Abstract
Poly-substituted quinolines are readily prepared in excellent yields via a Friedlander reaction of oaminoarylketone or o-aminoarylaldehyde with α-methylene ketones in the presence of BiCl3 under solventfree and thermal heating conditions.
Keywords: solvent-free., BiCl3, Friedländer reaction, α-methylene ketones, o-aminoaryl ketones, Quinoline
Letters in Organic Chemistry
Title: Efficient Solvent-Free Synthesis of Quinolines Promoted by BiCl3
Volume: 3 Issue: 4
Author(s): Guan-Wu Wang and Cheng-Sheng Jia
Affiliation:
Keywords: solvent-free., BiCl3, Friedländer reaction, α-methylene ketones, o-aminoaryl ketones, Quinoline
Abstract: Poly-substituted quinolines are readily prepared in excellent yields via a Friedlander reaction of oaminoarylketone or o-aminoarylaldehyde with α-methylene ketones in the presence of BiCl3 under solventfree and thermal heating conditions.
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Cite this article as:
Wang Guan-Wu and Jia Cheng-Sheng, Efficient Solvent-Free Synthesis of Quinolines Promoted by BiCl3, Letters in Organic Chemistry 2006; 3 (4) . https://dx.doi.org/10.2174/157017806776114568
DOI https://dx.doi.org/10.2174/157017806776114568 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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