Search results for "SYNTHESIS"

showing 10 items of 2844 documents

Cyclocarbonylation reactions of allylphenols and allylnaphthols catalyzed by Pd/C- 1,4-bis(diphenylphosphine)butane

2002

Palladium/activated carbon (Pd/C) in the presence of 1,4-bis(diphenylphosphino)butane is an efficient heterogeneous catalyst for cyclocarbonylation reactions of 2-allyl phenols affording five-, six-, and seven-membered ring lactones. Various examples of cyclocarbonylation are reported and the regioselectivity is compared with the homogeneous system. Both commercial Pd/C and Pd/C prepared from activated carbons obtained from vegetable and polymeric wastes are investigated.

Diphenylphosphinechemistry.chemical_elementRegioselectivityButaneGeneral ChemistryHeterogeneous catalysisChemical synthesisCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryOrganic chemistryCarbonylationPalladiumApplied Organometallic Chemistry
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Urīnskābes reakcija ar etiķskābes anhidrīdu: diplomdarbs

1937

DiplomdarbiUrīnskābe:NATURAL SCIENCES::Chemistry::Organic chemistry::Organic synthesis [Research Subject Categories]Ķīmiskās reakcijasAcetic acidUric acidEtiķskābe
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Performance of Spectral Fitting Methods for vegetation fluorescence quantification

2010

The Fraunhofer Line Discriminator (FLD) principle has long been considered as the reference method to quantify solar-induced chlorophyll fluorescence (F) from passive remote sensing measurements. Recently, alternative retrieval algorithms based on the spectral fitting of hyperspectral radiance observations, Spectral Fitting Methods (SFMs), have been proposed. The aim of this manuscript is to investigate the performance of such algorithms and to provide relevant information regarding their use. FLD and SFMs were used to estimate F starting from Top Of Canopy (TOC) fluxes at very high spectral resolution (0.12 nm) and sampling interval (0.1 nm), exploiting the O2-B (687.0 nm) and O2-A (760.6 …

DiscriminatorreflectanceHyperspectral remote sensingSolar-induced chlorophyll fluorescenceMETIS-304492Soil Science550 - Earth sciencesFraunhofer Line Discriminatorin-vivoNoise (electronics)Spectral lineRadiative transfer simulationLaboratory of Geo-information Science and Remote SensingSampling (signal processing)luminescenceLaboratorium voor Geo-informatiekunde en Remote Sensinginduced chlorophyll fluorescenceComputers in Earth SciencesSpectral resolutionMathematicsRemote sensingcanopymodelphotosynthesisscatteringairborneHyperspectral imagingGeologySpectral Fitting MethodPE&RCAGR/14 - PEDOLOGIASpectroradiometerspectroradiometerRadianceREMOTE SENSING OF ENVIRONMENT
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Metal Displacement Deposition: a facile via to grow metal and metal oxide nanostructures

2010

Nanostructured materials have received increasing attention because of their high chemical reactivity that allows an extensive use in many fields, like catalysis, electrosynthesis, sensors, and so on [1]. Taking into account that size plays a fundamental role for the properties of nanostructures, it is of relevant importance for their applications to develop a facile method of synthesis. In our previous works, we have described a template synthesis of metal nanowires through a simple novel route [2-4]. In particular, using a combination of template deposition and metal displacement reaction, we have fabricated pure metal nanowires with a well-defined morphology. This type of template synthe…

Displacement DepositionSettore ING-IND/23 - Chimica Fisica ApplicataMetal Oxide nanostructureMetal nanostructureTemplate Synthesis
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Lanthanum-pyBOX complexes as catalysts for the enantioselective conjugate addition of malonate esters to β,γ-unsaturated α-ketimino esters

