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  • Organic Chemistry  (1)
  • Sensory imbalance  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Control of turning behavior under apomorphine by sensory input from the face (1992)
    Springer
    Psychopharmacology 109 (1992), S. 390-394 
    Details
    ISSN: 1432-2072
    Keywords: Apomorphine ; Turning behavior ; Sensory imbalance ; Sensory responsiveness ; Dopamine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract It has been shown that peripheral manipulation of sensory input by removal of vibrissae on one side of the rat's face induces turning behavior which is directed towards the contralateral vibrissae-intact side, under the influence of the dopamine receptor agonist apomorphine. In the present experiment, we examined whether rats under apomorphine turn towards the side with more sensory input, or simply away from the manipulated side. Thus, an experimental manipulation was designed to increase sensory input. Sensory stimulation was applied by attaching a clip into the fur on one side of the face. Rats injected with apomorphine in doses of 0.5–5.0 mg/kg (but not with 0.05 mg/kg or vehicle) exhibited turning behavior towards the side of the clip. This sensory stimulation was also found to influence spontaneous behavioral asymmetries. These results show that an imbalance in sensory input is sufficient to produce turning under apomorphine.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02247713
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  • 2
    Electronic Resource
    Electronic Resource
    Herstellung von ‘Semialdehyd’-Derivaten von Asparaginsäure- und Glutaminsäure durch Rosenmund-Reduktion (1990)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 73 (1990), S. 405-410 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation of ‘Semialdehyde’ Derivatives of Aspartic and Glutamic Acid via the Rosenmund ReductionSuitably protected aspartic-acid ‘β-semialdehyde’ and glutamic-acid ‘γ-aldehyde’ derivatives can be obtained, in good yield by Rosenmund reduction of the corresponding acid chlorides. Benzyloxycarbonyl (Z) and (tert-butoxy)carbonyl (Boc) protecting groups are not affected under these reaction conditions. The sensitive aldehydes, which are obtained in higher purity than by hydride reductions, can directly be used for further transformations like aldol-type reactions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19900730219
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    Paper (German National Licenses)
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