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Synthesis 2010(5): 803-806
DOI: 10.1055/s-0029-1218584
DOI: 10.1055/s-0029-1218584
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
An Efficient, One-Pot, Multicomponent Synthesis of β-Acetamido Carbonyl Compounds Using Cyanuric Chloride in an Aqueous Medium [¹]
Further Information
Received
19 October 2009
Publication Date:
07 December 2009 (online)
Publication History
Publication Date:
07 December 2009 (online)
Abstract
A one-pot, three-component reaction between an aromatic aldehyde, an enolizable ketone or a β-keto ester, and a nitrile in the presence of acetyl chloride is accomplished efficiently using cyanuric chloride in an aqueous medium to give the corresponding β-acetamido ketone or ester in high yield.
Key words
β-acetamido ketone - multicomponent reaction - cyanuric chloride - aqueous medium
Part 198 in the series ‘Studies on novel synthetic methodologies’.
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Part 198 in the series ‘Studies on novel synthetic methodologies’.