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Synthesis 2008(11): 1737-1740
DOI: 10.1055/s-2008-1067039
DOI: 10.1055/s-2008-1067039
PAPER
© Georg Thieme Verlag Stuttgart · New York
Tris(pentafluorophenyl)borane-Catalyzed Three-Component Reaction for the Synthesis of 1,8-Dioxodecahydroacridines under Solvent-Free Conditions
Further Information
Received
8 January 2008
Publication Date:
29 April 2008 (online)
Publication History
Publication Date:
29 April 2008 (online)

Abstract
A mild and efficient method for the synthesis of 1,8-dioxodecahydroacridines has been developed. The synthesis proceeds via a three-component reaction of a 1,3-dione, an aldehyde and an amine, under solvent-free conditions, catalyzed by tris(pentafluorophenyl)borane [B(C6F5)3]. The mildness of the catalyst was demonstrated by studying the reaction of 1,3-cyclohexanedione with various aldehydes and amines which gave the 1,8-dioxodecahydroacridines in high yields.
Key words
Hantzsch reaction - acridinediones - tris(pentafluorophenyl)borane - three-component reaction - Lewis acid
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