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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 6 (1967), S. 666-677 
    ISSN: 0570-0833
    Keywords: Neighboring-group effects ; Rearrangement ; Homoallyl systems ; Strained molecules ; Cyclobutanes ; Cyclopropanes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The neighboring-group effect produced by a double bond in the homoallyl position or by a cyclopropane or cyclobutane ring leads to interesting rearrangements, which are discussed in this paper mainly from the point of view of mechanism, but also from that of preparative work. The question of the postulated non-classical carbonium ions acquires a special significance in this connection.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 8 (1969), S. 410-420 
    ISSN: 0570-0833
    Keywords: Rearrangement ; Organometallic compounds ; Arene ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: σ-Bonded organic groups in transition-metal complexes can rearrange to π-bonding ligands and vice versa: the classic example is the formation of π-arenechromium complexes from σ-arylchromium compounds. Rearrangements of this kind can be induced, inter alia, by reactions of the metal or of the ligand, as well as by migration or insertion of a ligand. Rearrangements play a role in many industrial processes, including the polymerization and isomerization of olefins and the hydroformylation of olefins.
    Additional Material: 2 Ill.
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  • 3
    ISSN: 0570-0833
    Keywords: Memory effects ; Stereochemistry ; Rearrangement ; Carbocations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereochemical configuration at the initial site of heterolysis in a carbonium ion process in solution controls the specificity of migration two steps later in many sequential multiple rearrangements. These “memory effects” are attributable to the presence on the potential energy surface of small, hitherto undetectable minima. A variety of structural, stereochemical, and isotopic marking techniques are used to demonstrate that memory effects are a general feature of the ring-expansion route to bicyclic carbonium ions. The intermediates formed in these reactions, although necessarily symmetrical or quasi-symmetrical at equilibrium, act unsymmetrically. The memory effect uses the rate of an intramolecular carbonium ion rearrangement as a calibration with which to compare the rate of symmetrization. In this way, the system functions as a sensor of sub-species.
    Additional Material: 3 Ill.
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  • 4
    ISSN: 0570-0833
    Keywords: Valence isomerization ; Bullvalene ; Rearrangement ; Cyclooctatetraenes ; Homotropilidene ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Compounds which undergo fast and reversible valence-bond isomerization (i.e. which have fluctuating cyclopropyl and/or double bonds) are taken to be those in which the average life-time of the valence-bond isomers at 0 °C is of the order of 100 seconds at most, and for which the maximum activation energy of the bond migration is 20 kcal/mole. The fast, reversible bond shift can scarcely be detected by chemical means, but can be recognized by NMR spectroscopy, since the time for which a proton occupies a position with a given magnetic environment has a pronounced influence on the NMR spectrum. Some examples of molecules with fluctuating bonds are cyclooctatetraene and its derivatives, unsaturated seven- membered ring systems, homotropilidene, bridged homotropilidene systems, bullvalene, and substituted bullvalenes. The last class is particularly interesting, since here the carbon atoms are continually changing their relative positions and neighbors.
    Additional Material: 2 Ill.
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