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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 9 (1986), S. 308-309 
    ISSN: 0935-6304
    Keywords: High performance liquid chromatography, HPLC ; Reverse phase ; Internal standard ; Trimellitic anhydride ; Air sample ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0170-2041
    Keywords: Resolution, kinetic ; Chiral tertiary amines ; Chiral esters ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kinetic Resolutions Starting with rac-Alcohols or rac-Acyl Halides Using Optically Active Inductor BasesIn the reaction of one mole equivalent of achiral acyl halides with two equivalents of rac-alcohols in the presence of one equivalent of an optically active inductor base (tertiary amine) partially optically active esters and partially optically active alcohols are formed, having in some cases high optical purity (60 - 70%). The alcohol moiety of the ester and the unchanged alcohol are of opposite configuration. Treatment of two equivalents of rac-acylhalides with one equivalent of an achiral alcohol and an inductor base also leads to a high degree of optical induction. The carbonic acid moiety in the ester and the unchanged acid are of opposite configuration. The optical induction is influenced a) by the ligands linked to the reaction centers, b) by the relative quantities of the reacting partners, c) by the solvent, and d) by the temperature.
    Notes: Bei der Umsetzung eines Moläquivalents achiraler Carbonsäurehalogenide mit zwei Moläquivalenten rac-Alkoholen entstehen unter Mitwirkung von einem Moläquivalent einer optisch aktiven Induktorbase (tertiäres Amin) partiell optisch aktive Ester sowie partiell optisch aktive Alkohole in zum Teil hoher optischer Reinheit (60 - 70%). Der im Ester gebundene Anteil an Alkohol sowie der nicht umgesetzte Alkohol haben entgegengesetzte Konfiguration. Der Induktionsgrad ist ähnlich hoch, wenn man zwei Moläquivalente eines rac-Carbonsäurehalogenids mit je einem Moläquivalent eines achiralen Alkohols und einer Induktorbase umsetzt. Der Carbonsäureanteil im Ester und die freie Säure haben entgegengesetzte Konfiguration. Die optischen Induktionen werden beeinflußt a) durch die Art der mit den Reaktionszentren verknüpften Liganden, b) durch die relativen Mengen der Reaktionspartner, c) durch das Lösungsmittel und d) durch die Temperatur.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman (3500-20 cm-1) and infrared (3500-50 cm-1) spectra of gaseous and solid methylcyclobutane and methyl-d3-cyclobutane have been recorded. Additionally, the Raman spectra of the pure liquids have been recorded and qualitative depolarization values have been obtained. The spectra have been interpreted on the basis that both the axial and equatorial conformers are present in the fluid phases and that the equatorial form is thermodynamically preferred and the only form present in the annealed solid. All 39 of the normal vibrational modes have been assigned for both the d0 and d3 compounds. An abundance of spectral evidence is presented which indicates extensive coupling between the vibrations associated with the ring and those of the methyl group. The CH3 internal torsional mode has been observed in the Raman spectrum of the solid at 232 cm-1 and utilizing this frequency the periodic threefold barrier to internal rotation has been calculated to be 1190 cm-1 (3.40 kcal mol-1). The fundamental ring puckering mode has been assigned from the Raman spectra of the gases to weak features observed at 161 and 154 cm-1 for the d0 and d3 compounds, respectively. All of these results are compared with the corresponding quantities for some similar molecules.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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