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  • 1
    Electronic Resource
    Electronic Resource
    Die Reduktion von α-Aminocarbonsäureestern zu Aminoalkoholen mittels Lithiumaluminiumhydrid (1948)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 31 (1948), S. 1617-1623 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Reduktion mit Lithiumaluminiumhydrid wurde aus den entsprechenden Estern von α-Aminocarbonsäuren die folgenden Aminoalkohole dargestellt: D, L-Phenylalaninol, L(-)-Phenylalaninol, L(-)-Tyrosinol, L(+)-Alaninol, L(+)-Leucinol, L,(+)-2-Oxymethylpyrrolidin (L(+)-Prolinol), L(+)-2-Aminobutandiol-(1,4) (L(+)-Asparaginol), D, L-2-Aminobutandiol-(1,4) (D, L-Asparaginol) und 2-Amino-propandiol-( 1,3).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19480310624
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    L-Valinol und L-Tyrosinol (1949)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 32 (1949), S. 1156-1157 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Reduktion mit Lithiumaluminiumhydrid wurden aus L-Valin-methylester L-Valinol und aus L-Tyrosin-methylester L-Tyrosinol in guten Ausbeuten hergestellt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19490320374
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    L-Histidinol (1949)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 32 (1949), S. 1936-1938 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Reduktion von Dibenzoyl-L-histidinmethylester mit LiAlH4 wurden Monobenzoyl-L-histidinol und aus letzterem durch Verseifung L-Histidinol hergestellt. Letztere Verbindung zeigt ähnliche pharmakologische Wirkung wie Histamin, aber erst in 1000-3000 mal höherer Dosis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19490320619
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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