary amines and four amino acid esters. Microwave-assisted further cyclization of 3-(β-substitutedvinyl)-6-phenyl-pyran-2,4-dione into 3-benzoyl-4,7-diphenyl-2H,5H-pyrano[4,3-b]pyran-2,5-dione via reaction with ethyl benzoyl acetate.

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesBiochemistryMicrowave assistedCombinatorial chemistry0104 chemical sciencesAmino acidchemistry.chemical_compoundchemistryPyranDrug DiscoveryMicrowave irradiationStereoselectivityTetrahedron Letters
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Microwave-assisted synthesis of novel cyclodextrin–cucurbituril complexes

2011

Microwave irradiation was successfully used in order to obtain stable supramolecular aggregates between cyclodextrins and cucurbiturils, without the participation of any long-chain common ‘molecular thread’ guest. These aggregates were characterised by means of various different techniques, namely NMR, thermogravimetry, polarimetry and ESI-MS. Cross-analysis of experimental data allowed us to obtain insights on the stoichiometries of the composites and their thermal stabilities. The possible structures of the composites are briefly discussed, as well as the actual nature of their intrinsic stability.

chemistry.chemical_classificationcyclodextrinsCyclodextrinCUCURBITURILSSupramolecular chemistryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMicrowave assistedcucurbiturilThermogravimetrychemistrycyclodextrinCucurbiturilComputational chemistryMicrowave irradiationOrganic chemistrymicrowave irradiationStoichiometry
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Microwave-Assisted Synthesis of Polysubstituted 4-Quinolones from Deprotonated α-Aminonitriles

2010

The α-alkylation of deprotonated N-aryl-α-aminonitriles with α-bromoesters furnishes intermediates that can be cyclized to 4-quinolones upon microwave irradiation. Alternatively, base-induced dehydrocyanation of the alkylation products furnishes enaminoesters, which can, for example, be converted into quinoline-3-carboxylates.

chemistry.chemical_compoundDeprotonationMicrowave chemistryChemistryOrganic Chemistry4-quinolonesMicrowave irradiationCarboxylatePhysical and Theoretical ChemistryAlkylationPhotochemistryChemical synthesisMicrowaveEuropean Journal of Organic Chemistry
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ChemInform Abstract: Cyclocondensation of α-Aminonitriles and Enones: A Short Access to 3,4-Dihydro-2H-pyrrole 2-Carbonitriles and 2,3,5-Trisubstitut…

2010

The reaction of α,β-unsaturated carbonyl compounds with aminoacetonitrile hydrochloride furnishes 3,5-disubstituted 3,4-dihydro-2H-pyrrole-2-carbonitriles in a one-pot reaction sequence. While these products can serve as starting materials for the preparation of polysubstituted pyrrolizidines, they are kinetically stable against the base-induced elimination of HCN. In contrast, their 2-substituted analogues obtained from α-substituted α-aminonitriles can be readily converted to the corresponding 2,3,5-trisubstituted pyrroles under microwave irradiation. The key step presumably involves the thermal electrocyclization of a stabilized 2-azapentadienyl anion formed by condensation of the reacta…

chemistry.chemical_compoundDeprotonationReaction sequenceChemistryHydrochlorideMicrowave irradiationCondensationAminoacetonitrileGeneral MedicineMedicinal chemistryPyrrole derivativesPyrroleChemInform
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ChemInform Abstract: Green Conditions for the Suzuki Reaction Using Microwave Irradiation and a New HNT-Supported Ionic Liquid-Like Phase (HNT-SILLP)…

2014

Aryl iodides are coupled with conversions comparable to aryl bromides whereas conversions of aryl chlorides are significantly lower.

chemistry.chemical_compoundSuzuki reactionChemistryPhase (matter)ArylMicrowave irradiationIonic liquidGeneral MedicinePhotochemistryCatalysisChemInform
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Simultaneous production of furfural and levulinic acid from pine sawdust via acid-catalysed mechanical depolymerization and microwave irradiation

