Search results for "EOs"

showing 10 items of 2714 documents

ChemInform Abstract: o-(Hydroxyalkyl)phenyl P-Chirogenic Phosphines as Functional Chiral Lewis Bases.

2013

The stereoselective synthesis of P-chirogenic phosphines bearing an o-hydroxyalkyl chain is described.

Chain (algebraic topology)ChemistryStereochemistryStereoselectivityGeneral MedicineLewis acids and basesChemInform
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High accuracy [sup 18]O(p,α)[sup 15]N reaction rate in the 8⋅10[sup 6]–5⋅10[sup 9] K temperature range

2011

The 18O(p,α)15N reaction is of great importance in several astrophysical scenarios, as it influences the production of key isotopes such as 19F, 18O and 15N. In this work, a high accuracy 18O(p,α)15N reaction rate is proposed, based on the simultaneous fit of direct measurements and of the results of a new Trojan Horse experiment. In particular, we have focused on the study of the broad 660 keV 1/2+ resonance. Since Γ∼100–300 keV, it strongly influences the nearly‐zero‐energy region of the cross section by means of the low‐energy tail of the resonant contribution and dominates the cross section at higher energies. Here we provide a factor of 2 larger reaction rate above T∼0.5 109 K based ov…

Chemical kineticsNuclear reactionReaction rateNuclear physicsCross section (physics)NucleosynthesisChemistryResonanceAlpha particleAtomic physicsCharged particleAIP Conference Proceedings
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Stereoselective syntheses of piperidinones and their modification by organometallic coupling reactions

2007

Dehydropiperidinones stereoselectively obtained from N-arabinosyl imines were iodinated at the enaminone structure. Knochel iodine-magnesium exchange afforded Grignard compounds of these piperidinone derivatives which reacted, either directly or after transmetalation to zinc or copper intermediates, with alkyl-, aryl- or acylhalides to give correspondingly substituted piperidinones. Stereoselective conjugate allyl cuprate addition to a thus obtained 5-allyl dehydropiperidinone and ring-closing metathesis of the product gave a hydroquinolinone containing three stereogenic centers.

Chemistry OrganicMolecular ConformationStereoisomerismCrystallography X-RayMetathesisBiochemistryCoupling reactionStereocenterchemistry.chemical_compoundTransmetalationOrganometallic CompoundsOrganic chemistryMagnesiumPhysical and Theoretical ChemistryPiperidonesGroup 2 organometallic chemistryMolecular StructureChemistryArylOrganic ChemistryStereoisomerismZincModels ChemicalStereoselectivityIminesCopperIodineOrg. Biomol. Chem.
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Interlamellar Reactions of Tetracalcium Aluminate Hydrates with Water and Organic Compounds

1967

Tetracalcium aluminate hydrates are the first example of layer-structured crystals containing neutral sheets, which are highly capable of interlamellar adsorption of water and neutral organic compounds. In this respect tetracalcium aluminate hydrates present new aspects of the phenomenon of swelling, and bring about the challenge of comparison with the frequently examined clay-organic compounds. This report is concerned with the probable monolayer structure of tetracalcium aluminate hydrate which forms five hydration stages. A summary concerning configuration and properties of adsorption complexes with approximately 500 selected organic substances follows. As far as these substances are hom…

ChemistryAluminateInorganic chemistrySoil Sciencechemistry.chemical_compoundAdsorptionGeochemistry and PetrologyMonolayerEarth and Planetary Sciences (miscellaneous)medicineSwellingmedicine.symptomBiogeosciencesClay mineralsHydrateWater Science and TechnologyClays and Clay Minerals
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Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water

2009

Several polystyrene-supported proline dipeptides and a prolinamide derivative were prepared by thiol–ene coupling. These materials were used as catalysts for the direct asymmetric aldol reaction in water, and results compared with unsupported catalysts in water. Such an approach gave more active or stereoselective catalysts compared to the unsupported compounds, showing that our immobilization procedure may be useful to develop catalytic materials with enhanced performance. Moreover, these catalysts can be recovered and reused for at least nine times without loss of activity or can be easily regenerated when their activity has decreased. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, …

ChemistryCatalyst supportOrganic ChemistryEnantioselective synthesisSettore CHIM/06 - Chimica OrganicaChemical synthesisCatalysisAldol reactionOrganocatalysisOrganic chemistryDipeptide Organocatalysis Prolinamide Proline Supported catalystAldol condensationStereoselectivityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Brain choline has a typical precursor profile.

