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  • 1975-1979  (22)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Accounts of chemical research 9 (1976), S. 364-371 
    ISSN: 1520-4898
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 100 (1978), S. 7066-7068 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 99 (1977), S. 1669-1670 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 64 (1977), S. 397-402 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Notes: Abstract In this article several compounds with unusual ring systems are surveyed briefly. Saturated and unsaturated monocyclic compounds, polycyclic compounds, and unconventional aromatic systems are covered. The reasons for the interest of organic chemists in the unusual ring systems are discussed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 199-207 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vinyl Cations, 24. A [1,2]-Hydride Shift in the Solvolysis of Phenylvinyl Trifluoromethanesulfonates(E)- and (Z)-1-methyl-2-phenylvinyl trifluoromethanesulfonate (3E, 3Z) and 1-benzylvinyl trifluoromethanesulfonate (4) have been synthesized. Their products of solvolysis were identified and their rates of solvolysis determined in various 2,2,2-trifluoroethanol/water mixtures. Solvolysis of 3E and 3Z leads, besides other products, to ethyl phenyl ketone (9), demonstrating a [1,2]-hydride shift across the double bond in the initially formed vinyl cation 10. In the solvolysis of 4, a [1,2]-hydride shift towards the double bond has not been found.
    Notes: (E)- und (Z)-1-Methyl-2-phenylvinyl-trifluormethansulfonat (3E, 3Z) und 1-Benzylvinyl-trifluormethansulfonat (4) wurden dargestellt, ihre Solvolyseprodukte aufgeklärt und die Solvolyse-geschwindigkeiten in verschiedenen 2,2,2-Trifluorethanol/Wasser-Gemischen bestimmt. Bei der Solvolyse von 3E und 3Z entstand neben anderen Produkten Ethylphenylketon (9), wodurch im zunächst entstehenden Vinylkation 10 eine [1,2]-Hydridwanderung über die Doppelbindung hinweg nachgewiesen wurde. Eine [1,2]-Hydridverschiebung in Richtung auf die Doppelbindung konnte bei der Solvolyse von 4 nicht gefunden werden.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 2212-2218 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vinyl Cations, 20. Synthesis and Solvolysis of Bicyclo[5.3.0]dec-l-ene-2-yl TriflateBicyclo[5.3.0]dec-1-ene-2-yl triflate (6) and Δ1(8a)-octalinyl triflate (7) were synthesized and the solvolyses of both compounds were investigated in different solvents. 6 reacts in 50% aqueous ethanol and in 70% trifluoroethanol mostly with rearrangement to 1-decalone (3). Similarly, a rearrangement to the octalinyl system occurs in absol. TFE, in which the enol ether 11 is formed. In contrast, 7 solvolyses in the same solvents mostly with retention of structure. A rearrangement to the bicyclo[5.3.0]decane system was observed only in small amounts. - The triflate 6 solvolyses in 50% aqueous ethanol 343 times faster than 7. The product analyses as well as the kinetics show that the solvolyses occur via vinyl cation intermediates. The octalinyl cation 2 would appear to have a higher stability than the bicyclic vinyl cation 4.
    Notes: Bicyclo[5.3.0]dec-1-en-2-yl-triflat (6) und Δ1(8a)-Octalin-1-yl-triflat (7) wurden synthetisiert und ihre Solvolysereaktionen in verschiedenen Lösungsmitteln untersucht. 6 reagiert in 50proz. wäßr. Äthanol und in 70proz. Trifluoräthanol weitgehend unter Umlagerung zum 1-Decalon (3). In absol. Trifluoräthanol tritt ebenfalls Umlagerung in das Octalinylsystem ein, wobei der Enoläther 11 erhalten wird. 7 solvolysiert in den gleichen Lösungsmitteln weitgehend unter Strukturerhaltung, eine Umlagerung in das Bicyclo[5.3.0]decan-System wird nur in untergeordnetem Maße beobachtet. - Das Triflat 6 solvolysiert in 50proz. wäßr. Äthanol 343 mal schneller als 7. - Die Produktanalysen sowie die Kinetik zeigen, daß die Solvolysen über Vinyl-Kationen ablaufen, wobei das Octalinyl-Kation 2 sich durch eine höhere Stabilität gegenüber dem bicyclischen Vinyl-Kation 4 auszeichnet.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1253-1263 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vinyl Cations, 26: Syntheses and Solvolyses of Vinyl FluoridesThe vinyl fluorides 5-8 were prepared by treatment of the corresponding olefins with BrF and subsequent dehydrobromination. The solvolysis reactions in various solvents were studied. The products and their rates of solvolysis measured under different conditions point to a vinyl cation mechanism of the solvolysis reactions.
    Notes: Die Vinylfluoride 5-8 wurden durch Umsetzung der entsprechenden Olefine mit BrF und sich anschließende Dehydrobromierung dargestellt und die Solvolysereaktionen in mehreren Lösungsmitteln untersucht. Die Reaktionsprodukte sowie die unter verschiedenen Bedingungen gemessenen Solvolysegeschwindigkeiten deuten auf einen Verlauf der Solvolyse über Vinylkationen.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 2453-2464 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vinyl Cations, 31. Synthesis and Solvolysis of (Bromocyclopropylmethylene)cyclopropane(Bromocyclopropylmethylene)cyclopropane (3f) has been synthesized by bromination of (cyclo-propylmethylene)cyclopropane (14) and subsequent dehydrobromination. The solvolysis of 3f was investigated in solvents of various ionizing power. The reaction products and the solvolysis rates including salt effects show that the solvolysis proceeds via a vinyl cation mechanism involving intimate- and solvent separated ion pairs and dissociated ions.
    Notes: (Bromcyclopropylmethylen)cyclopropan (3f) wurde durch Bromierung von (Cyclopropyl-methylen)cyclopropan (14) und anschließende Dehydrobromierung dargestellt. Die Solvolyse von 3fwurde in Lösungsmitteln verschiedener Ionisierungsstärke untersucht. Die Reaktionsprodukte sowie die Solvolysegeschwindigkeit unter Einbeziehung von Salzeffekten zeigen, daβ die Solvolyse über einen Vinylkationenmechanismus unter Beteiligung von inneren und äußeren Ionenpaaren sowie von freien Ionen abläuft.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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