FIRST ENANTIOSELECTIVE SYNTHESIS OF TETRAHYDROCHROMENO[2,3-<i>b</i>]CARBAZOLYLACETALDEHYDE <i>VIA</i> TRIENAMINE CATALYSIS AND ITS BIOLOGICAL ACTIVITY
DOI:
https://doi.org/10.1007/6495Keywords:
tetrahydrochromeno[2, 3-b]carbazole, anxiolytic activity, enantioselective synthesis, organocatalysis, trienamine catalysisAbstract
The first enantioselective synthesis of a tetrahydrochromeno[2,3-b]carbazole derivative via trienamine catalysis is presented. This molecule reduced the anxiety-like behavior in mice. On the contrary, its enantiomer showed low activity, demonstrating the importance of the stereochemisty in the corresponding cycloadduct. On the other hand, both enantiomers showed low antidepressant-like activity.Downloads
Published
2022-07-21
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Short Communications