Search results for "Paper chromatography"

showing 7 items of 17 documents

Über die Verbreitung von Flavonoiden bei pleurokarpen Laubmoosen I. Apigenin-7-rhamnoglucosid bei Hylocomium splendens (Hedw.) Br. eur.

1977

Summary 15 species of pleurocarpous mosses have been investigated as to their content of flavonoids. Flavonoid tests on 14 species have given negative results. Only one species, Hylocomium splendens , contains one flavonoid. It was purified by means of paper chromatography and is by chromatography and absorption spectrum identical with rhoifolin (apigenin-7-neohesperidoside). Partial acid hydrolysis yields apigenin-7-monoglucoside and rhamnose, quantitative hydrolysis apigenin, rhamnose and glucose. They were identified by comparison with authentic samples.

chemistry.chemical_classificationChromatographybiologyRhamnoseFlavonoidfood and beveragesGeneral Medicinebiology.organism_classificationPartial acid hydrolysischemistry.chemical_compoundPaper chromatographyHydrolysischemistryRhoifolinApigeninHylocomium splendensZeitschrift für Pflanzenphysiologie
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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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Isolierung und Charakterisierung eines Dihydroflavonols bei dem Laubmoos Georgia pellucida (L.) Rabh

1977

Summary By means of paper chromatography a dihydroflavonol was isolated from the methanolic extract of the moss Georgia pellucida and partially characterized. It has the chromatographic and spectral characteristics of a 5-deoxydihydroflavonol glycoside with B-ring orthodihydroxyl group.

chemistry.chemical_classificationPaper chromatographyChromatographychemistryPellucidabiologyBotanyGlycosideGeneral Medicinebiology.organism_classificationZeitschrift für Pflanzenphysiologie
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Die Flavonoide von Riccia fluitans L.

1978

Summary Five flavonoids of Riccia fluitans were analysed by means of paper chromatography and uv-spectral data. One substance was identified as luteolin, the others are glycosides of apigenin and luteolin: apigenin-7-O-glucuronide, luteolin-7-O-glucuronide, luteolin-7-O-glucuronide-3’-O-rhamnoside and luteolin-6,8-di-C-glycoside (lucenin).

chemistry.chemical_classificationchemistry.chemical_compoundPaper chromatographybiologychemistryApigeninBotanyGlycosideGeneral MedicineRiccia fluitansbiology.organism_classificationLuteolinZeitschrift für Pflanzenphysiologie
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On the Occurrence of Flavonoids in the acrocarpous Mosses

1978

Summary By means of paper chromatography two flavonoids were isolated from the methanolic extract of the moss Mnium undulatum. One substance was identified by chromatographic data, absorption spectra and acid hydrolysis as isovitexin-7-0-glucoside (saponarin). The second substance resists acid hydrolysis and is by chromatography and absorption spectrum identical with apigenin-6,8-di-C-glycoside (viccnin).

chemistry.chemical_compoundPaper chromatographyChromatographyAbsorption spectroscopychemistrySaponarinIsovitexinAcid hydrolysisGeneral MedicineZeitschrift für Pflanzenphysiologie
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Eine blockierungsmethode zur darstellung molekular-einheitlicher hydroxyphenylenmethylen-verbindungen

1973

Hydroxyphenylenmethylen-Verbindungen wurden nach verschiedenen Verfahren dargestellt. Dabei wurden folgende Ausgangsprodukte verwendet: p-Kresol und Formaldehyd (Gl. (i)) oder p-Kresol und 2,6-Bis(hydroxymethyl)-p-kresol (4) (Gl. (ii)), (Duplikations-Verfahren), 2-Chlor-6-(3′-chlormethyl-2-hydroxy-5′-methylbenzyl)-p-kresol (5) und 2-Chlor-p-kresol (Gl. (iii)), (schrittweise Synthese) oder 2-Chlor-6-chlormethyl-p-kresol (8) und p-Kresol (Gl. (iv)) (Blockierungsmethode). Die nach den verschiedenen Methoden entstandenen Reaktionsprodukte wurden papierchromatographisch aufgetrennt und identifiziert unter Berucksichtigung der bei der Analyse auftretenden Nebenreaktionen. Hydroxyphenylene methyle…

chemistry.chemical_compoundPaper chromatographychemistryPolymer chemistryFormaldehydeHydroxymethylMethyleneDie Makromolekulare Chemie
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Papierchromatographische und papierionophoretische Untersuchungen zur Freilegung und Trennung der Hypophysen-Hinterlappen-Hormone Oxytocin und Vasopr…

1956

medicine.medical_specialtyPaper chromatographyEndocrinologyOxytocinChemistryInternal medicineDrug DiscoverymedicinePharmaceutical Sciencemedicine.drugArchiv der Pharmazie
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