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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 100 (1978), S. 3945-3946 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-0638
    Source: Springer Online Journal Archives 1860-2000
    Topics: Education
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1272-1279 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thermal Rearrangements of 8-Methoxybicyclo[5.1.0]octa-2,4-diene and 8-Methoxybicyclo[5.1.0]oct-2-eneThe equilibria 2x ⇄ 3e and 9x ⇄ 11 of the title compounds reveal a slight influence of methoxy substituents on the stability of cyclopropane rings. Reactions which involve the distal cyclopropane bond  -  the butadienylcyclopropane rearrangement of 2 and the homo-1,5-H shift of 9  -  are but modestly accelerated by methoxy groups. The vinylcyclopropane rearrangement 9x → 10 confirms the strong methoxy effect on proximal cyclopropane bonds.
    Notes: Die Gleichgewichte 2x ⇄ 3e und 9x ⇄ 11 der Titelverbindungen zeigen einen geringen Einfluß von Methoxy-Substituenten auf die Stabilität des Cyclopropanrings. Reaktionen unter Beteiligung der gegenüberliegenden Cyclopropan-Bindung  -  die Butadienylcyclopropan-Umlagerung von 2 und die Homo-1,5-H-Verschiebung von 9  -  werden durch Methoxygruppen nur mäßig beschleunigt. Die Vinylcyclopropan-Umlagerung 9x → 10 bestätigt den starken Methoxy-Effekt auf benachbarte Cyclopropan-Bindungen.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 3711-3721 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Deamination Reactions, VIII. Ring Opening of Bicyclo[n.1.0]alkyldiazonium IonsBicyclo[5.1.0]oct-8-yldiazonium ions (7) were generated by alkaline cleavage of the corresponding exo- and endo-nitrosoureas 6a and b. Both starting materials afforded exclusively trans-cyclooctenyl derivatives (9, 10). In deuterated solvents, 7b (endo) reacted with incorporation of approximately 1 g-atom D/mole whereas deuterium incorporation with 7a (exo) was only 0.3 - 0.4 g-atom D/mole. Bicyclo[3.1.0]hex-6-yldiazonium ions (19a, b) yielded exclusively cyclohexenyl derivatives (22, 23). In this case, deuterium incorporation of the exo isomer (19a) was greater than that of the endo-isomer (19b). The result indicate that diazonium ions capable of concerted reaction (7a, 19b). decompose more rapidly than their isomers 7b and 19a. The latter undergo base-catalyzed isomerization before they decompose; in deuterated solvents this process is accompanied by incorporation of deuterium.
    Notes: Bicyclo[5.1.0]octyl-(8)-diazonium-Ionen (7) wurden durch alkalische Spaltung des exo- und endo-Nitrosoharnstoffs 6a und b erzeugt. Beide Ausgangsmaterialien ergaben ausschließlich trans-Cyclooctenylderivate (9, 10). In deuterierten Lösungsmitteln verlief die Umsetzung von 7b (endo) unter Einbau von nahezu 1 g-Atom D/Mol, während der Deuterium-Einbau bei 7a (exo) nur 0.3-0.4 g-Atom D/Mol betrug. Bicyclo[3.1.0]hexyl-(6)-diazonium-Ionen (19a und b) lieferten ausschließlich Cyclohexenylderivate (22, 23). Hier war der Deuterium-Einbau beim exo-Isomeren (19a) höher als beim endo-Isomeren (19b). Die Ergebnisse legen nahe, daß die zum Synchron-Zerfall befähigten Diazonium-Ionen 7a und 19b rascher zerfallen als ihre Isomeren 7b und 19a. Letztere erfahren vor dem Zerfall eine basenkatalysierte Isomerisierung, die in deuterierten Lösungsmitteln mit Deuterium-Einbau verbunden ist.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 1856-1867 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Rearrangement of Bicyclo[5.1.0]octa-2,4-diene Derivatives by AcidsThe addition of acids to bicyclo [5.1.0] octa-2,4-dienes mat proceed with rearrangement to bicyclo-[3.2.1] oct-2-enes. A donor substituent at C-8 is essential for this transformation, as shown by the decreasing tendency of 1 (NHCOCH3), 19 (OCH3), and (33) H) to form bicyclo [3.2.1] octenes. Cycloheptadienylmethyl derivatives are formed in a competing reaction. Regardless of the configuration of the starting material (19a, b), 4-exo-8-anti-substituted bicyclo [3.2.1] oct-2-enes are obtained. Configurations were established by n. m. r. and by unequivocal synthesis of 25. The reaction is thought to involve protolysis of the cyclopropane ring to a homoallyl cation 36 which undergoes cyclization to 38 (formally a 1,4 shift).
    Notes: Die Addition von Säuren an Bicyclo[5.1.0] octa-2,4-diene kann unter Umlagerung zu Bicyclo [3.2.1] oct-2-enen verlaufen. Ein Donor-Substituent an C-8 ist Voraussetzung für diese Umwandlung, wie aus der abnehmenden Tendenz von 1 (NHCOCH3), 19 (OCH3) und 33 (H) zur Bildung von Bicylo [3.2.1] octenen hervorgeht. In einer konkurrierenden Reaktion entstehen Cycloheptadienylmethyl-Derivate. Unabhängig von der Konfiguration des Ausgangsmaterials (19a, b) werden 4-exo-8-anti -substituierte Bicyclo [3.2.1.] oct-2-ene erhalten. Die Konfigurationen wurden durch NMR und eindeutige Synthese von 25 festgelegt. Die Reaktion beginnt wahrscheinlich mit der Protolyse des Cyclopropanrings zum Homoallylkation 36, das zu 38 cyclisiert (formal eine 1,4-Verschiebung).
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 83 (1971), S. 251-252 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 10 (1971), S. 263-264 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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