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dc.creatorPopović-Đorđević, Jelena B.
dc.creatorIvanović, Milovan D.
dc.creatorKiricojević, Vesna
dc.date.accessioned2019-04-24T14:52:05Z
dc.date.available2019-04-24T14:52:05Z
dc.date.issued2005
dc.identifier.issn0040-4039
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2678
dc.description.abstractThe 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. (c) 2005 Elsevier Ltd. All rights reserved.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.rightsrestrictedAccess
dc.sourceTetrahedron Letters
dc.subjectsynthesisen
dc.subjectfunctionalized or spirobicyclic glutarimidesen
dc.subjecttandem processen
dc.titleA novel tandem process leading to functionalized glutarimidesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractПоповић-Ђорђевић, Јелена Б.; Ивановић, Милован; Кирицојевиц, В. Д.;
dc.citation.volume46
dc.citation.issue15
dc.citation.spage2611
dc.citation.epage2614
dc.citation.other46(15): 2611-2614
dc.citation.rankM22
dc.identifier.doi10.1016/j.tetlet.2005.02.087
dc.identifier.scopus2-s2.0-15244347524
dc.identifier.wos000228115600019
dc.type.versionpublishedVersionen


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