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  5. A simple and efficient method for the synthesis of Erlenmeyer azlactones
 
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A simple and efficient method for the synthesis of Erlenmeyer azlactones

Author(s)
Conway, Philip A.  
Devine, Kevin  
Paradisi, Francesca  
Uri
http://hdl.handle.net/10197/3637
Date Issued
2009-04-11
Date Available
2012-06-13T13:57:31Z
Abstract
We have recently developed a novel and efficient method for synthesising Erlenmeyer azlactones under mild and rapid conditions. The reaction is performed by reacting 2-phenyl-5-oxazolone with an aldehyde in dichloromethane using alumina as a catalyst. The materials react instantly at room temperature, negating the need for high temperatures and long reaction times. We have successfully used this method for both aliphatic, aromatic and heteroaromatic aldehydes, synthesising previously unmade Erlenmeyer azlactones in moderate to high yields.
Sponsorship
Science Foundation Ireland
Type of Material
Journal Article
Publisher
Elsevier
Journal
Tetrahedron
Volume
65
Issue
15
Start Page
2935
End Page
2938
Copyright (Published Version)
2009 Elsevier
Subjects

Aromatic azlactones

Aliphatic azlactones

solid-phase catalysis...

Subject – LCSH
Aromatic compounds
Aliphatic compounds
Solid-phase synthesis
DOI
10.1016/j.tet.2009.02.011
Language
English
Status of Item
Peer reviewed
This item is made available under a Creative Commons License
https://creativecommons.org/licenses/by-nc-sa/1.0/
File(s)
No Thumbnail Available
Name

Conway Tetrahdron 2009.doc

Size

188 KB

Format

Microsoft Word

Checksum (MD5)

b0b8cd7f0ca513e030115e0f0e768f2a

Owning collection
Chemistry Research Collection

Item descriptive metadata is released under a CC-0 (public domain) license: https://creativecommons.org/public-domain/cc0/.
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