Search results for "Organic Chemicals"

showing 8 items of 728 documents

New simple hydrophobic proline derivatives as highly active and stereoselective catalysts for the direct asymmetric aldol reaction in aqueous medium

2008

New 4-substituted acyloxyproline derivatives with different hydrophobic properties of the acyl group were easily synthesized and used as catalysts in the direct asymmetric aldol reaction between cyclic ketones (cyclohexanone and cyclopentanone) and several substituted benzaldehydes. Reactions were carried out using water, this being the best reaction medium examined. Screening of these catalysts showed that compounds bearing the most hydrophobic acyl chains [4-phenylbutanoate and 4-(pyren-1-yl)butanoate] provided better results. The latter catalysts were successfully used in only 2 mol% at room temperature without additives to give aldol products in excellent stereoselectivities. These resu…

or-ganic catalysiorganic chemicalsOrganic ChemistryketoneSubstituentCyclohexanoneSettore CHIM/06 - Chimica OrganicaCyclopentanoneCatalysisaldehydeCatalysischemistry.chemical_compoundchemistryAldol reactionMoietyOrganic chemistryaldol reactionStereoselectivityprolineAcyl group
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Covalent Protein Binding of Vinyl Chloride Metabolites During Co-Incubation of Freshly Isolated Hepatocytes and Hepatic Sinusoidal Cells of Rats

1983

Proteins of isolated rat hepatic sinusoidal cells incubated with 14C-vinyl chloride, rat liver microsomes and an NADPH-regenerating system were alkylated by vinyl chloride metabolites formed by microsomes. This suggests that reactive vinyl chloride metabolites can penetrate sinusoidal cells. Protein alkylation in isolated hepatic sinusoidal cells was higher when these were co-incubated with isolated hepatocytes, indicating that reactive vinyl chloride metabolites formed by hepatocytes are stable enough to diffuse out of hepatocytes into sinusoidal cells. Glutathione added to the incubation medium inhibited the covalent protein binding of vinyl chloride metabolites in sinusoidal cells as wel…

organic chemicalsCelltechnology industry and agricultureGlutathioneChlorideVinyl chloridechemistry.chemical_compoundmedicine.anatomical_structurechemistryBiochemistryIn vivoCovalent bondmedicineMicrosomeProtein alkylationmedicine.drug
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Synthesis, Structure and Solvatochromism of the Emission of Cyano-Substituted Oligo(phenylenevinylene)s

2001

Strongly luminescent and highly soluble oligo(phenylenevinylene)s with five benzene rings and cyano groups in different positions of the terminal styrene units were prepared by means of Horner and Knoevenagel reactions. The substitution pattern − cyanide moieties on the vinyl or on the aromatic regions, together with the effect of auxochromic groups − has distinct influences on the electronic spectra, particularly on the fluorescence. Polar solvents induce red shifts and strongly reduce the fluorescence intensity of the vinyl-substituted oligomers. Cyano substitution increases the electron affinity of the oligomers; this effect is more pronounced for molecules with vinyl cyanides and can be…

organic chemicalsOrganic ChemistrySolvatochromismPhotochemistryOligomerStyrenechemistry.chemical_compoundBenzonitrilechemistryElectron affinity (data page)Polymer chemistryMoleculeKnoevenagel condensationPhysical and Theoretical ChemistryBenzeneEuropean Journal of Organic Chemistry
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Fluorine-containing functionalized cyclopentene scaffolds through ring contraction and deoxofluorination of various substituted cyclohexenes

2018

The fluorination of some highly‐functionalized cyclopentene derivatives, obtained from various substituted cyclohexenes through a ring‐opening/ring‐contraction procedure, has been investigated. The transformations were found to be highly substrate dependent, and led to the formation of various functionalized alicyclic compounds or heterocycles containing allyl difluoride or vinyl fluoride moieties. peerReviewed

organic chemicalsaldol reactionaminohapotstereoselectivityring contractionorgaaniset yhdisteetfluoriditfluori
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Design, Synthesis and Evaluation of Fluorescent Analogues of Abscisic Acid

