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A novel tandem process leading to functionalized glutarimides
| dc.creator | Popović-Đorđević, Jelena B. | |
| dc.creator | Ivanović, Milovan D. | |
| dc.creator | Kiricojević, Vesna | |
| dc.date.accessioned | 2019-04-24T14:52:05Z | |
| dc.date.available | 2019-04-24T14:52:05Z | |
| dc.date.issued | 2005 | |
| dc.identifier.issn | 0040-4039 | |
| dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/2678 | |
| 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. (c) 2005 Elsevier Ltd. All rights reserved. | en |
| dc.publisher | Oxford : Pergamon-Elsevier Science Ltd | |
| 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 | |
| dcterms.abstract | Поповић-Ђорђевић, Јелена Б.; Ивановић, Милован; Кирицојевиц, В. Д.; | |
| dc.citation.volume | 46 | |
| dc.citation.issue | 15 | |
| dc.citation.spage | 2611 | |
| dc.citation.epage | 2614 | |
| dc.citation.other | 46(15): 2611-2614 | |
| dc.citation.rank | M22 | |
| 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 | en |
