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dc.contributor.author박준우-
dc.date.accessioned2016-08-28T11:08:50Z-
dc.date.available2016-08-28T11:08:50Z-
dc.date.issued2001-
dc.identifier.issn0253-2964-
dc.identifier.otherOAK-891-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/218901-
dc.description.abstract1,2-Diketones, camphorquinone and 1-phenyl-1,2-propanedione, are converted to the corresponding α-hydroxyketones in moderate to good yields by TiO2-catalyzed photochemical reactions in deoxygenated alcoholic media. The reduction yield for 1-phenyl-1,2-propanedione is considerably increased by addition of water or triethylamine.-
dc.languageEnglish-
dc.titlePhotochemical reduction of 1,2-diketones in the presence of TiO2-
dc.typeArticle-
dc.relation.issue11-
dc.relation.volume22-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.startpage1213-
dc.relation.lastpage1216-
dc.relation.journaltitleBulletin of the Korean Chemical Society-
dc.identifier.wosidWOS:000172460000011-
dc.identifier.scopusid2-s2.0-0035540612-
dc.author.googlePark J.W.-
dc.author.googleHong M.J.-
dc.author.googlePark K.K.-
dc.contributor.scopusid박준우(35332923800;8141958400)-
dc.date.modifydate20160801100756-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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