Abstract
A number of α,β-unsaturated carboxylic acids were reacted with electron rich arenes or heteroarene in the presence of trifluoroacetic anhydride (TFAA) and H3PO4 at room temperature to give a variety of chalcone derivatives in good to excellent yields. The methodology was used to prepare novel compounds of potential pharmacological significances.
Keywords: Chalcones, TFAA, α, β-unsaturated carboxylic acids, arenes
Letters in Organic Chemistry
Title: A New and Direct Synthesis of Chalcones Via TFAA-H3PO4 Mediated C-C Bond Forming Reaction
Volume: 8 Issue: 1
Author(s): Kavitha Kankanala, Lingam Venkata Reddy, Vangala Ranga Reddy, Khagga Mukkanti and Sarbani Pal
Affiliation:
Keywords: Chalcones, TFAA, α, β-unsaturated carboxylic acids, arenes
Abstract: A number of α,β-unsaturated carboxylic acids were reacted with electron rich arenes or heteroarene in the presence of trifluoroacetic anhydride (TFAA) and H3PO4 at room temperature to give a variety of chalcone derivatives in good to excellent yields. The methodology was used to prepare novel compounds of potential pharmacological significances.
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Cite this article as:
Kankanala Kavitha, Venkata Reddy Lingam, Ranga Reddy Vangala, Mukkanti Khagga and Pal Sarbani, A New and Direct Synthesis of Chalcones Via TFAA-H3PO4 Mediated C-C Bond Forming Reaction, Letters in Organic Chemistry 2011; 8 (1) . https://dx.doi.org/10.2174/157017811794557750
DOI https://dx.doi.org/10.2174/157017811794557750 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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