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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 44, 2014 - Issue 5
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Original Articles

Expeditious Synthesis of Aromatic Cyanodienones Using Neutral Alumina as a Versatile Heterogeneous Catalyst

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Pages 640-647 | Received 15 Jun 2013, Published online: 27 Dec 2013
 

Abstract

The work described herein employs neutral alumina as an effective catalyst for ring opening of triarylpyrylium perchlorates to corresponding aromatic cyanodienones, which have main roles in biological activities. The present porous catalyst has several advantages, it is inexpensive, thermally and mechanically stable, nontoxic, and highly resistant against organic solvents. It increases the reaction rate many fold when compared with conventional reaction conditions. Moreover, the recovered alumina can be used several times without serious decrease in activity.

[Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.]

GRAPHICAL ABSTRACT

ACKNOWLEDGMENT

This work was supported by the Research Council at the University of Shahid Chamran.

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