Title of article :
2-Allyl-N-benzyl substituted α-naphthylamines as building blocks in heterocyclic synthesis. New and efficient syntheses of benz[e]naphtho[1,2-b]azepine and naphtho[1,2-b]azepine derivatives
Author/Authors :
Yépez، نويسنده , , Andrés Felipe and Palma، نويسنده , , Alirio and Stashenko، نويسنده , , Elena and Bahsas، نويسنده , , Ali and Amaro-Luis، نويسنده , , Juan M.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2006
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.
Keywords :
2-b]azepines , 3-Cycloaddition , Intramolecular Friedel–Crafts alkylation , 2-b]azepines , Intramolecular dipolar 1 , Amino-Claisen rearrangement
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters