A facile synthesis of substituted indenones and piperidine-2,6-diones from the Baylis-Hillman acetates

Basavaiah, Deevi ; Lenin, Dandamudi V. (2010) A facile synthesis of substituted indenones and piperidine-2,6-diones from the Baylis-Hillman acetates European Journal of Organic Chemistry, 2010 (29). pp. 5650-5658. ISSN 1434-193X

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/ejoc.20...

Related URL: http://dx.doi.org/10.1002/ejoc.201000739

Abstract

Baylis-Hillman acetates were conveniently transformed into substituted indenone and piperidine-2,6-dione frameworks by treatment with (di)phenylacetonitrile followed by Friedel-Crafts cyclization or imide formation.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Alkylation; Carbocycles; Cyclization; Baylis-Hillman Reaction; Synthetic Methods
ID Code:85761
Deposited On:06 Mar 2012 04:45
Last Modified:06 Mar 2012 04:45

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