Search results for "selectivity"

showing 10 items of 1148 documents

Identification of a positively evolving putative binding region with increased variability in posttranslational motifs in zonadhesin MAM domain 2.

2005

Positive selection has been shown to be pervasive in sex-related proteins of many metazoan taxa. However, we are only beginning to understand molecular evolutionary processes on the lineage to humans. To elucidate the evolution of proteins involved in human reproduction, we studied the sequence evolution of MAM domains of the sperm-ligand zonadhesin in respect to single amino acid sites, solvent accessibility, and posttranslational modification. GenBank-data were supplemented by new cDNA-sequences of a representative non-human primate panel. Solvent accessibility predictions identified a probably exposed fragment of 30 amino acids belonging to MAM domain 2 (i.e., MAM domain 3 in mouse). The…

GlycosylationGlycosylationMolecular Sequence DataBiologyProtein Serine-Threonine Kinaseschemistry.chemical_compoundMiceN-linked glycosylationGenetic variationGeneticsAnimalsAmino Acid SequenceBinding sitePhosphorylationSelection GeneticMolecular BiologyPeptide sequenceEcology Evolution Behavior and SystematicsBinding selectivitychemistry.chemical_classificationGeneticsBinding SitesBase SequenceSequence Homology Amino AcidGenetic VariationMembrane ProteinsAmino acidRepressor ProteinsSperm MaturationchemistryMultigene FamilyPhosphorylationProtein Processing Post-TranslationalTranscription FactorsMolecular phylogenetics and evolution
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A Universal Approach to Quantify Overpotential-Dependent Selectivity Trends for the Competing Oxygen Evolution and Peroxide Formation Reactions : A C…

2021

In this article, we study the competing oxygen evolution and hydrogen peroxide (H2O2) formation reactions for periodic models of graphene with different active-site concentrations by means of densi...

GrapheneOxygen evolutionChemie02 engineering and technologyOverpotential010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesPeroxide3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundGeneral EnergychemistrylawElectrodePhysical and Theoretical Chemistry0210 nano-technologySelectivityHydrogen peroxide
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Efficient microwave-assisted synthesis of glycerol monodecanoate

2017

International audience; Solvent-free microwave-assisted synthesis was carried out to prepare 2,3-dihydroxypropyl decanoate, by esterification of decanoic acid in the presence of two distinct glycerol derivatives, glycidol, and glycerol carbonate, respectively. The process described is based on microwaves heating source with electrical power in the range of 200–400 W, involving stoichiometric proportions of decanoic acid and glycerol derivatives, and using catalytic amounts of TBAI used as organocatalyst. Conversion and selectivity rates of esterification reactions were monitored by 1H and 13C{1H} NMR spectroscopy. The predominantly formed ester, 2,3-dihydroxypropyl decanoate was fully chara…

Green chemistryBio-based building-blocksGlycerol derivatives02 engineering and technology010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundGlycerolOrganic chemistry[CHIM]Chemical Sciences1-MonoacylglycerolComputingMilieux_MISCELLANEOUSGlycidolGeneral ChemistryDecanoic acidNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnology0104 chemical sciencesMicrowave-assisted organic chemistrychemistryGreen chemistry13. Climate action0210 nano-technologySelectivityStoichiometryFood ScienceBiotechnology
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Ionic liquids as precatalysts in the highly stereoselective conjugate addition of α,β-unsaturated aldehydes to chalcones.

2014

Imidazolium-based ionic liquids (ILs) serve both as recyclable reaction media and as precatalysts for the N-heterocyclic carbene-catalyzed conjugate addition of α,β-unsaturated aldehydes to chalcones. The reaction produces a broad scope of 1,6-ketoesters incorporating an anti-diphenyl moiety in high yields and with high stereoselectivity. In recycling experiments, the IL can be reused up to five times with retained reactivity and selectivity. Moreover, the 1,6-ketoesters form self-assembled organogels in aliphatic hydrocarbons. The reaction protocol is robust, easily operated, scalable and highly functionalized compounds can be obtained from inexpensive and readily accessible starting mater…

Green chemistryChemistryOrganic ChemistryGeneral ChemistryCatalysischemistry.chemical_compoundIonic liquidMoietyOrganic chemistryReactivity (chemistry)StereoselectivitySelectivityta116ConjugateChemistry (Weinheim an der Bergstrasse, Germany)
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Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids

2011

“The best catalyst is no catalyst.” With growing public concern over global warming and the amount of greenhouse gases, it is important to reduce the amount of chemicals and eliminate waste, to obtain better results in a simple, selective, safe, and environmentally benign fashion compared to conventional tedious chemical synthesis. Herein, we disclose an environmentally benign, rapid, catalyst/promoter/coupling reagent-free cyclization procedure of free amino acids to furnish exclusively cyclic dipeptides (2,5-diketopiperazines, DKPs) in excellent or even quantitative yield, along with their solid state self-assembling properties. This process is extremely simple and highly efficient with l…

Green chemistrychemistry.chemical_classificationCyclic compoundChemistryPollutionChemical synthesisCyclic peptideCatalysisSolventYield (chemistry)Environmental ChemistryOrganic chemistrySelectivityta116Green Chemistry
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Syntheses of (+)-alismoxide and (+)-4-epi-alismoxide.

