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dc.contributor.author김원석*
dc.date.accessioned2016-08-27T04:08:13Z-
dc.date.available2016-08-27T04:08:13Z-
dc.date.issued2015*
dc.identifier.issn2046-2069*
dc.identifier.otherOAK-15706*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/217652-
dc.description.abstractAn efficient method for the synthesis of ketones using organolithium and acid chlorides under continuous flow conditions has been developed. In contrast to standard batch chemistry, over-addition of the organolithium to the ketone for the formation of the undesired tertiary alcohol has been minimised representing a direct approach toward ketones.*
dc.languageEnglish*
dc.publisherROYAL SOC CHEMISTRY*
dc.titleSynthesis of ketones via organolithium addition to acid chlorides using continuous flow chemistry*
dc.typeArticle*
dc.relation.issue97*
dc.relation.volume5*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage79385*
dc.relation.lastpage79390*
dc.relation.journaltitleRSC ADVANCES*
dc.identifier.doi10.1039/c5ra14890a*
dc.identifier.wosidWOS:000361834900018*
dc.identifier.scopusid2-s2.0-84942465899*
dc.author.googleMoon, Soo-Yeon*
dc.author.googleJung, Seo-Hee*
dc.author.googleBin Kim, U.*
dc.author.googleKim, Won-Suk*
dc.contributor.scopusid김원석(57203484044)*
dc.date.modifydate20240220102223*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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