Synthesis of substituted maleimide derivatives using the Baylis-Hillman adducts

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Lenin, Dandamudi V.
dc.contributor.author Veeraraghavaiah, Gorre
dc.date.accessioned 2022-03-27T09:01:24Z
dc.date.available 2022-03-27T09:01:24Z
dc.date.issued 2011-10-10
dc.description.abstract The Baylis-Hillman alcohols, 3-ethoxycarbonyl-3-hydroxy-3-aryl(alkyl)-2-methylenepropanenitriles, derived from α-keto esters and acrylonitrile, have been conveniently transformed into 3,4-disubstituted 1Hpyrrole-2,5-dione (maleimide) derivatives on treatment with FeCl 3/RCO 2H in a one-pot operation.
dc.identifier.citation Current Science. v.101(7)
dc.identifier.issn 00113891
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12283
dc.subject α-Keto esters
dc.subject Baylis-Hillman adducts
dc.subject Cyclization
dc.subject Friedel-Crafts reaction
dc.subject Pyrrole-2,5-diones
dc.title Synthesis of substituted maleimide derivatives using the Baylis-Hillman adducts
dc.type Journal. Article
dspace.entity.type
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