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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 729 (1969), S. 52-63 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Ally1 Alcohols with Active Methine and Methylene Compoundsγ.δ-Unsaturated ketones 4 are intermediates in several syntheses of natural products. They may be obtained from allyl alcohols and β-keto esters. Novel synthetic approaches to γ.δ-unsaturated ketones 4 and the related compounds 12, 14, 16, and 18 are described (tables 7-10). The investigations lead to a new synthetic route for the preparation of the juvenile hormone (10).
    Notes: γ.δ-Ungesättigte Ketone 4, herstellbar aus Allylalkoholen und β-Ketoestern, sind Zwischenprodukte verschiedener Naturstoff-Synthesen. Es werden neue Synthesemöglichkeiten von 4 und den damit verwandten Verbindungen 12, 14, 16 und 18 (Tabb. 7 - 10) beschrieben. Die Arbeiten führen zu einem Herstellungsverfahren des Juvenilhormons (10).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 72 (1960), S. 865-865 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 529 (1937), S. 68-83 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 747 (1971), S. 60-69 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Reactions of 6,10-Dimethyl-3,5,10-undecatrien-2-onesIn contrast to pseudoionone 2 the isomer 1 and its methylhomologues may be obtained directly without formation of by-products by reacting 7-octen-1-yne-3-ols 6 with esters of acetoacetic acid or diketene. On addition of carboxylic acids the cis,trans- and trans,trans isomers are formed preferably. Starting with 1, a new cyclization reaction leads to the unknown ionone isomers 14 and 15.
    Notes: Im Gegensatz zu Pseudojonon 2 können das Isomere 1 und dessen Methylhomologe direkt durch Umsetzung substituierter 7-Octen-1-in-3-ole 6 mit Acetessigestern oder Diketen ohne Bildung störender Nebenprodukte hergestellt werden. Bei Zusatz organischer Säuren werden bevorzugt die cis.trans- und trans.trans-Formen gebildet. Von 1 ausgehend führt eine neuartige Cyclisierung zu den bisher unbekannten Jonon-Isomeren 14 bzw. 15.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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