2019

Abstract In this work pine sawdust was converted into levulinic acid (LA) and furfural. Sawdust was first pre-treated with sulfuric acid-catalysed mechanical depolymerization. The conversion reactions were then performed with microwave heating at 180 °C. To enhance the furfural yield and the efficient separation of furfural and LA, a biphasic water-toluene reaction system was used. The effect of an additional catalyst, AlCl3, on the yield of LA and furfural was also studied. According to the results the pre-treatment method enhanced the yields of LA. In addition, due to the microwave heating the reaction times were short. Additional AlCl3 catalyst enhanced the LA yield, however excellent fu…

mechanical depolymerizationbiomassa020209 energyhapotlevulinic acid02 engineering and technologyFurfuralCatalysismikroaallotchemistry.chemical_compoundBioenergykemian tekniikka0202 electrical engineering electronic engineering information engineeringLevulinic acidta215microwave irradiationWaste Management and Disposalta218orgaaniset yhdisteetacid catalysisbiomassRenewable Energy Sustainability and the EnvironmentDepolymerizationForestryfurfuralchemistryYield (chemistry)visual_artvisual_art.visual_art_mediumSawdustAgronomy and Crop ScienceMicrowavepuu (luonnonmateriaalit)Nuclear chemistryBiomass and Bioenergy
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A methodical 68Ga-labelling study of DO2A-(butyl- l-tyrosine)2 with cation-exchanger post-processed 68Ga: practical aspects of radiolabelling

2011

Positron emission tomography (PET) with 68Ga is a fast-growing field in molecular imaging, both in research and in clinical routine. The availability of 68Ga via the 68Ge/68Ga radionuclide generator facilitates the development and production of radiopharmaceuticals independent of a cyclotron. The presented work shows a complete 68Ga labelling study exemplified on [68Ga]DO2A-(butyl- l-tyrosine)2, a potential tumour tracer for PET. A methodical sequence is followed to optimize the 68Ga-labelling reaction. Practical aspects are described and the different parameters contributing to the labelling yield are demonstrated. The influence of temperature, time, amount of labelling precursor and pH va…

medicine.diagnostic_testIon exchangebusiness.industryChemistryRadiochemistryClinical routinePositron emission tomographyLabellingYield (chemistry)Microwave irradiationmedicineRadiology Nuclear Medicine and imagingRadionuclide GeneratorNuclear medicinebusinessContrast Media & Molecular Imaging
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Application of Molecular Topology for the Prediction of Reaction Yields and Anti-Inflammatory Activity of Heterocyclic Amidine Derivatives

2011

Topological-mathematical models based on multiple linear regression analyses have been built to predict the reaction yields and the anti-inflammatory activity of a set of heterocylic amidine derivatives, synthesized under environmental friendly conditions, using microwave irradiation. Two models with three variables each were selected. The models were validated by cross-validation and randomization tests. The final outcome demonstrates a good agreement between the predicted and experimental results, confirming the robustness of the method. These models also enabled the screening of virtual libraries for new amidine derivatives predicted to show higher values of reaction yields and anti-infl…

multilineal regression analysisQSAR analysisAmidinesAnti-Inflammatory AgentsQuantitative Structure-Activity RelationshipArticleCatalysismolecular topologylcsh:ChemistryInorganic ChemistryAmidineHeterocyclic Compounds 1-Ringchemistry.chemical_compoundComputational chemistryLinear regressionOrganic chemistryPhysical and Theoretical Chemistryyield reactionanti-inflammatory activitylcsh:QH301-705.5Molecular BiologySpectroscopyChemistryOrganic ChemistryGeneral MedicineComputer Science Applicationslcsh:Biology (General)lcsh:QD1-999Microwave irradiationMolecular topologyAlgorithmsamidine derivativesInternational Journal of Molecular Sciences
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