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pubmed-article:21694667pubmed:abstractTextLithium diphenylbinaphtholate catalyzed the enantioselective Evans-Tishchenko reduction of achiral ?-hydroxyketones to afford monoacyl-protected 1,3-diols with high stereoselectivities. In the reaction of racemic ?-hydroxyketones, kinetic optical resolution occurred in a highly stereoselective manner.lld:pubmed
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pubmed-article:21694667pubmed:articleTitleEnantioselective Evans-Tishchenko reduction of ?-hydroxyketone catalyzed by lithium binaphtholate.lld:pubmed
pubmed-article:21694667pubmed:affiliationGraduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan.lld:pubmed
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