2018

[EN] In this paper, we report the application of chiral complexes of La(III) with pyBOX ligands as Lewis acid catalysts in the conjugate addition of malonic esters to N-tosyl imines derived from ß,gamma-unsaturated alfa-keto esters to give the corresponding chiral alfa,ß-dehydroamino esters. pyBOX complexes with La(III), Yb(III), Sc(III), and In(III) triflates were assessed in this reaction but only La(III) showed good activity and enantioselectivity, while Yb(III) provided the expected product with low yield and stereoselectivity, and the Sc(III) and In(III) complexes were completely inactive. The complex of La(OTf)3 with the diphenyl-pyBOX ligand prepared in situ provided the best results…

Double bondEnantioselectivity010402 general chemistry01 natural sciencesMedicinal chemistrychemistry.chemical_compoundCatàlisiMichael additionAsymmetric catalysisMaterials ChemistryLewis acids and basesPhysical and Theoretical Chemistrychemistry.chemical_classification010405 organic chemistryDiastereomerEnantioselective synthesisLanthanide complexes0104 chemical sciencesMalonatechemistryFISICA APLICADAMichael reactionStereoselectivityEnantiomerQuímica orgànica
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Catalytic Asymmetric Formal [3+2] Cycloaddition of 2-Isocyanatomalonate Esters and Unsaturated Imines: Synthesis of Highly Substituted Chiral γ-Lacta…

2017

[EN] Unlike their isocyano and isothiocyanato analogues, isocyanato esters remain almost unexplored as formal 1,3-dipoles in asymmetric catalytic reactions. The first asymmetric formal [3+2] cycloaddition involving isocyanato esters and electrophilic alkenes is reported. Diisopropyl 2-isocyanatomalonate reacts with a,b-unsaturated N-(o-anisidyl) imines in the presence of a Mg(OTf)2¿BOX complex to give highly substituted chiral pyrrolidinones featuring a conjugate exocyclic double bond with excellent yields and enantiomeric excesses up to 99%. Several transformations of the resulting heterocycles, including the synthesis of a pyroglutamic acid derivative, have been carried out.

Double bondLactamsStereochemistryMolecular ConformationStereoisomerismEnantioselectivityAlkenes010402 general chemistryCrystallography X-Ray01 natural sciencesCatalysisCatàlisiCoordination ComplexesAsymmetric catalysisMagnesiumPyrrolidinoneschemistry.chemical_classificationNucleophilic additionCycloaddition Reaction010405 organic chemistryNitrogen heterocyclesOrganic ChemistryEnantioselective synthesisEstersStereoisomerismGeneral ChemistryCycloadditionMalonates0104 chemical scienceschemistryFISICA APLICADAElectrophileIminesEnantiomerNucleophilic additionQuímica orgànicaIsocyanatesChemistry (Weinheim an der Bergstrasse, Germany)
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Syntheses and catalytic oxotransfer activities of oxo molybdenum(vi) complexes of a new aminoalcohol phenolate ligand.

2017

The new aminoalcohol phenol 2,4-di-tert-butyl-6-(((2-hydroxy-2-phenylethyl)amino)methyl)phenol (H2L) was prepared by a facile solvent-free synthesis and used as a tridentate ligand for new cis-dioxomolybdenum(vi)(L) complexes. In the presence of a coordinating solvent (DMSO, MeOH, pyridine), the complexes crystallise as monomeric solvent adducts while in the absence of such molecules, a trimer with asymmetric Mo[double bond, length as m-dash]O→Mo bridges crystallises. The complexes can catalyse epoxidation of cis-cyclooctene and sulfoxidation of methyl-p-tolylsulfide, using tert-butyl hydroperoxide as oxidant.

Double bondTrimer010402 general chemistry01 natural sciencesMedicinal chemistrycatalystsCatalysisAdductInorganic Chemistrychemistry.chemical_compoundkatalyytitmolybdenumPyridineOrganic chemistrycoordination complexesta116chemistry.chemical_classificationkemiallinen synteesi010405 organic chemistryLigandkompleksiyhdisteet0104 chemical sciencesSolventMonomerchemistrymolybdeenichemical synthesisDalton transactions (Cambridge, England : 2003)
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Synthesis and gas chromatographic-mass spectrometric analysis of reduced compounds derived from 6 alpha- and 6 beta-hydroxy-11-deoxycorticosterone.

