Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5289281 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A new series of 13-acetyl-7,12-dihydro-7-ethylbenz[e]naphtho[1,2-b]azepine (4a-d) and 2-aryl-4-hydroxy-2,3,4,5-tetrahydronaphtho[1,2-b]azepine derivatives (6a-d) have been synthesized from N-allyl-N-benzyl substituted α-naphthylamines (1a-d) by utilizing aromatic amino-Claisen rearrangement, intramolecular Friedel-Crafts alkylation and intramolecular dipolar 1,3-cycloaddition nitrone-olefin reactions.
Related Topics
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Authors
Andrés Felipe Yépez, Alirio Palma, Elena Stashenko, Ali Bahsas, Juan M. Amaro-Luis,