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  • 1980-1984  (2)
  • 1981  (1)
  • 1980  (1)
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  • 1980-1984  (2)
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  • 1
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract The anodic oxidation of N-anions of diacylimides which are acidic enough to be deprotonated by relatively weak bases in protic solvents was investigated with respect to the electrode kinetics and preparative aspects. All imide anions are oxidized in a one-electron step to the respective imide radicals. Of the imides investigated, two were cyclic carboxylic imides (succinimide and phthalimide) three were sulphonyl imides (di-p-toluene and di-benzene sulphimide, dimethane sulphimide) and one was a mixed carboxylate-sulphonate imide (saccharate). The imide radicals produced by anodic oxidation of the dicarboxylate imides do not couple to form a hydrazine derivative but induce solvent oxidation by H-abstraction. The disulphonyl imides couple to unstable hydrazine derivatives although H-abstraction occurs to more than 80%. Only the anodic coupling of the N-anion of imido-disulphonic acid to hydrazine tetrasulphonate discovered by Grinstead [3] can be performed with good selectivity and current and mass yields. The optimum conditions for this reaction are determined in order to show that it may serve in the future as one step in a new hydrazine process.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1041
    Keywords: lisuride ; prolactin ; plasma levels ; halflife ; pharmacokinetics ; dopamine agonist
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The development of a sensitive radioimmunoassay for the determination of lisuride in plasma is described. The antiserum against lisuride-4-hemisuccinate-BSA was raised in rabbits. Using this method the plasma levels of lisuride were monitored following one intravenous (25 µg) and two oral (100 µg and 300 µg) doses of lisuride hydrogen maleate in three female and three male volunteers (intraindividual comparison). The plasma prolactin was also determined by radioimmunoassay. Following i. v. injection, the concentration of lisuride declined in three phases, with half-lives of 5 min, 25 min and 2 h. The total plasma clearance of 800±250 ml × min−1 was in the range of “plasma flow” through the liver. In agreement with the high rate of biotransformation, the bioavailability of lisuride administered orally was 10%±7% of the 100-µg dose, and 22%±7% of the 300-µg dose. The plasma prolactin was lowered to 3%–18% of its pretreatment value depending on the route of administration and the dose. The reduction appeared to be short-lived and to be directly dependent on the plasma concentration of lisuride. Following intravenous injection, the prolactin level declined after a so far unexplained lagtime of 0.5 h.
    Type of Medium: Electronic Resource
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