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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 16 (1977), S. 397-398 
    ISSN: 0031-9422
    Keywords: Pinaceae ; Pinus roxburghii ; hexacosylferulate ; structural determination.
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 23 (1984), S. 704-705 
    ISSN: 0031-9422
    Keywords: 5,3'',7''-trihydroxy-7,4',4-trimethoxy-(3',6'')-biflavone. ; Abies webbiana ; Pinaceae ; biflavonoids
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 33 (1950), S. 802-812 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Einwirkung von Lithiumaluminiumhydrid auf Corynanthein (I oder II) gelang es, zwei Reduktionsprodukte zu gewinnen: Desmethyl-corynanthein-alkohol(III) und Desmethoxy-corynantheinalkohol (VIIa oder VIIb), die durch Verseifung der Äthergruppe des Corynantheins und Reduktion der Estergruppe entstanden sind. Die Weiterreduktion des Desmethoxy-corynanthein-alkohols ergab den Dihydro-desoxy-corynanthein-alkohol (VIII). Durch vorsichtige Verseifung des Corynantheins mit einer Lösung von Chlorwasserstoff in Aceton und Äther wurde das Desmethyl-corynanthein (IV) erhalten, welches sich durch die braunrote Eisenchlorid-Reaktion und leichte Decarboxylierbarkeit zum Descarboxy-corynanthon (VI) als β-Ketosäure zu erkennen gibt. Descarboxy-corynanthon ist mit Yohimbon nicht identisch. Ob der Unterschied auf sterische Verschiedenheit von Corynanthein und Yohimbin zurückzuführen ist, oder ob Carboxyl- und Methylgruppe im Ring E des Corynantheins eine andere Lage als die Carboxyl- und OH-Gruppe im Yohimbin besitzen, muss weiter abgeklärt werden.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 277-280 
    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: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 117-124 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The notch sensitivity of high-density polyethylene (HDPE), polypropylene (PP), and polybutylene (PB) was evaluated using uniaxial tensile deformation and fractographic analysis. Each polyolefin was tested at relatively low and high molecular weights (MW). Only the lower MW HDPE was found to be clearly notch-sensitive. The lower MW PP exhibited some tendency toward notch sensitivity. The lower and higher MW PB, the higher MW HDPE, and the higher MW PP displayed notch strengthening. Whereas PB showed similar notched tensile performance regardless of molecular weight, both HDPE and PP showed higher susceptibility to notch sensitivity at lower molecular weights (and concomitant higher crystallinity). Tendencies toward notch sensitivity or notch stengthening were evidenced in the failure modes of these materials.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Structure of bis-indoline alkaloids of a novel typeThe structure of folicangine 4, a bis-indoline alkaloid from the leaves of Voacanga africana, is obtained by correlation with voafolidine 3a and isovoafolidine 3b. It requires an ether bridge between the two parts of the molecule, as in subsessiline (amataine 5a). Subsessiline-lactone, from the leaves of Voacanga thouarsii has structure 5b proved by correlation with 5a. The CD. curves of double-indole alkaloids of vobtusine type are given (Table 3).
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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