Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 93 (1992), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Fatty acid composition was analysed in the producer of avermectins, Streptomyces avermitilis C-18 grown in chemically defined medium with different nitrogen sources. Significant differences in nitrogen regulation of fatty acid biosynthesis were found in this strain in comparison with other streptomycetes studied so far. This finding could be explained at the level of regulation of branched-chain amino acid metabolism.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 125 (1994), S. 901-908 
    ISSN: 1434-4475
    Keywords: Arenetricarbonylchromium Complexes ; Rapid Synthesis ; Solvent and Catalyst Effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Es wurde der Effekt von 8 Lösungsmitteln auf Komplexierungsgeschwindigkeit und Ausbeute der Komplexbildung von Toluol mit Cr(CO)6 untersucht. Dabei wurde festgestellt, daß die Intensität der Erhitzung beim Sieden in einigen Fällen einen wesentlichen Effekt auf die Komplexierungsgeschwindigkeit hat (bein-Hexanol, Cyclohexanon und Diglyme). Die Komplexierungsgeschwindigkeit ist in diesen Fällen die größte, die bereits beträchtlich einsetzende Zersetzung ergibt aber geringere Ausbeuten. Butylacetat, Dibutylether und Decalin erwiesen sich als die günstigsten Lösungsmittel. Außerdem wurden 27 verschiedene Katalysatoren für die Komplexierungsreaktion in Decalin als Lösungsmittel getestet und ihre Effizienz durch Geschwindigkeitskonstanten und isolierbare Ausbeute charakterisiert. Die Geschwindigkeitskonstanten wurden aus der Entwicklung von CO berechnet; sie liegen zwischen 6.5·10−5 s−1 für Ameisensäure bis zu 6.5·10−4 s−1 für Ethylacetamidomalonat. Cycloalkanone erwiesen sich als die besseren Katalysatoren gegenüber acyclischen Ketonen vergleichbaren Siedepunkts. Lactone sind effektvoller als Ester, cyclische sowohl als auch acyclische Ketone und Diester mit ähnlichen Siedepunkten.
    Notes: Summary The effect of 8 solvents on the rate as well as the yields of complexation of toluene with Cr(CO)6 has been studied. It has been found that the intensity of boiling has a profound effect on the rate of complexation in some cases (whenn-hexanol, cyclohexanone or diglyme is used as solvent). The rates of complexation are highest in these cases, but a considerable extent of decomposition results in lower yields. Butyl acetate, dibutyl ether and decalin have been found to be the most feasible solvents. Additionally, 27 different catalysts have been tested for the complexation of toluene in decalin solution, their effect being quantified by rate constants and the isolated yields of the reaction. The rate constants have been obtained from the rate of CO evolution and vary from 6.6·10−5 s−1 for formic acid to 6.5·10−4 s−1 for ethyl acetamidomalonate. Cycloalkanones proved to be more efficient catalysts than acyclic ketones with a close boiling point. Lactones are more efficient than esters, both cyclic and acyclic ketones, and diesters, all having a similar boiling point.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Brain topography 4 (1991), S. 37-46 
    ISSN: 1573-6792
    Keywords: Acupuncture ; Tactile stimulation ; Somatosensory cortex ; Dipole tracing ; Afferent inhibition ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of acupuncture and tactile skin stimulation on somatosensory evoked potentials (SEPs), elicited by the median nerve stimulation, were investigated in healthy subjects. Acupuncture needles were inserted into either Hegu plus Shousanli, Hegu plus Waiguan, or Shousanli positions ipsilateral to the median nerve stimulation. Tactile skin stimulation was applied to either the ulnar side of the palm, or the dorsal surface of the hand or forearm ipsilaterally to the nerve stimulation. It was found that acupuncture significantly suppressed the amplitude of P22 and P40, and that the tactile skin stimulation of the ulnar side of the palm significantly suppressed the amplitude of P22 and P40, but that the peak latencies were not affected. Dipole tracing analysis showed that the location and vector direction of P22 were not changed but the vector moment of P22 was changed by both acupuncture and tactile stimulation. Based on these findings the suppressive effect of acupuncture and skin stimulation on P22 was proposed to be due to the afferent inhibition in the somatosensory cortex. Although the suppressive mechanism of P40 by tactile skin stimulation seemed to be similar to that of P22, the suppression of P40 by acupuncture appeared to include different mechanisms.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 14 (1980), S. 138-140 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H NMR spectra of 26 substituted chalcones (3-aryl-1 phenyl-2-propene-1-ones and 1-aryl-3-phenyl-2-propene-1-ones) have been studied. The chemical shifts of the α and β protons to the carbonyl group were correlated with Hammett s̰ parameters. To gain information on the effect of the transmission of the resonance and inductive contributions of the substituents on the chemical shifts of H-α and H-β, two parameter correlations with f and r parameters were also perfomed. The chemical shifts of the aromatic protons of the para-disubstituted benzene ring correlated with the ai substituent increments.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C and 1H chemical shifts of the ferrocene moiety, as well as the carbonyl carbons and styrene moiety, of substituted 2-benzylidene[3]ferrocenophane-1,3-diones have been assigned. Correlations of 13C substituent chemical shifts of both carbonyl carbons with the Hammett constants have been found, and the effect of the transmission of substituent effects on these chemical shifts through the styrene moiety is discussed. An explanation is given for the different sensitivities of the carbonyl carbon chemical shifts to the electronic effect of substituents in mono- and dicarbonyl derivatives.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 14 (1980), S. 181-185 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The transmission of electronic effects across the ferrocene analogues of chalcones [3-aryl-1-ferrocenyl-2-propene-1-ones (series 1) and 1-aryl-3-ferrocenyl-2-propene-1-ones (series 2)], as well as the conformations of both types of ferrocene analogues have been studied. The ferrocene analogues of chalcones of series 1 were found to be in a non-planar conformation. Their H-α and C-α chemical shifts are more sensitive to the resonance than to the inductive effects of substituents. The C-α chemical shifts of the ferrocene analogues of chalcones of series 2 are more sensitive to the inductive than to the resonance effects of substituents. The transmission of the substituent effects to the ferrocene moiety is also briefly discussed.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...