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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1979 (1979), S. 1116-1121 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Constituents of Euphorbiaceae, Vl. - Three New 4-Deoxyphorbol Triesters from Euphorbia biglandulosa Desf.The new 4-deoxyphorbol triesters 13,20-O-diacetyl-12-O-(Z,E)-2,4-octadienoyl-4-deoxyphorbol (1), 20- O-acetyl-12-O-(Z,E)2,4-octadienoyl-13-O-propionyl-4-deoxyphorbol (2) and 20-O-acetyl-13-O-isobutyryl-12-O-(Z,E)-2,4-octadienoyl-4-deoxyphorbol (3) were isolated from the lipophilic phase of the latex sap of Euphorbia biglandulosa Desf. Their structure and that of the compounds 1a, 1b,2a and 3a formed on hydrolysis have been established by IR-, 1H-NMR- and mass spectroscopy. - The natural compounds have an irritating action on the skin of mice, a toxic on fishes and inhibit the oxidative phosphorylation of isolated heart mitochondria.
    Notes: Aus der lipophilen Phase des Milchsaftes von Euphorbia biglandulosa Desf. wurden 13,20-O-Diacetyl-12-O-(Z,E)-2,4-octadienoyl-4-desoxyphorbol (1), 20-O-Acetyl-12-O-(Z,E)-2,4-octa-dienoyl-13-O-propionyl-4-desoxyphorbol (2) und 20-O-Acetyl-13-O-isobutyryl-12-O-(Z,E)-2,4-octadienoyl-4-desoxyphorbol (3) isoliert. Die Strukturen dieser Verbindungen und ihrer Hydrolysederivate 1a, 1b, 2a,3a wurden durch IR-, 1H-NMR- und Massen-Spektroskopie belegt. -Die Substanzen 1-3 wirken als Fischgifte; sie sind hautätzend und hemmen die oxidative Phosphorylierung isolierter Herzmitochondrien.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1979 (1979), S. 751-756 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Simple Synthesis of Substituted 5,6-Dihydro-2H-pyran-2-ones under Mild ConditionsThe synthesis of 3,5,5-trisubstituted 5,6-dihydro-2H-pyran-2-ones 5 via Knoevenagel reaction in the presence of TiCl4/pyridine in THF is described.
    Notes: 3,5,5-Trisubstituierte 5,6-Dihydro-2H-Pyran-2-one 5 wurden durch Knoevenagel-Reaktion in THF in Gegenwart von TiCl4/Pyridin synthetisiert.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1981 (1981), S. 565-568 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Facile Synthesis of Substituted 5,6-Dihydro-2H-pyran-2-ones under Mild ConditionsThe synthesis of the 3,5,5-trisubstituted 5,6-dihydro-2H-pyran-2-ones 3a-k via Knoevenagel reaction in the presence of TiCl4/pyridine in THF is described.
    Notes: Die 3,5,5-trisubstituierten 5,6-Dihydro-2H-pyran-2-one 3a-k wurden durch Knoevenagel-Reaktion in THF in Gegenwart von TiCl4/Pyridin synthetisiert.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1979 (1979), S. 2028-2035 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Constituents of Boraginaceae.  -  Triterpene Saponins from Anchusa officinalis L.The structure of three saponins of Anchusa officinalis L. has been elucidated as 3-O-β-D-glucopyranosyloleanolic acid α-D-glucopyranosyl ester (5), 3-O-[2,3-di-O-(β-D-glucopyranosyl)-β-D-glucopyranosyl]oleanolic acid (7) and 3-[3-O-(β-D-glucopyranosyl)-β-D-glucopyranosyl]-oleanolic acid α-D-glucopyranosyl ester (9) by use of IR, 1H-NMR and MS measurements (Tables 1 and 2).
    Notes: Aus dem ethanolischen Extrakt von Anchusa officinalis L. wurden drei neue Saponine, die Anchusoside 1, 2 und 7 isoliert. Die Verbindungen konnten durch IR-, 1H-NMR- und Massenspektroskopie sowie Hydrolysen als 3-O-β-D-Glucopyranosyloleanolsäure-α-D-glucopyranosylester (5), 3-O-[2,3-Di-O-(β-D-glucopyranosyl)-β-D-glucopyranosyl]oleanolsäure (7) und 3-[3-O-(β-D-Glucopyranosyl)-β-D-glucopyranosyl]oleanolsäure-α-D-glucopyranosylester (9) identifiziert werden (Daten in den Tabellen 1 und 2).