2006

The first total syntheses of (+)-alismoxide and (+)-4-epi-alismoxide are reported. Formal chemo-, regio-, and stereoselective addition of water to 10alpha-acetoxy-1alphaH,5betaH-guaia-3,6-diene afforded the target compounds after reduction. The absolute stereochemistry of (+)-alismoxide has been established. The low [alpha](D) +8.6 value indicates that significant amounts of alismoxide result from biosynthetic processes. Furthermore, the structure of the natural guaienediol isolated from Silphium perfoliatum has been corrected to (-)-alismoxide.

GuaninebiologyMolecular StructureChemistryStereochemistryOrganic ChemistryAbsolute configurationTotal synthesisRegioselectivityWaterStereoisomerismStereoisomerismAsteraceaebiology.organism_classificationChemical synthesisAzulenesSesquiterpenes GuaianeSilphium perfoliatumStereoselectivityChemoselectivityThe Journal of organic chemistry
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Stereoselective Access to Fluorinated and Non-fluorinated Quaternary Piperidines: Synthesis of Pipecolic Acid and Iminosugar Derivatives

2012

The preparation of optically pure quaternary piperidines, both fluorinated and non-fluorinated, has been achieved from a chiral imino lactone derived from (R)-phenylglycinol. In the case of the fluorinated derivatives, the addition of (trifluoromethyl)trimethylsilane (TMSCF(3)) followed by iodoamination and migration of the CF(3) group allowed access to four derivatives of α-(trifluoromethyl)pipecolic acid. A theoretical study of the CF(3)-group rearrangement has been carried out to help establish the reaction mechanism of this uncommon transformation. Moreover, a route to trifluoromethyl-substituted iminosugars was also developed through the diastereoselective dihydroxylation of suitable s…

HalogenationStereochemistryIminosugarAlkylationCatalysischemistry.chemical_compoundPiperidinesfluorineiminosugarsPipecolic acidchemistry.chemical_classificationamino acidsTrifluoromethylMolecular StructureChemistryOrganic ChemistryHalogenationStereoisomerismGeneral ChemistryImino SugarsDihydroxylationPipecolic Acidsdensity functional calculationsquaternary stereocentersStereoselectivityLactone
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AuX3-Mediated Selective Head-to-Head Dimerization of Difluoropropargyl Amides

2009

A dimerization of difluoropropargyl amides by reaction with gold(III) halides is described. A reductive elimination of a divinylgold species can be invoked to rationalize its formation. Initial studies of the unusual reactivity of these 1,4-dihalo-1,3-dienes have been performed.

Head to headStereochemistryChemistrymedicine.drug_classOrganic ChemistrymedicineChemical reductionCarboxamideReactivity (chemistry)SelectivityReductive eliminationThe Journal of Organic Chemistry
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Carbohydrate binding specificity and purification by biospecific affinity chromatography of Ascidiamalaca traust. Hemagglutinins

1982

The carbohydrate specificities of Ascidia malaca serum hemagglutinins were determined by hemagglutination inhibition tests. Analysis of agglutinins against rabbit and human A, B, O erythrocytes suggests that the size of the combining site corresponds to a disaccharide with a specificity for saccharides containing a D-galacto configuration (D-melibiose, D-raffinose, D-galactose, alpha-lactose, lactulose, L-arabinose). No anomeric specificity was observed with oligosaccharides. Hydroxyl groups probably involved in hydrogen-bond formation with agglutinin binding site, were identified as carbons C2, C4, C5 and C6 of D-galactose. Absorption experiments showed that two distinct agglutinins with s…

Hemagglutination Inhibition TestsErythrocytesImmunologyDisaccharideBiologyChromatography Affinitychemistry.chemical_compoundRaffinoseAgglutininSpecies SpecificityAffinity chromatographyAnimalsHumansUrochordataBinding sitePolyacrylamide gel electrophoresisBinding selectivityMelibioseBinding SitesGalactoseHemagglutination TestsHemagglutination Inhibition TestsAgglutination (biology)HemagglutininschemistryBiochemistryAntibody FormationCarbohydrate MetabolismRabbitsDevelopmental BiologyDevelopmental & Comparative Immunology
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The role of pore topology on the behaviour of FCC zeolite additives

1999

Abstract A large variety of zeolite topologies including: large pore tridirectional (Beta), large pore unidirectional (Mordenite, SSZ-24), bidirectional 10 member ring pores (MRP) (ZSM-5), bidirectional 10 × 8 MRP (Ferrierite), tridirectional with connected 12 and 10 MRP (CIT-1), bidirectional with 12 MRP connected by 10 MRP (NU-87), tridirectional with 10 × 11 × 12 MRP (NU-86), and finally 10 MRP, and independent 12 MR cavities connected by 10 MR windows (MCM-22), have been studied as catalysts for the cracking of a gasoline range model molecule ( n -heptane). Kinetic and decay constants as well as selectivity parameters such as paraffin/olefin, i -C 4 / n -C 4 , i -C 5 / n -C 5 , C 3 /C 4…

HeptaneOlefin fiberChemistryProcess Chemistry and TechnologyMineralogyFluid catalytic crackingMolecular sieveCatalysisMordeniteCrystallographychemistry.chemical_compoundFerrieriteZeoliteSelectivityApplied Catalysis A: General
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