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Showing 1 to 6 of 6 for “"Aminoalkohole"”.

  1. 1,3-Aminoalkohole als Bausteine in der asymmetrischen Synthese von Azetidinen, Azetidincarbonsäuren und Piperidin-3-olen

    Four-membered cyclic amines – the azetidines – are an original class of compounds with limited occurrence in nature. Nevertheless enantiopure azetidines and in particular derivatives of the azetidine-2-carboxylic acid are used in medicine, crop protection and asymmetric catalysis. Despite these …

    aachen Repository record for 1,3-Aminoalkohole als Bausteine in der asymmetrischen Synthese von Azetidinen, Azetidincarbonsäuren und Piperidin-3-olen (opens in a new tab)

  2. Katalytische, enantioselektive Synthesen von Diarylmethanolen und Allylalkoholen

    In this research new, catalytic, enantioselective aryl transfer reactions to aldehydes for the synthesis of chiral diarylmethanols were developed. Diarylmethanols are important intermediates for the synthesis of pharmaceutically active compounds. In the foregoing research, it was found that, in …

    aachen Repository record for Katalytische, enantioselektive Synthesen von Diarylmethanolen und Allylalkoholen (opens in a new tab)

  3. Enantioselective synthesis of cyclic beta-amino alcohols via tandem hydroalumination-cyclization-reduction of ethoxycarbonyl vinyl sulfoximines and application to the synthesis of potential aggrecanase inhibitors

    The beta-amino alcohol moiety is a common structural component in a wide variety of natural occurring compounds, synthetic pharmacologically important molecules, ligands and chiral auxiliaries for asymmetric synthesis. Due to the fact that the stereochemistry of the beta-amino alcohol moiety is …

    aachen Repository record for Enantioselective synthesis of cyclic beta-amino alcohols via tandem hydroalumination-cyclization-reduction of ethoxycarbonyl vinyl sulfoximines and application to the synthesis of potential aggrecanase inhibitors (opens in a new tab)