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FeCl3·6H2O-catalyzed Intramolecular Allylic Amination: Synthesis of Substituted Dihydroquinolines and Quinolines

Overview
Journal J Org Chem
Specialty Chemistry
Date 2012 Sep 1
PMID 22934926
Citations 4
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Abstract

A facile and efficient method to synthesize 2- or 4-substituted 1,2-dihydroquinolines and quinolines catalyzed by FeCl(3)·6H(2)O (2 mol %) was described. The iron-catalyzed intramolecular allylic amination of 2-aminophenyl-1-en-3-ols proceeded smoothly to afford 13 1,2-dihydroquinoline and 8 quinoline derivatives under mild reaction conditions with good to excellent yields (up to 96%).

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