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dc.contributor.author류재상-
dc.date.accessioned2016-08-28T12:08:19Z-
dc.date.available2016-08-28T12:08:19Z-
dc.date.issued2010-
dc.identifier.issn0022-3263-
dc.identifier.otherOAK-6618-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220826-
dc.description.abstractNovel 1,3-dialkyl-1,2,3-triazolium ionic liquids were synthesized via click reactions using 1-trimethylsilylacetylene and alkyl azides and were efficient reaction media for the Baylis-Hillman reaction. The problems associated with deprotonation of the C-2 hydrogen of [bmim][PF6] could be suppressed in the reaction of [bmTr][PF6] or [bmTr][NTf2]. 1,3-Dialkyl-1,2,3-triazolium ionic liquids are chemically inert under basic conditions and more suitable media for the reactions involving bases than the common 1,3-dialkylimidazolium ionic liquids. © 2010 American Chemical Society.-
dc.languageEnglish-
dc.titleSynthesis of 1,3-Dialkyl-1,2,3-triazolium ionic liquids and their applications to the baylis-hillman reaction-
dc.typeArticle-
dc.relation.issue12-
dc.relation.volume75-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage4183-
dc.relation.lastpage4191-
dc.relation.journaltitleJournal of Organic Chemistry-
dc.identifier.doi10.1021/jo100618d-
dc.identifier.wosidWOS:000278560700026-
dc.identifier.scopusid2-s2.0-77953507131-
dc.author.googleJeong Y.-
dc.author.googleRyu J.-S.-
dc.contributor.scopusid류재상(36081118200)-
dc.date.modifydate20170601153005-
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약학대학 > 약학과 > Journal papers
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