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dc.creatorTatar, Jovana
dc.creatorMarković, Rade
dc.creatorStojanović, Milovan
dc.creatorBaranac-Stojanović, Marija
dc.date.accessioned2019-01-30T17:23:58Z
dc.date.available2019-01-30T17:23:58Z
dc.date.issued2010
dc.identifier.issn0040-4039
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/703
dc.description.abstractalpha,alpha-Dibromo-2-methoxyacetophenone reacts, under mild reaction conditions, with C-, N- and O-nucleophiles via a bromophilic substitution/protonation/carbophilic substitution cascade process to afford alpha-monosubstituted-2-methoxyacetophenones in moderate to good yield. The only exception from this reaction pathway is the reaction with the anion derived from malononitrile in which 2-aroyl-1,1,3,3-tetracyanopropene is obtained.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS//
dc.rightsrestrictedAccess
dc.sourceTetrahedron Letters
dc.subjectalpha,alpha-Dibromomethylketoneen
dc.subjectBromophilic reactionen
dc.subjectNucleophilic substitutionen
dc.subjectCascade reactionsen
dc.titleBromophilic substitution/carbophilic substitution cascade reactions of alpha,alpha-dibromo-2-methoxyacetophenone with C-, N- and O-nucleophilesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМарковиц, Раде; Татар, Јована; Баранац-Стојановиц, Марија; Стојановић, Милован;
dc.citation.volume51
dc.citation.issue37
dc.citation.spage4851
dc.citation.epage4855
dc.citation.other51(37): 4851-4855
dc.citation.rankM22
dc.identifier.doi10.1016/j.tetlet.2010.07.057
dc.identifier.rcubConv_2541
dc.identifier.scopus2-s2.0-77955848118
dc.identifier.wos000281356700017
dc.type.versionpublishedVersion


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