2020

A fluorescent analogue of abscisic acid has been prepared by combining (S)‐abscisic acid (ABA) with nitrobenzoxadiazole (NBD) fluorophore using ethanol amine as a linker. Isomerization of the double bond at the side chain of abscisic acid happened during the synthesis. The resulting fluorophore analogues derived from both isomeric compounds entered cells suggesting a wide applicability of the ABA‐NBD conjugates as fluorescent probes to study ABA mechanism of action. The functional properties of the isomeric ABA‐NBD conjugates were tested in vitro, by measuring TNFα expression and nitrite concentration in LPS‐stimulated macrophages and compared with their non‐fluorescent ABA isomers. Rationa…

organic chemicalsfungifood and beveragesGeneral Chemistryfluorescent analoguesFluorescenceabscisic acidchemistry.chemical_compoundchemical probesDesign synthesischemistryBiochemistryinflammationneurodegenerative disorderslipids (amino acids peptides and proteins)Abscisic acidChemistrySelect
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Estudio DS 103-282: Relajante Muscular en Lumbalgia Aguda o Lumbago : (estudio doble ciego de Tizanidina + Paracetamol V s Placebo + Paracetamol)

1989

The clinic efficiency and tolerance of tizanidina + paracetamol was compared with placebo+ paracetamol in an estadistical study and in with were treated 50 patients diagnosed of acote back pain or lumbago. Dif'ferent clinical parámeters was dimished in the group ofthe group of tizanidina + paracetamol.

organic chemicalshealth services administrationUNESCO::CIENCIAS MÉDICASdigestive oral and skin physiology:CIENCIAS MÉDICAS [UNESCO]human activities
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UV filters: From sunscreens to human body and the environment

2007

Recognition of the harmful effects of ultraviolet (UV) radiation on the skin has triggered development of organic chemicals (commonly referred as UV filters) that can absorb UV radiation and attenuate the negative effects of sunlight exposure. Depending on the properties and the intended degree of protection, a wide array of combinations is being marketed as delivering protection against most kinds of UV-induced skin damage. However, some UV filters have dermatological implications, so maximum applicable concentrations have been established. To monitor to what extent commercial products comply with the mandatory limits, several analytical methods have been used for their determination in co…

p-aminobenzoic acidvivo skin penetrationpercutaneous-absorptiongas chromatographymedia_common.quotation_subjectmedicine.disease_causeCosmeticsAnalytical ChemistryMatrix (chemical analysis)by-productSkin surfaceliquid-chromatographyWater environmentmedicineliquid chromatographytopical applicationSpectroscopyVolume concentrationmedia_commonsunscreensun protection factorChromatographyOrganic chemicalsChemistryoctyl-methoxycinnamatepercutaneous absorptionin-vitro permeationsolid-phase microextractionSkin penetrationBiochemical engineeringuv filterenvironmentmetabolismUltravioletchromatography-mass-spectrometryTrAC Trends in Analytical Chemistry
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Carotenoids under the spotlight: from diet to the retina

2016

Revue; Carotenoids under the spotlight: from diet to the retina. 12. congress of the international society for the study of fatty acids and lipids

retinalutein[SDV.MHEP] Life Sciences [q-bio]/Human health and pathology[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionorganic chemicalseducationfood and beverages[SDV.AEN] Life Sciences [q-bio]/Food and Nutritionprevention[SDV.MHEP.OS] Life Sciences [q-bio]/Human health and pathology/Sensory Organs[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathology[ SDV.MHEP.OS ] Life Sciences [q-bio]/Human health and pathology/Sensory Organssense organs[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organsdiet[SDV.AEN]Life Sciences [q-bio]/Food and Nutritionhealth care economics and organizations[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
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