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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1982 (1982), S. 924-929 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1,3-Dipolar Cycloadditions of 3,4-Dihydro-6,7-dimethoxyisoquinolinium Salts1,3-Dipolar cycloadditions of 3,4-dihydro-6,7-dimethoxyisoquinolinium salts3 with 6,7-dialkoxy-3,4-dihydroisoquinolines 1 have been investigated. Dependent on the structure of both the dipolarophiles and the dipoles, cycloadducts of exo- and/or endo type are formed. The exo/endo ratio depends on temperature.
    Notes: Die 1,3-dipolaren Cycloadditionen von 3,4-Dihydro-6,7-dimethoxyisochinoliniumsalzen 3 mit 6,7-Dialkoxy-3,4-dihydroisochinolinen 1 wurden untersucht. Es bilden sich Cycloaddukte vom exo- und/oder endo-Typ in Abhängigkeit von der Struktur des Dipolarophils und des Dipols. Das exo/endo-Verhältnis ist temperaturabhängig.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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