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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;7405812170)-
dc.date.modifydate20220119154254-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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