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Cited 28 time in webofscience Cited 27 time in scopus
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dc.contributor.authorLee, D-
dc.contributor.authorChoi, YK-
dc.contributor.authorKim, MJ-
dc.date.accessioned2016-03-31T13:28:15Z-
dc.date.available2016-03-31T13:28:15Z-
dc.date.created2009-03-18-
dc.date.issued2000-08-10-
dc.identifier.issn1523-7060-
dc.identifier.other2000-OAK-0000001488-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19898-
dc.description.abstract[GRAPHICS] The substrate matching strategy is described as a new approach for effectively enhancing the lipase enantioselectivity in organic solvent. In the lipase-catalyzed transesterifications of 3a-c, higher enantioselectivities have been achieved using 1a-c, respectively, as the structurally matched acyl donors.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfORGANIC LETTERS-
dc.subjectORGANIC-SOLVENTS-
dc.subjectENANTIOMERICALLY PURE-
dc.subjectCHEMICAL MODIFICATION-
dc.subjectALPHA-CHYMOTRYPSIN-
dc.subjectBUILDING-BLOCKS-
dc.subjectALCOHOLS-
dc.subjectSELECTIVITY-
dc.subjectHYDROLYSIS-
dc.subjectRESOLUTION-
dc.subjectINCREASE-
dc.titleEnhancing the enantioselectivity of lipase in transesterification by substrate matching: An enzyme memory based approach-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1021/ol0062897-
dc.author.googleLee, D-
dc.author.googleChoi, YK-
dc.author.googleKim, MJ-
dc.relation.volume2-
dc.relation.issue16-
dc.relation.startpage2553-
dc.relation.lastpage2555-
dc.contributor.id10052207-
dc.relation.journalORGANIC LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.2, no.16, pp.2553 - 2555-
dc.identifier.wosid000088605200042-
dc.date.tcdate2019-01-01-
dc.citation.endPage2555-
dc.citation.number16-
dc.citation.startPage2553-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume2-
dc.contributor.affiliatedAuthorKim, MJ-
dc.identifier.scopusid2-s2.0-0034632430-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc26-
dc.type.docTypeArticle-
dc.subject.keywordPlusORGANIC-SOLVENTS-
dc.subject.keywordPlusENANTIOMERICALLY PURE-
dc.subject.keywordPlusCHEMICAL MODIFICATION-
dc.subject.keywordPlusALPHA-CHYMOTRYPSIN-
dc.subject.keywordPlusBUILDING-BLOCKS-
dc.subject.keywordPlusALCOHOLS-
dc.subject.keywordPlusSELECTIVITY-
dc.subject.keywordPlusHYDROLYSIS-
dc.subject.keywordPlusRESOLUTION-
dc.subject.keywordPlusINCREASE-
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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