Baylis-Hillman acetates in carbocyclic synthesis: A convenient protocol for synthesis of densely substituted indenes

dc.contributor.author	Basavaiah, Deevi
dc.contributor.author	Reddy, Bhavanam Sekhara
dc.contributor.author	Lingam, Harathi
dc.date.accessioned	2022-03-27T09:01:12Z
dc.date.available	2022-03-27T09:01:12Z
dc.date.issued	2013-02-25
dc.description.abstract	A simple and facile strategy for synthesis of densely substituted indenes have been developed from Baylis-Hillman acetates in a two step protocol, that is, (1) via treatment with DABCO and then reaction with alkyl 3-oxobutanoates in the presence of K2CO3 (2) followed by the intramolecular Friedel-Crafts cyclization of the resulting keto-diesters using titanium tetrachloride. © 2013 Elsevier Ltd. All rights reserved.
dc.identifier.citation	Tetrahedron. v.69(8)
dc.identifier.issn	00404020
dc.identifier.uri	10.1016/j.tet.2012.12.069
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040402012019254
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12277
dc.subject	Baylis-Hillman reaction
dc.subject	Chemo selectivity
dc.subject	Friedel-Crafts reaction
dc.subject	Indene derivatives
dc.subject	Keto-diesters
dc.title	Baylis-Hillman acetates in carbocyclic synthesis: A convenient protocol for synthesis of densely substituted indenes
dc.type	Journal. Article
dspace.entity.type

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