Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5269893 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Stereochemical and synthetic aspects encountered during the preparation of the four possible isomers of 1 are reported. The 5-aryl 2-azabicyclo [3.2.1] octane derivatives represent a novel class of compounds which can be deemed as an example of aryl-piperidine conformationally constrained of potential interest for medicinal chemistry exploration. In particular isomers of 1 are characterised by a potent in vitro serotonine, dopamine and noradrenaline re-uptake inhibitor (TRUI) activity superior/comparable to standard compounds such as DOV 21,947 and DOV 102,677.
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Authors
Roberto Profeta, Jens Klein, Simone Spada, Francesco Ferroni, Alfredo Paio, Daniele Andreotti,