Abstract
The first three-component coupling reactions between various anilines (1), benzaldehydes (2), and cyclohexen- 2-one (3) were performed under mild conditions (acetonitrile, room temperature, 14 h) in the presence of 20 mol % BiCl3 to obtain new 2,3-diaryl-2-aza[2.2.2]octan-5-ones (4,5) with interesting acetylcholinesterase inhibitory properties.
Keywords: 2,3-Diaryl-2-azabicyclo[2.2.2]octan-5-one, catalysed three-component aza Diels-Alder reaction, acetylcholinesterase inhibitors
Letters in Organic Chemistry
Title: An Efficient Synthesis of 2,3-Diaryl-2-azabicyclooctanones Via BiCl3- Catalysed Three-Component aza Diels-Alder Reaction
Volume: 5 Issue: 7
Author(s): Luis Astudillo S., Gabriel A. Vallejos, Nestor Correa, Margarita Gutierrez C., Walesca de la Guarda and Vladimir V. Kouznetsov
Affiliation:
Keywords: 2,3-Diaryl-2-azabicyclo[2.2.2]octan-5-one, catalysed three-component aza Diels-Alder reaction, acetylcholinesterase inhibitors
Abstract: The first three-component coupling reactions between various anilines (1), benzaldehydes (2), and cyclohexen- 2-one (3) were performed under mild conditions (acetonitrile, room temperature, 14 h) in the presence of 20 mol % BiCl3 to obtain new 2,3-diaryl-2-aza[2.2.2]octan-5-ones (4,5) with interesting acetylcholinesterase inhibitory properties.
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Cite this article as:
S. Astudillo Luis, Vallejos A. Gabriel, Correa Nestor, C. Gutierrez Margarita, de la Guarda Walesca and Kouznetsov V. Vladimir, An Efficient Synthesis of 2,3-Diaryl-2-azabicyclooctanones Via BiCl3- Catalysed Three-Component aza Diels-Alder Reaction, Letters in Organic Chemistry 2008; 5 (7) . https://dx.doi.org/10.2174/157017808785982301
DOI https://dx.doi.org/10.2174/157017808785982301 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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