Less reactive ketones as electrophiles and acrylamides as activated alkenes in intramolecular Baylis-Hillman reaction: Facile synthesis of functionalized γ-lactam frameworks

dc.contributor.author	Basavaiah, Deevi
dc.contributor.author	Reddy, Guddeti Chandrashekar
dc.contributor.author	Bharadwaj, Kishor Chandra
dc.date.accessioned	2022-03-27T09:00:55Z
dc.date.available	2022-03-27T09:00:55Z
dc.date.issued	2014-10-28
dc.description.abstract	Less reactive ketones and acrylamides have been successfully employed as electrophiles and activated alkenes, respectively, in intramolecular Baylis-Hillman reaction, thus providing a facile protocol for obtaining functionalized α-methylene-γ-lactam derivatives.
dc.identifier.citation	Tetrahedron. v.70(43)
dc.identifier.issn	00404020
dc.identifier.uri	10.1016/j.tet.2014.08.045
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040402014012290
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12268
dc.subject	Acrylamide ketones
dc.subject	Baylis-Hillman reaction
dc.subject	DABCO
dc.subject	Lactam
dc.subject	Nitrogen heterocycles
dc.title	Less reactive ketones as electrophiles and acrylamides as activated alkenes in intramolecular Baylis-Hillman reaction: Facile synthesis of functionalized γ-lactam frameworks
dc.type	Journal. Article
dspace.entity.type

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