Baylis-Hillman carbonates in organic synthesis: A convenient one-pot strategy for nitrone-spiro-oxindole frameworks

dc.contributor.author	Basavaiah, Deevi
dc.contributor.author	Badsara, Satpal Singh
dc.contributor.author	Veeraraghavaiah, Gorre
dc.date.accessioned	2022-03-27T09:01:06Z
dc.date.available	2022-03-27T09:01:06Z
dc.date.issued	2013-09-16
dc.description.abstract	A facile one-pot protocol for synthesis of nitrone-spiro-oxindole frameworks via alkylation of nitromethane with carbonates of Baylis-Hillman alcohols, derived from isatins and cyclohex-2-enone derivatives, followed by reductive cyclization is described. © 2013 Elsevier Ltd. All rights reserved.
dc.identifier.citation	Tetrahedron. v.69(37)
dc.identifier.issn	00404020
dc.identifier.uri	10.1016/j.tet.2013.07.002
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040402013010685
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12274
dc.subject	Alkylation
dc.subject	Baylis-Hillman reaction
dc.subject	Nitrones
dc.subject	Reductive cyclization
dc.subject	Spiro-oxindoles
dc.title	Baylis-Hillman carbonates in organic synthesis: A convenient one-pot strategy for nitrone-spiro-oxindole frameworks
dc.type	Journal. Article
dspace.entity.type

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