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Constituents of Euphorbiaceae, IV1).  -  Constitution of the Isomeric O-(ß-Hydroxy-γ-hydroxycarbonyl-ß-methylbutanoyl)shikimic Acids from Euphorbia biglandulosa Desf.The composition and structure of the isomeric O-(ß-hydroxy-γ-hydroxycarbonyl-ß-methylbutanoyl)shikimic acids 7 and 8 isolated from Euphorbia biglandulosa have been determined (74% 5-O-, 26% 3-O-derivative) by comparative 1H-NMR spectroscopy of the shikimic acid derivatives methyl 3,4,5-tri-O-acetylshikimate (3), methyl 3,4-O-(phenylboranediyl)shikimate (4), and methyl 5-O-acetylshikimate (6). The conformation of the shikimic acid derivatives is discussed.
    Notes: Durch vergleichende Analyse der 1H-NMR-Spektren der Shikimisäurederivate 3,4,5-Tri-O-acetylshikimisäure-methylester (3), 3,4-O-(Phenylborandiyl)shikimisäure-methylester (4) und 5-O-Acetylshikimisäure-methylester (6) wurden die Zusammensetzung des Isomerengemisches und die Konstitution der aus Euphorbia biglandulosa gewonnenen O-(β-Hydroxy-γ-hydroxycarbonyl-β-methylbutanoyl)shikimisäuren 7 und 8 aufgeklärt (74% 5-O-, 26% 3-O-Derivat). Die Konformation der Shikimisäurederivate wird diskutiert.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Constituents of Euphorbiaceae, III.  -  Calcium Salts of Isomeric O-(β-Hydroxy-β-methyl-glutaroyl)shikimic Acids from Euphorbia biglandulosa Desf.A mixture of the calcium salts of two isomeric O-(β-hydroxy-β-methylglutaroyl)shikimic acids 1 was isolated from the aqueous phase of the coagulated latex sap of E. biglandulosa. The free acids 1 and their hydrolysis products, shikimic acid (2) and β-hydroxy-β-methylglutaric acid (3), have been identified by IR, 1H-NMR, and mass spectrometry.
    Notes: Aus der wäßrigen Phase des koagulierten Milchsaftes von E. biglandulosa wurde das Gemisch der Calciumsalze von zwei isomeren O-(β-Hydroxy-β-methylglutaroyl)shikimisäuren 1 isoliert. Die freien isomeren Säuren 1 sowie deren Hydrolyseprodukte Shikimisäure (2) und β-Hydroxy-β-methylglutarsäure (3) konnten durch IR-, 1H-NMR- und Massenspektroskopie identifiziert werden.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 752 (1971), S. 175-181 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: D-Xylose Esters of p-Coumaric AcidWe have synthesized the 1-O-, 2-O- and 3-O-p-coumaroyl-D-xylopyranoses 1-7; the esters are investigated by NMR-spectroscopy, thin-layer- and paper chromatography.
    Notes: Es werden die 1-O-, 2-O- und 3-O-p-Cumaroyl-D-xylopyranosen 1-7 synthetisiert und NMR-spektroskopisch sowie dünnschicht- und papierchromatographisch untersucht.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Constituents of Euphorbiaceae.II-The Calcium Salt of the 5,5-Dimethyl-5,6-dihydro-u- pyrone-3,4-dicarboxylic Acid from Euphorbia biglandulosa Desf. an Inhibitor of Cell RespirationThe calcium salt 2 of 5,5-dimethyl-5,6-dihydro-a-pyrone-3,4-dicarboxylic acid was isolated from the aqueous phase of the coagulated latex sap of E. biglandulosa. The structures of the free acid 3, its dimethyl ester 4, and its dihydro compound 5 have been established by IR-, 1H-NMR-, and mass spectroscopy. 2 and 3 inhibit the oxidative phosphorylation of heart and liver mitochondria').
    Notes: Aus der wäßrigen Phase des koagulierten Milchsaftes von E. biglandulosa wurde das Calciumsalz 2 der 5,5-Dimethyl-5,6-dihydro-a-pyron-3,4-dicarbonsäure isoliert. Die Strukturen der freien Saure 3, des daraus erhaltenen Dimethylesters 4 sowie der Dihydroverbindung 5 konnten durch IR-, 1H-NMR- und Massenspektroskopie ermittelt werden. 2 und 3 hemmen die oxidative Phosphorylierung an Herz- und Lebermitochondrien.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1982 (1982), S. 191-195 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Substituted 5,6-Dihydro-2H-pyran-2-ones and their Reaction with BromineThe synthesis of the substituted 5,6-dihydro-2H-pyran-2-ones 2a-f and the reaction of 2a-e and 1g with bromine to 3a-f are described.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1983 (1983), S. 1448-1450 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Constituents of Cupuliferae, 6. - A Novel Triterpene Saponin from Quercus ilex L.From leaves of Quercus ilex L. a new triterpene saponin has been isolated and identified as the α-D-glucopyranosyl ester 3 of the 2α,3β,19α,23-tetrahydroxy-12-ursen-28-oic acid (1).
    Type of Medium: Electronic Resource
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