1998

Choline is product and precursor to both acetylcholine and membrane phospholipids, and, in the brain, is ultimately provided by the circulation. The brain is protected from excess choline and choline deprivation by a refined system of homeostatic mechanisms that maintain a level of extracellular choline that, for its role as precursor, meets saturation criteria under normal conditions. The kinetic and activity profiles of choline are typical for a biosynthetic precursor.

ChemistryGeneral NeuroscienceBrainCholine acetyltransferaseAcetylcholineCholinechemistry.chemical_compoundKineticsMembraneBiochemistryPhysiology (medical)SynapsesmedicineExtracellularCholinergicCholineAnimalsHomeostasisHumansCholinergic mechanismsAcetylcholineHomeostasisPhospholipidsmedicine.drugJournal of physiology, Paris
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RAB18 impacts autophagy via lipid droplet-derived lipid transfer and is rescued by ATG9A

2018

AbstractAutophagy is a lysosomal degradation pathway that mediates protein and organelle turnover and maintains cellular homeostasis. Autophagosomes transport cargo to lysosomes and their formation is dependent on an appropriate lipid supply. Here, we show that the knockout of the RAB GTPase RAB18 interferes with lipid droplet (LD) metabolism, resulting in an impaired fatty acid mobilization. The reduced LD-derived lipid availability influences autophagy and provokes adaptive modifications of the autophagy network, which include increased ATG2B expression and ATG12-ATG5 conjugate formation as well as enhanced ATG2B and ATG9A phosphorylation. Phosphorylation of ATG9A directs this transmembra…

ChemistryLipid dropletAutophagyOrganellePhosphorylationCellular homeostasisGTPaseRabRAB18Cell biology
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Dendrobium officinale Polysaccharide Alleviates Intestinal Inflammation by Promoting Small Extracellular Vesicle Packaging of miR-433-3p

2021

Dendrobium officinale polysaccharide (DOP) attenuates inflammatory bowel disease (IBD), but its role in regulating cross-talk between intestinal epithelial cells (IEC) and macrophages against IBD is unclear. This study aimed to investigate DOP protective effects on the intestinal inflammatory response through regulation by miRNA in small extracellular vesicles (sEVs). Our results show that DOP interfered with the secretion of small extracellular vesicles (DIEs) by IEC, which reduced the levels of inflammatory mediators. Increased miR-433-3p expression in DIEs was identified as an important protector against intestinal inflammation. DOP regulated the loading of miR-433-3p by hnRNPA2B1 into t…

ChemistryMAPK8General ChemistryExtracellular vesiclemedicine.diseaseInflammatory bowel diseaseCell biologyProinflammatory cytokinemicroRNAmedicineMacrophageSecretionGeneral Agricultural and Biological SciencesHomeostasisJournal of Agricultural and Food Chemistry
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Stereoselective Synthesis of Bromopiperidinones and their Conversion to Annulated Heterocycles

2009

N-Galactopyranosyl- and N-glucopyranosyl imines of aliphatic, aromatic and heteroaromatic aldehydes react with 1-methoxy-3-trimethylsilyloxy-1,3-butadiene in a domino Mannich-Michael reaction cascade to give 2-substituted 5,6-dehydro-piperidin-4-ones with high diastereoselectivity. Treatment of these cyclic enaminones with N-bromo-succinimide yields the corresponding 2-substituted 5-bromo-5,6-dehydropiperidinones which react with L-SelectrideⓇ or methylcuprate to afford the saturated bromo-piperidinones with high diastereoselectivity. Condensation reactions of these products with thioamides afford thiazolopiperidines

ChemistryOrganic chemistryStereoselectivityGeneral ChemistryCondensation reactionDominoZeitschrift für Naturforschung B
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Enantioselective Synthesis of P-Chirogenic Phosphorus Compounds via the Ephedrine-Borane Complex Methodology

2008

The stereoselective synthesis of P-chirogenic organophosphorus compounds using the versatile ephedrine-methodology is reported. The principle of the method is based on the diastereoselective preparation of 1,3,2-oxazaphospholidine borane 3 from ephedrine 2 and regio- and stereoselective ring-opening of the heterocycle leading to an aminophosphine borane 4. Finally, these ring-opening products 4 are easily transformed into P-chirogenic organophosphorus compounds, by subsequent highly stereoselective reactions involving electrophilic or nucleophilic strategies.

ChemistryPhosphorusOrganic ChemistryEnantioselective synthesischemistry.chemical_elementBoraneBiochemistryInorganic Chemistrychemistry.chemical_compoundNucleophileElectrophilemedicineOrganic chemistryStereoselectivityEphedrinemedicine.drugPhosphorus, Sulfur, and Silicon and the Related Elements
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