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Cited 54 time in webofscience Cited 62 time in scopus
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dc.contributor.authorKim, MJ-
dc.contributor.authorChoi, YK-
dc.contributor.authorKim, S-
dc.contributor.authorKim, D-
dc.contributor.authorHan, K-
dc.contributor.authorKo, SB-
dc.contributor.authorPark, J-
dc.date.accessioned2016-04-01T01:24:38Z-
dc.date.available2016-04-01T01:24:38Z-
dc.date.created2009-02-28-
dc.date.issued2008-03-20-
dc.identifier.issn1523-7060-
dc.identifier.other2008-OAK-0000007599-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/22867-
dc.description.abstractA practical procedure has been developed for the dynamic kinetic resolution of 1,2-diarylethanols. This procedure employs a highly enantioselective lipase from Pseudomonas stutzeri (trade name, lipase TL) as the resolution catalyst and a ruthenium complex as the racemization catalyst. Sixteen 1,2-diarylethanols have been efficiently resolved to provide their acetyl derivatives with good yields (95-97%) and high enantiomeric excesses (96-99%).-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfORGANIC LETTERS-
dc.subjectMETAL COMBO CATALYSIS-
dc.subjectSECONDARY ALCOHOLS-
dc.subjectRACEMIZATION CATALYSTS-
dc.subjectAMBIENT-TEMPERATURE-
dc.subjectASYMMETRIC TRANSFORMATIONS-
dc.subjectENZYMATIC RESOLUTION-
dc.subjectALLYLIC ALCOHOLS-
dc.subjectENANTIOMERS-
dc.subjectENZYMES-
dc.subjectCOMBINATION-
dc.titleHighly enantioselective dynamic kinetic resolution of 1,2-diarylethanols by a lipase-ruthenium couple-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1021/OL800163Z-
dc.author.googleKim, MJ-
dc.author.googleChoi, YK-
dc.author.googleKim, S-
dc.author.googleKim, D-
dc.author.googleHan, K-
dc.author.googleKo, SB-
dc.author.googlePark, J-
dc.relation.volume10-
dc.relation.issue6-
dc.relation.startpage1295-
dc.relation.lastpage1298-
dc.contributor.id10075891-
dc.relation.journalORGANIC LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.10, no.6, pp.1295 - 1298-
dc.identifier.wosid000254032100065-
dc.date.tcdate2019-01-01-
dc.citation.endPage1298-
dc.citation.number6-
dc.citation.startPage1295-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume10-
dc.contributor.affiliatedAuthorKim, MJ-
dc.contributor.affiliatedAuthorPark, J-
dc.identifier.scopusid2-s2.0-45549107870-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc44-
dc.description.scptc51*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusMETAL COMBO CATALYSIS-
dc.subject.keywordPlusSECONDARY ALCOHOLS-
dc.subject.keywordPlusRACEMIZATION CATALYSTS-
dc.subject.keywordPlusAMBIENT-TEMPERATURE-
dc.subject.keywordPlusASYMMETRIC TRANSFORMATIONS-
dc.subject.keywordPlusENZYMATIC RESOLUTION-
dc.subject.keywordPlusALLYLIC ALCOHOLS-
dc.subject.keywordPlusENANTIOMERS-
dc.subject.keywordPlusENZYMES-
dc.subject.keywordPlusCOMBINATION-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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김만주KIM, MAHN JOO
Dept of Chemistry
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