Baylis-Hillman acetates in organic synthesis: A simple two-step strategy for oxindole-spiro-α-arylidene-γ-butyrolactone framework

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Lingam, Harathi
dc.contributor.author Babu, Thelagathoti Hari
dc.date.accessioned 2022-03-27T09:00:41Z
dc.date.available 2022-03-27T09:00:41Z
dc.date.issued 2018-05-10
dc.description.abstract A facile, convenient, and two step strategy for synthesis of spirooxindoles containing α-arylidene-γ-butyrolactone moiety has been developed via monoalkylation of 2-oxindoles with Baylis-Hillman acetates followed by the spirolactonization of the resulting cinnamic esters on treatment with phenyliodine (III) bistrifluoroacetate (PIFA).
dc.identifier.citation Tetrahedron. v.74(19)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/j.tet.2018.03.035
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040402018302783
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12261
dc.subject Baylis-Hillman reaction
dc.subject PIFA
dc.subject Spirolactonization
dc.subject Spirooxindole
dc.subject γ-Butyrolactone
dc.title Baylis-Hillman acetates in organic synthesis: A simple two-step strategy for oxindole-spiro-α-arylidene-γ-butyrolactone framework
dc.type Journal. Article
dspace.entity.type
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