Search results for "Cyclic compound"

showing 10 items of 819 documents

Environmental analysis of chlorinated aromatic thioethers, sulphoxides and sulphones

1993

Abstract Chlorinated aromatic thioethers discussed here are polychlorinated dibenzothiophenes, thianthrenes and diphenylsulphides. Relatively little is known about their occurrence, behaviour and fate in the environment. Polychlorinated dibenzothiophenes and diphenylsulphides have recently been found to be formed in waste combustion and analysed in pulp mill effluents. Chlorinated sulphoxides and sulphones are usually metabolites or oxidation products of different chlorinated aromatic compounds. Different gas chromatographic-mass spectrometric techniques are used in the analysis of the chlorinated thioethers. The sulphoxides and sulphones, because of their higher polarity, can be isolated f…

chemistry.chemical_classificationChromatographyEnvironmental analysisOrganic ChemistrySulfoxideGeneral MedicineBiochemistryHigh-performance liquid chromatographyThin-layer chromatographyAnalytical ChemistrySulfonechemistry.chemical_compoundchemistrypolycyclic compoundsThiolOrganic chemistryGas chromatographyWaste combustionJournal of Chromatography A
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Determination of sterols, oxysterols, and fatty acids of phospholipids in cells and lipoproteins: A one-sample method

1998

In addition to fatty acids, especially polyunsaturated species, cholesterol oxidizes and leads to various oxygenated derivatives, named oxysterols. They display a wide range of adverse biological properties. Monitoring oxysterols is important in the evaluation of the potential risks associated with lipid oxidation. In the present study, a quick and reliable method was developed for analysis of oxysterols, sterols, and fatty acid composition of phospholipids in the same biological sample. Total lipid extraction was determined after addition of several internal standards (epicoprostanol for sterols, 19-hydroxy-cholesterol for oxysterol and di-heptadecanoyl-phosphatidylcholine for phospholipid…

chemistry.chemical_classificationChromatographyOxysterolCholesterolGeneral Chemical EngineeringOrganic ChemistryPhospholipidFatty acidSterolchemistry.chemical_compoundchemistryBiochemistryLipid oxidationpolycyclic compoundslipids (amino acids peptides and proteins)SaponificationPolyunsaturated fatty acidJournal of the American Oil Chemists' Society
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Gas chromatography of homologous esters

1985

Abstract The retention behaviour of C 1 C 18 n -alkyl esters of butanoic 2-, 3- and 4-chlorobutanoic acids was examined isothermally at several temperatures on SE-30 and OV-351 capillary columns. Retention increments showing the effects of each position of chlorine substitution are presented. The considerable enhancement of terminal chlorine substitution is discussed together with the corresponding behaviour of the monochloropropanoate esters.

chemistry.chemical_classificationChromatographyPrimary (chemistry)ChemistryCapillary actionOrganic Chemistrychemistry.chemical_elementGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundpolycyclic compoundsChlorineOrganic chemistryGas chromatographyMethyleneAlkylJournal of Chromatography A
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Über die Verbreitung von Flavonoiden bei pleurokarpen Laubmoosen II. Apigenin and Apigenin-7-rhamnoglucosid bei Pleurozium schreberi (Willd.) Mitt.

1980

Summary 12 species of pleurocarpous mosses have been investigated as to their content of flavonoids. Flavonoid tests on 11 species have given negative results. Only one species, Pleurozium schreberi , contains three flavonoids. They were purified by means of paper chromatography. Two of them are by chromatography, acid hydrolysis and absorption spectrum identical with apigenin and apigenin-7-rhamnoglucoside. The third flavonoid is as yet unidentified. Qualitative hydrolysis yields apigenin. The chemotaxonomic importance of the results is briefly discussed.

chemistry.chemical_classificationChromatographybiologyfungiFlavonoidfood and beveragesGeneral Medicinebiology.organism_classificationcarbohydrates (lipids)Paper chromatographyHydrolysischemistry.chemical_compoundchemistryApigeninheterocyclic compoundsAcid hydrolysisPleurozium schreberiZeitschrift für Pflanzenphysiologie
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Enzymatic and Chemo-Enzymatic Approaches Towards Natural and Non-Natural Alkaloids: Indoles, Isoquinolines, and Others

2010

Abstract The multi-step enzyme catalysed biosyntheses of monoterpenoid indole and isoquinoline alkaloids are described. Special emphasis is placed on those pathways leading to alkaloids of pharmacological and medicinal significance which have been fully elucidated at the enzyme level. The successful identification and cloning of cDNAs of single enzymes and their application provides great opportunities to develop novel strategies for both in vitro and in vivo alkaloid production in whole plants or tissue cultures, as well as in microbial systems such as Escherichia coli and yeast. Enzyme crystallisation, 3D analyses and site-directed mutation allowed rational engineering of enzyme substrate…

chemistry.chemical_classificationCloningIndole testendocrine systemorganic chemicalsAlkaloidSubstrate (chemistry)medicine.disease_causecomplex mixturesYeastchemistry.chemical_compoundEnzymechemistryBiochemistrymedicineheterocyclic compoundsIsoquinolineEscherichia coli
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Straightforward Stereoselective Access to Cyclic Peptidomimetics

