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dc.contributor.authorShunichi Fukuzumi*
dc.date.accessioned2016-08-28T10:08:09Z-
dc.date.available2016-08-28T10:08:09Z-
dc.date.issued2012*
dc.identifier.issn2046-2069*
dc.identifier.otherOAK-9542*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/223254-
dc.description.abstractThe hydroxyl radical-scavenging activity of the amino-substituted α-tocopherol analogues was much higher than that of α-tocopherol. Aminochromanoxyl radicals generated from 5- and 7-aminochromanol were successfully detected in aqueous solution at room temperature during ESR measurements. The stability of the aminochromanoxyl radicals leads to a significant enhancement of the radical-scavenging activity. © 2012 The Royal Society of Chemistry.*
dc.languageEnglish*
dc.titleThe high stability of intermediate radicals enhances the radical-scavenging activity of aminochromanols*
dc.typeArticle*
dc.relation.issue33*
dc.relation.volume2*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage12714*
dc.relation.lastpage12717*
dc.relation.journaltitleRSC Advances*
dc.identifier.doi10.1039/c2ra21928j*
dc.identifier.wosidWOS:000312149600028*
dc.identifier.scopusid2-s2.0-84870051024*
dc.author.googleInami K.*
dc.author.googleNakanishi I.*
dc.author.googleMorita M.*
dc.author.googleFurukawa M.*
dc.author.googleOhkubo K.*
dc.author.googleFukuzumi S.*
dc.author.googleMochizuki M.*
dc.contributor.scopusidShunichi Fukuzumi(35430038100;58409757400)*
dc.date.modifydate20240401081001*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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