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

dc.contributor.author	Basavaiah, Deevi
dc.contributor.author	Lenin, Dandamudi V.
dc.date.accessioned	2022-03-27T09:01:26Z
dc.date.available	2022-03-27T09:01:26Z
dc.date.issued	2010-10-01
dc.description.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.
dc.identifier.citation	European Journal of Organic Chemistry
dc.identifier.issn	1434193X
dc.identifier.uri	10.1002/ejoc.201000739
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/ejoc.201000739
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12284
dc.subject	Alkylation
dc.subject	Baylis-Hillman reaction
dc.subject	Carbocycles
dc.subject	Cyclization
dc.subject	Synthetic methods
dc.title	A facile synthesis of substituted indenones and piperidine-2,6-diones from the baylis-hillman acetates
dc.type	Journal. Article
dspace.entity.type

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