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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 222-229 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogenated pyridines IV. Nuclear chlorinated pyridine-3-carboxylic acids.Chlorinated pyridine-3-carboxylic acids (nicotinic acids) are readily accessible by oxidation of nuclear chlorinated 3-chloromethyl-pyridines. The catalytic oxidation procedures proved to be by far the best ones of the methods tested.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 229-235 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogenated pyridines V.Fluorinated and brominated pyridine compounds.Ring chlorinated 3-chloromethyl-pyridines provide a source of new halogenopyridines the fluorination of which is described. Variously substituted 2, 6-dibromopyridines are prepared from the corresponding dichloro compounds by halogen displacement with hydrogen bromide in acetic acid at elevated temperatures.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 211-221 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogenated pyridines III. Di- and trihalogenated pyridine-3-aldehydes.Three methods for the preparation of new ring chlorinated pyridine-3-aldehydes are investigated. Reactions of the new aldehydes are reported.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 190-211 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogenated pyridines II. Reactions of 3-halogenomethyl-pyridines.The facile syntheis of 3-halogenomethyl-pyridines provides an easy access to a variety of new 2, 6-di- and 2, 5, 6-trihalogented pyridines with various functional groups in the 3-position of the pyridine ring. Substitution reactions of the 3-halogenomethyl groups, their Friedel Crafts reactions, and nitrations of the halogenated pyridine ring are reported.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 60 (1977), S. 907-921 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogenated pyridines and 1,8-naphthyridines. VI.The principle of the synthesis of 3-halomethyl-2,6-dichloro-pyridines has been extended to compounds with side chains of more than one carbon atom in the 3-position. Feasible synthetic routes are outlined starting from cheap, commercially available α-methylideneglutaronitrile and trichloroalkyl functional compounds which yield the intermediate 1,3,5-trisubstituted alkanes. These are cyclized by aqueous mineral acid or by hydrogen bromide in an organic solvent to 2-substituted glutarimids or hexahydronaphthyridinones, depending on the mode of cyclization. The final aromatization provides a simple route to pyridines or 1, 8-naphthyridines.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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