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Showing 1 to 5 of 5 for “"Tetralone"”.

  1. Design and synthesis of 3-[N-(cyclopropylmethyl) amino]-7-(methoxy or hydroxy)-2, 2-dimethyl-1-tetralone analogs as potential opioid receptor antagonists

    … )-7 -(hydroxy or methoxy)-2, 2-dimethyl-1-tetralone parent structure. Three synthetic schemes were developed utilizing the common intermediate, ethyl3-benzylamino-2, 2-dimethyl-4-(4- methoxyphenyl)butyrate 3. In Scheme I, compound 3 was modified through a series of six steps to obtain …

    u-pacific Repository record for Design and synthesis of 3-[N-(cyclopropylmethyl) amino]-7-(methoxy or hydroxy)-2, 2-dimethyl-1-tetralone analogs as potential opioid receptor antagonists (opens in a new tab)

  2. α-Formylations with Chiral Chloroiminium Salts

    … α-formylation of α-methyl indanone and α-methyl tetralone using chiral chloroiminium salts derived from (S)-proline. The asymmetric reactions gave enantiomeric excesses of up to 68%.

    east-anglia Repository record for α-Formylations with Chiral Chloroiminium Salts (opens in a new tab)

  3. Neue chirale Triazoliumsalze in der Carben-katalysierten intramolekularen gekreuzten Benzoin-Reaktion

    … benzoin reaction. Different alpha-hydroxy-tetralone, - indanone- and -chromanone-derivatives could be obtained with generation of a quaternary stereogenic center with high enantioselectivities. This alpha-hydroxy-ketones are structural motifs of many bioactive natural products. Thus, …

    aachen Repository record for Neue chirale Triazoliumsalze in der Carben-katalysierten intramolekularen gekreuzten Benzoin-Reaktion (opens in a new tab)

  4. Inhibitors of human cathepsin L and cruzain as therapeutic agents.

    … of benzophenone, propiophenone, α- and β-tetralone, 4-chromanone, and 4-thiochromenone were evaluated as inhibitors of human cathepsin L. While most of the compounds had IC50 values in the range of 0.4 µM or greater, four were very effective inhibitors of cathepsin L: the benzophenone …

    baylor Repository record for Inhibitors of human cathepsin L and cruzain as therapeutic agents. (opens in a new tab)

  5. Isolierung, Strukturaufklärung und Beiträge zur Synthese von Naturstoffen aus tropischen Heilpflanzen sowie Etablierung chiraler On-line-Analytik

    Die Natur eröffnet mit der strukturellen Vielfalt ihrer Sekundärmetaboliten einen nahezu unerschöpflichen Pool in der Leit- und Wirkstoffsuche nach pharmazeutisch wirksamen Substanzen. Insbesondere die Alkaloide zeichnen sich durch ihre biologischen Wirksamkeiten aus. Eine noch junge, sehr …

    wurz-thes Repository record for Isolierung, Strukturaufklärung und Beiträge zur Synthese von Naturstoffen aus tropischen Heilpflanzen sowie Etablierung chiraler On-line-Analytik (opens in a new tab)