An expeditious approach to quinolines via Friedländer synthesis catalyzed by FeCl3 or Mg(ClO4)2

Jie Wu; Liang Zhang; Tian Ning Diao

doi:10.1055/s-2005-917111

An expeditious approach to quinolines via Friedländer synthesis catalyzed by FeCl₃ or Mg(ClO₄)₂

Jie Wu, Liang Zhang, Tian Ning Diao

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

A mild and efficient route for the synthesis of quinolines and polycyclic quinolines utilizing FeCl₃ or Mg(ClO₄)₂ as a novel catalyst via Friedländer annulation was described.

Original language	English (US)
Article number	W01605ST
Pages (from-to)	2653-2657
Number of pages	5
Journal	Synlett
Issue number	17
DOIs	https://doi.org/10.1055/s-2005-917111
State	Published - Oct 17 2005

Keywords

Catalyst
FeCl
Friedländer synthesis
Mg(ClO )
Quinoline

ASJC Scopus subject areas

Organic Chemistry

Access to Document

10.1055/s-2005-917111

Cite this

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title = "An expeditious approach to quinolines via Friedl{\"a}nder synthesis catalyzed by FeCl3 or Mg(ClO4)2",

abstract = "A mild and efficient route for the synthesis of quinolines and polycyclic quinolines utilizing FeCl3 or Mg(ClO4)2 as a novel catalyst via Friedl{\"a}nder annulation was described.",

keywords = "Catalyst, FeCl, Friedl{\"a}nder synthesis, Mg(ClO ), Quinoline",

author = "Jie Wu and Liang Zhang and Diao, {Tian Ning}",

year = "2005",

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