A novel tandem process leading to functionalized glutarimides

dc.creator	Popović-Djordjević, Jelena
dc.creator	Ivanović, MD
dc.creator	Kiricojević, Vesna D.
dc.date.accessioned	2020-12-17T18:33:04Z
dc.date.available	2020-12-17T18:33:04Z
dc.date.issued	2005
dc.identifier.issn	0040-4039
dc.identifier.uri	http://aspace.agrif.bg.ac.rs/handle/123456789/1022
dc.description.abstract	The synthesis of various functionalized or spirobicyclic glutarimides by a novel tandem process has been disclosed. The reaction involves a base-catalyzed Michael addition of active methylene compounds to secondary conjugated amides, followed by intramolecular N-acylation of the carboxamido group. It provides a relatively general and simple access to useful synthetic intermediaries and potentially active pharmacological compounds. In addition, a novel group of spirobicyclic systems has been synthesized.	en
dc.publisher	Pergamon-Elsevier Science Ltd, Oxford
dc.rights	restrictedAccess
dc.source	Tetrahedron Letters
dc.subject	synthesis	en
dc.subject	functionalized or spirobicyclic glutarimides	en
dc.subject	tandem process	en
dc.title	A novel tandem process leading to functionalized glutarimides	en
dc.type	article
dc.rights.license	ARR
dc.citation.epage	2614
dc.citation.issue	15
dc.citation.other	46(15): 2611-2614
dc.citation.rank	M22
dc.citation.spage	2611
dc.citation.volume	46
dc.identifier.doi	10.1016/j.tetlet.2005.02.087
dc.identifier.scopus	2-s2.0-15244347524
dc.identifier.wos	000228115600019
dc.type.version	publishedVersion