A facile synthesis of substituted indenones and piperidine-2,6-diones from the baylis-hillman acetates
A facile synthesis of substituted indenones and piperidine-2,6-diones from the baylis-hillman acetates
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Date
2010-10-01
Authors
Basavaiah, Deevi
Lenin, Dandamudi V.
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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. 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. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Description
Keywords
Alkylation,
Baylis-Hillman reaction,
Carbocycles,
Cyclization,
Synthetic methods
Citation
European Journal of Organic Chemistry