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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 862-882 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Diels-Alder Reactivity of s-tis-Fixed 1,3-DienesContrary to the 1,2-dimethylenecycloalkanes 8-10 and 2,3-dimethylene-14-dioxane (6), the 4,5-dimethylene-1,3-dioxolanes 1-5 show very poor diene reactivities in the Diels-Alder reaction though possessing an s-cis-fixed diene system. This is documented by bimolecular rate constants as well as activation parameters. The influence of the ionisation potentials measured by PE spectroscopy and of the molecular geometries calculated by the MINDO/3 method on the reactivity is studied. It is shown that not the dehedral angle but the scissoring (1.4-distance) of the diene system is of decisive importance for the reactivity of the s-cis-fixed dienes.
    Notes: Die 4,5-Dimethylen-1,3-dioxolane 1-5 zeigen, obwohl sie s-cis-fixierte Diensysteme darstellen, im Vergleich zu den 1,2-Dimethylencycloalkanen 8-10 und 2,3-Dimethylen-1,4-dioxan (6) sehr geringe Dienreaktivitäten, wie durch die Geschwindigkeitskonstanten und die Aktivierungsparameter belegt wird. Der Einfluß der durch Photoelektronenspektroskopie festgelegten Ionisationspotentiale und der nach dem MINDO/3-Verfahren berechneten Molekülgeometrien auf die Reaktivität wird untersucht. Es zeigt sich, daß für die Reaktivität der s-cis-fixierten Diene nicht der Interplanarwinkel, sondern die Scherung (1,4-Abstand) des Dien-Systems von entscheidender Bedeutung ist.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1977 (1977), S. 27-32 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 4,5-Dimethyl-1,3-dioxolan-2-one4,5-Dimethylene-1,3-dioxolan-2-one (2) can be prepared in a three step synthesis starting from the diastereomeric 4,5-dimethyl-1,3-dioxolan-2-one (4). The Fe(CO)3-complex 7 and the parent compound 2 are stable; however, they show enhanced reactivity compared to structurally analogous compounds. 7 is sensitive towards oxygen and 2 polymerises spontanously above the melting point (48°C). The dienophilic reactivity of 2 is very poor.
    Notes: 4,5-Dimethylen-1,3-dioxolan-2-on (2) läßt sich aus den diastereomeren 4,5-Dimethyl-1,3-dioxolan-2-onen (4) in einer dreistufigen Synthese herstellen. Der Fe(CO)3-Komplex 7 und die freie Verbindung 2 sind beständig, jedoch im Vergleich zu strukturanalogen Verbindungen reaktiver. 7 ist empfindlich gegen Luftsauerstoff; 2 polymerisiert oberhalb des Schmelzpunktes (48°C) spontan. Die dienophile Reaktivität von 2 ist sehr gering.
    Additional Material: 2 Tab.
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