1989

Abstract A series of thirty two 6-hydroxylated steroids were synthesized by selective reduction of the 4–5 double bond, the 3-oxo group, and/or the 20-oxo group of 6α- and 6β-hydroxyDOC. The different reactions leading to the production of specific isomers are discussed. The gas chromatographic and spectrometric characteristics of the methoxime-trimethylsilyl (MO-TMS) or trimethylsilyl (TMS) derivatives of the isomers obtained are given. The gas chromatographic separation of the syn- and anti -isomers of the methoxime in position 3 was found to be characteristic of the configuration of the hydroxyl in position 6. The difference between methylene unit values of syn- and anti- isomers is much…

Double bondTrimethylsilylChemical PhenomenaClinical BiochemistrySubstituentMass spectrometryBiochemistryChemical synthesisGas Chromatography-Mass Spectrometrychemistry.chemical_compoundEndocrinologyOrganic chemistrySelective reductionMethyleneDesoxycorticosteroneMolecular BiologyPharmacologychemistry.chemical_classificationChromatographyOrganic ChemistryStereoisomerismChemistrychemistrySteroidsGas chromatographyOxidation-ReductionSteroids
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Preemptive analgesia-related gene and protein expression in third molar surgeries under non steroidal anti-inflammatory drug protocols : A PROSPERO-r…

2018

Background This study aimed to review translational studies focusing on third molar removal surgeries through a systematic analytical approach. Material and Methods A PROSPERO-registered systematic review (CRD42017060455) was conducted following the PRISMA statement to summarize current knowledge on gene expression in third molar surgeries. A search was performed in PubMed’s Medline and Scopus databases, without date or language restrictions, using the logical expression {[(Third molar) OR (preemptive) OR (cyclooxygenase inhibitors) OR (acute inflammation) AND (gene expression)]}. Results All studies included in the analysis evaluated gene expression in a third molar extraction model, using…

DrugGene isoformMolarmedia_common.quotation_subjectMEDLINEGene ExpressionReviewBioinformatics03 medical and health sciences0302 clinical medicineText miningGene expressionBiopsyMedicineHumans030212 general & internal medicineGeneral Dentistrymedia_commonmedicine.diagnostic_testbusiness.industryAnti-Inflammatory Agents Non-Steroidal030206 dentistry:CIENCIAS MÉDICAS [UNESCO]TransudateOtorhinolaryngologyProstaglandin-Endoperoxide SynthasesProtein BiosynthesisUNESCO::CIENCIAS MÉDICASSurgeryMolar ThirdAnalgesiaOral Surgerybusiness
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Microseparation techniques for the study of the enantioselectivity of drug-plasma protein binding.

2009

Stereoselectivity in protein binding can have a significant effect on the pharmacokinetic and pharmacodynamic properties of chiral drugs. The investigation of enantioselectivity of drugs in their binding with human plasma proteins and the identification of the molecular mechanisms involved in the stereodiscrimination by the proteins represent a great challenge for clinical pharmacology. In this review, the separation techniques used for enantioselective protein binding experiments are described and compared. An overview of studies on enantiomer–protein interactions, enantiomer–enantiomer interactions as well as chiral drug–drug interactions, including allosteric effects, is presented. The c…

Drugmedia_common.quotation_subjectClinical BiochemistryAllosteric regulationPlasma protein bindingBiochemistryChromatography AffinityAnalytical ChemistryPharmacokineticsSpecies SpecificityDrug DiscoveryHumansAnimal speciesMolecular Biologymedia_commonPharmacologyChromatographyChemistryEnantioselective synthesisElectrophoresis CapillaryStereoisomerismGeneral MedicineBlood ProteinsBlood proteinsPharmaceutical PreparationsChromatography GelStereoselectivityAllosteric SiteProtein BindingBiomedical chromatography : BMC
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