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Reactions of ortho-substituted alpha,alpha-dibromoacetophenones with nucleophiles: first examples of combined carbophilic and bromophilic attack on C-Br bonds
dc.creator | Tatar, Jovana | |
dc.creator | Baranac-Stojanović, Marija | |
dc.creator | Stojanović, Milovan | |
dc.creator | Marković, Rade | |
dc.date.accessioned | 2018-11-22T00:14:09Z | |
dc.date.available | 2018-11-22T00:14:09Z | |
dc.date.issued | 2009 | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.uri | https://cherry.chem.bg.ac.rs/handle/123456789/606 | |
dc.description.abstract | An efficient method for the formation of alpha-carbonyl-monosubstituted acetophenones from ortho-methoxy-and ortho-hydroxy-alpha,alpha-dibromoacetopheiiones and a range of selected nucleophiles, occurring via a carbophilic substitution/bromophilic substitution/protonation cascade process, is described. In turn, the preparation of alpha,alpha-dibromoacetophenones, isolated in high yields, relies on the neighboring group participation of the ortho-substituents in the starting ortho-substituted acetophenones. (C) 2008 Elsevier Ltd. All rights reserved | en |
dc.publisher | Pergamon-Elsevier Science Ltd, Oxford | |
dc.relation | info:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS// | |
dc.rights | restrictedAccess | |
dc.source | Tetrahedron Letters | |
dc.title | Reactions of ortho-substituted alpha,alpha-dibromoacetophenones with nucleophiles: first examples of combined carbophilic and bromophilic attack on C-Br bonds | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Баранац-Стојановић, Марија; Марковиц, Раде; Стојановиц, Милован; Татар, Јована; | |
dc.citation.volume | 50 | |
dc.citation.issue | 6 | |
dc.citation.spage | 700 | |
dc.citation.epage | 703 | |
dc.identifier.wos | 000263310800025 | |
dc.identifier.doi | 10.1016/j.tetlet.2008.11.104 | |
dc.citation.other | 50(6): 700-703 | |
dc.citation.rank | M22 | |
dc.type.version | publishedVersion | en |
dc.identifier.scopus | 2-s2.0-57749201586 |