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  • 2005-2009
  • 1985-1989
  • 1960-1964  (2)
  • 1964  (2)
  • Cyclooctatetraenes  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 83-85 
    ISSN: 0570-0833
    Keywords: Valence tautomerism ; Cyclooctatetraenes ; Bicyclooctatriene ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Diels-Alder adducts of cyclooctatetraene and its derivatives are derived from the bicyclo[4,2,0]octane structure. A kinetic investigation shows that the Diels-Alder addition of dienophiles to cyclooctatetraene and phenylcyclooctatetraene is preceded by a valence tautomerism equilibrium with bicyclo[4,2,0]octa-2,4,7-triene or its 7-phenyl derivative.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 185-191 
    ISSN: 0570-0833
    Keywords: Coordination modes ; Catalysis ; Cyclooctatetraenes ; Reppe chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relationship between the structure and the catalytic activity of nickel(II) complexes in the synthesis of cyclooctatetraene by the method of W. Reppe is discussed. The cyclotetramerization of acetylene takes place within labile Ni(II)-acetylene π-complexes. Inhibition tests have made it probable that four molecules of acetylene are grouped around the nickel ion in the transition state, in a configuration which favors the formation of the eight-membered ring.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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