Simple and facile synthesis of tetralone-spiro-glutarimides and spiro-bisglutarimides from Baylis-Hillman acetates

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Reddy, Raju Jannapu
dc.date.accessioned 2022-03-27T09:01:48Z
dc.date.available 2022-03-27T09:01:48Z
dc.date.issued 2008-08-14
dc.description.abstract A simple and convenient synthesis of di(E)-arylidene-tetralone-spiro- glutarimides from Baylis-Hillman acetates via an interesting biscyclization strategy involving facile C-C and C-N bond formation is described. Also, one-pot multistep transformation of the Baylis-Hillman acetates into di(E)-arylidene-spiro-bisglutarimides is presented. © 2008 The Royal Society of Chemistry.
dc.identifier.citation Organic and Biomolecular Chemistry. v.6(6)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/b717843c
dc.identifier.uri http://xlink.rsc.org/?DOI=b717843c
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12295
dc.title Simple and facile synthesis of tetralone-spiro-glutarimides and spiro-bisglutarimides from Baylis-Hillman acetates
dc.type Journal. Article
dspace.entity.type
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