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  • 1985-1989  (3)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 50 (1985), S. 2438-2443 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 118 (1985), S. 634-642 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Carbene Reactions, XVII Nitrile Ylides via 1,1-EliminationThe 3-aminoquadricyclane-3-carbonitrile 7 decomposed upon vapor phase thermolysis into benzene and cyano(dimethylamino)carbene 15. Thermolysis of the corresponding benzylidene derivative 20 liberated the 1,3-dipole 21, which eventually leads to 1-isoindolecarbonitrile 23. The nitrile ylide 26 liberated similarly furnished the bicyclic compound 27 via intramolecular 1,3-dipolar addition.
    Notes: Das 3-Aminoquadricyclan-3-carbonitril 7 zerfällt bei der Gasphasenthermolyse in Benzol und Cyan(dimethylamino)carben 15. Die entsprechende Benzylidenverbindung 20 setzt bei der Thermolyse den 1,3-Dipol 21 frei, der sich zum 1-Isoindolcarbonitril 23 stabilisiert. Das analog freigesetzte Nitrilylid 26 ergab durch intramolekulare 1,3-dipolare Cycloaddition den Bicyclus 27.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 119 (1986), S. 3297-3315 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Carben-Reaktionen, XX. Strukturelle Voraussetzungen für die Thermische Abspaltung von Carbenen aus NorbornadienenEin Konzept wird vorgestellt, wonach Norbornadiene mit schwachen Donor-Substituenten an C-7 beim Erhitzen eine Homolyse der C-1/C-7-Bindung erleiden. Diese führt über das Diradikal 6 zu Cycloheptatrienen oder zu Benzyl-Verbindungen. Dagegen sollen Norbornadiene, die an C-7 ausgeprägte Donor-Systeme tragen, eine Heterolyse der C-1/C-7-Bindung erleiden, worauf das so gebildete Zwitterion 7 direkt ein Carben im Singulett-Grundzustand abspaltet.
    Notes: The notion is put forward that norbornadienes having weak donor substituents at C-7 should suffer homolysis of the C-1/C-7 bond on heating, leading via the diradical 6 to either cycloheptatrienes or benzylic compounds. In contrast, norbornadienes having strong donor systems at C-7 should suffer heterolysis of the C-1/C-7 bond, whereupon the resulting zwitterion 7 collapses directly to carbenes in a singlet ground state.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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