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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 224 (1935), S. 194-212 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 17 (1971), S. 1499-1501 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 83 (1971), S. 766-766 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 55 (1972), S. 2277-2286 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two new syntheses of spiro[4.4]nonane-1, 6-dione (I) are described: one by rearrangement of 1,6-epoxy-bicyclo[4.3.0]-nonane-2-one (IV) with boron trifluoride, the other by an acid catalyzed, intramolecular Claisen condensation of 4-(2-oxocyclopentyl)-butyric acid. Spiro[4.4]-nonane-1,6-dione is converted into trans, trans-spiro[4.4]nonane-1,6-diol which is resolved into enantiomers via the diastereomeric esters with (-)-camphanic acid. (+)-(5S)-Spiro[4.4]nona-1,6-diene (III) is prepared from (1R, 6R)-trans,trans-spiro[4.4]nonane-1,6-diol (II) by pyrolysis of the corresponding bis-4-methylphenyl-thionocarbonate. This modification of the Chugaev reaction is particularly useful with sterically hindered alcohols which cannot be converted into S-me-thylxanthates. The circular dichroism, UV.- and NMR.-spectrum of optically active spiro[4.4]-nonane-1,6-diene are discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 139 (1970), S. 83-102 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The interaction of Na-DNS and actinomine in diluted aqueous NaCl solutions is investigated by means of small angle X-ray scattering. Ultrasonic degradation of high molecular DNS yielded particles of suitable length so that besides the cross section also the particle length could be determined. DNS solutions saturated with actinomine have been measured down to a DNS concentration of 0,045 g/100 ml. We observed an extension of the DNS fragments after interacting with actinomine by 18%. The amount of actinomine in the addition compound has been determined: As an average, 7.1 base pairs are combined with one actinomine molecule. Also a shell of counter and by ions surrounding the DNS particles has been found and its dimensions have been determined. From the pseudo cross section scattering curves the inner parts of the cross section scattering curves valid for infinitely long particles could be reconstructed as calculations proceeded.
    Notes: Es wird die Wechselwirkung von Na-DNS und Actinomin in verdünnten, wäßrigen NaCl-Lösungen mit den Methoden der Röntgenkleinwinkelstreuung untersucht. Dafür mußten aus hochmolekularer DNS durch Ultraschallabbau Teilchen geeigneter Länge hergestellt werden, so daß neben dem Querschnitt auch die Teilchenlänge mit der Röntgenkleinwinkelstreuung noch zu erfassen war. Die Messungen erfolgten an mit Actinomin gesätigten DNS-Lösungen bis herab zu einer DNS-Konzentration von 0,045 g/100 ml. Es konnte dabei eine Streckung der abgebauten DNS-Partikel bei Anlagerung von Actinomin um 18% festgestellt und die Menge des an die DNS gebundenen Actinomins bestimmt werden: im Mittel wird auf 7,1 Basenpaare ein Actinomin-Molekül angelagert. Gleichzeitig wurde eine die DNS-Partikel umgebende Hülle aus Gegen- und Bei-Ionen durch Beugung festgestellt und deren räumliche Dimension ermittelt. Im Verlauf der Auswertung ist es auch gelungen, aus den vorliegenden Pseudo-Querschnittsstreukurven die für unendlich lange Teilchen gültigen Querschnittsstreukurven-Innenteile zu rekonstruieren.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 10 (1971), S. 727-728 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 68 (1935), S. 989-991 
    ISSN: 0365-9631
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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