Tris(pentafluorophenyl)borane-catalyzed three-component reaction for the synthesis of 1,8-dioxodecahydroacridines under solvent-free conditions

dc.contributor.author	Chandrasekhar, Srivari
dc.contributor.author	Rao, Yaragorla Srinivasa
dc.contributor.author	Sreelakshmi, Leila
dc.contributor.author	Mahipal, Bodugam
dc.contributor.author	Reddy, Chada Raji
dc.date.accessioned	2022-03-27T08:50:24Z
dc.date.available	2022-03-27T08:50:24Z
dc.date.issued	2008-06-02
dc.description.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(C 6F5)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-dioxo-decahydroacridines in high yields.
dc.identifier.citation	Synthesis
dc.identifier.issn	00397881
dc.identifier.uri	10.1055/s-2008-1067039
dc.identifier.uri	http://www.thieme-connect.de/DOI/DOI?10.1055/s-2008-1067039
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/11911
dc.subject	Acridinediones
dc.subject	Hantzsch reaction
dc.subject	Lewis acid
dc.subject	Three-component reaction
dc.subject	Tris(pentafluorophenyl)borane
dc.title	Tris(pentafluorophenyl)borane-catalyzed three-component reaction for the synthesis of 1,8-dioxodecahydroacridines under solvent-free conditions
dc.type	Journal. Article
dspace.entity.type

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