2009

The preparation of cyclic dipeptide mimetics from chiral imino lactones derived from (R)-phenylglycinol is described. Key steps of the synthetic route included the fully stereoselective construction of a quaternary center, the formation of six-, seven-, or eight-membered lactams by means of an RCM cyclization, and the introduction of a new amino group within the lactam ring. The synthesis of a tripeptide mimetic is also reported.

chemistry.chemical_classificationCyclic compoundDipeptideChemistryStereochemistryMolecular MimicryOrganic ChemistryGlycineStereoisomerismDipeptidesTripeptideRing (chemistry)Peptides CyclicChemical synthesisCyclic peptideLactoneschemistry.chemical_compoundCyclizationEthanolaminesLactamLactone
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(S)-Mandelic acid enolate as a chiral benzoyl anion equivalent for the enantioselective synthesis of non-symmetrically substituted benzoins

2011

A strategy for the enantioselective synthesis of non-symmetrically substituted benzoins from (S)-mandelic acid and aromatic aldehydes has been developed. This strategy is based on a diastereoselective aldol reaction of the lithium enolate of the 1,3-dioxolan-4-one derived from (S)-mandelic acid and pivalaldehyde with aromatic aldehydes, which gives the corresponding aldols in good yields. Subsequent hydroxyl group protection as MEM ethers, basic hydrolysis of the dioxolanone ring, oxidative decarboxylation of the α-hydroxy acid moiety, and hydroxyl group deprotection provides chiral non-symmetrically substituted benzoins with high enantiomeric excesses.

chemistry.chemical_classificationDecarboxylationorganic chemicalsOrganic ChemistryEnantioselective synthesisMandelic acidBiochemistryAldehydechemistry.chemical_compoundAldol reactionchemistryDrug Discoverypolycyclic compoundsOrganic chemistryAldol condensationEnantiomeric excessOxidative decarboxylationTetrahedron
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A Specific Radioimmunoassay for the Determination of Low Quantities of Indole-3-acetic Acid in Spruce Needles of Healthy and Damaged Trees

1988

Summary The aim of the present investigation was to develop a radioimmunoassay for the quantification of indole-3-acetic acid in needles of Picea abies in damaged and phenotypically healthy trees. Phenols, lipophilic substances or compounds with cross-reactivity had to be separated from the extracts in several purification steps. Measurements were carried out between May and October 1986 on trees from two spruce plantations. Marked differences were found in IAA content in needles of healthy and damaged trees. In most cases the needles of the damaged trees contain lower endogenous IAA levels. The auxin levels also depended on the age of the tree, the year of needle formation, and the vegetat…

chemistry.chemical_classificationDevelopmental stagebiologyPhysiologyfood and beveragesPicea abiesRadioimmunoassayPlant Sciencebiology.organism_classificationWest germanychemistry.chemical_compoundSpecific radioimmunoassaychemistryAuxinBotanyheterocyclic compoundsPhenolsIndole-3-acetic acidAgronomy and Crop ScienceJournal of Plant Physiology
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ChemInform Abstract: Cycloaddition Reactions with Vinyl Heterocycles

2010

Publisher Summary The Diels-Alder reaction is one of the most common and elegant methods for the construction of six-membered rings. Although the number of Diels-Alder cycloadditions with open-chain and alicyclic dienes is very large, the number of examples with aromatic heterocyclic compounds is relatively small. The introduction of a vinyl group as a substituent onto a heterocycle increases the number of possible reactions. This new possibility, however attractive for synthetic purposes, is successful only with π-excessive five-membered heterocyclic derivatives with a few exceptions. The chapter discusses the reactions of vinyl heterocycles with carbodienophiles. The endocyclic and exo-en…

chemistry.chemical_classificationDimethyl acetylenedicarboxylateAlicyclic compoundchemistry.chemical_compoundchemistryPolymerizationDieneYield (chemistry)SubstituentOrganic chemistryGeneral MedicineSelectivityCycloadditionChemInform
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Reaktive Metabolite cancerogener polycyclischer Kohlenwasserstoffe: Synthese und Abfangreaktion von 9-Hydroxybenzo[a]pyren-4,5-oxid

1985

Le compose du titre est prepare a partir de l'acetate-9 de benzo [a] pyrene et piege par l'ethanethiol. Mecanismes

chemistry.chemical_classificationEthanethiolMetaboliteEpoxideGeneral MedicineMedicinal chemistrychemistry.chemical_compoundPolycyclic compoundchemistrypolycyclic compoundsOrthoesterPhenolsCarcinogenBond cleavageAngewandte Chemie
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