DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, D | - |
dc.contributor.author | Choi, YK | - |
dc.contributor.author | Kim, MJ | - |
dc.date.accessioned | 2016-03-31T13:28:15Z | - |
dc.date.available | 2016-03-31T13:28:15Z | - |
dc.date.created | 2009-03-18 | - |
dc.date.issued | 2000-08-10 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.other | 2000-OAK-0000001488 | - |
dc.identifier.uri | https://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.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.relation.isPartOf | ORGANIC LETTERS | - |
dc.subject | ORGANIC-SOLVENTS | - |
dc.subject | ENANTIOMERICALLY PURE | - |
dc.subject | CHEMICAL MODIFICATION | - |
dc.subject | ALPHA-CHYMOTRYPSIN | - |
dc.subject | BUILDING-BLOCKS | - |
dc.subject | ALCOHOLS | - |
dc.subject | SELECTIVITY | - |
dc.subject | HYDROLYSIS | - |
dc.subject | RESOLUTION | - |
dc.subject | INCREASE | - |
dc.title | Enhancing the enantioselectivity of lipase in transesterification by substrate matching: An enzyme memory based approach | - |
dc.type | Article | - |
dc.contributor.college | 화학과 | - |
dc.identifier.doi | 10.1021/ol0062897 | - |
dc.author.google | Lee, D | - |
dc.author.google | Choi, YK | - |
dc.author.google | Kim, MJ | - |
dc.relation.volume | 2 | - |
dc.relation.issue | 16 | - |
dc.relation.startpage | 2553 | - |
dc.relation.lastpage | 2555 | - |
dc.contributor.id | 10052207 | - |
dc.relation.journal | ORGANIC LETTERS | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | ORGANIC LETTERS, v.2, no.16, pp.2553 - 2555 | - |
dc.identifier.wosid | 000088605200042 | - |
dc.date.tcdate | 2019-01-01 | - |
dc.citation.endPage | 2555 | - |
dc.citation.number | 16 | - |
dc.citation.startPage | 2553 | - |
dc.citation.title | ORGANIC LETTERS | - |
dc.citation.volume | 2 | - |
dc.contributor.affiliatedAuthor | Kim, MJ | - |
dc.identifier.scopusid | 2-s2.0-0034632430 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 26 | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | ORGANIC-SOLVENTS | - |
dc.subject.keywordPlus | ENANTIOMERICALLY PURE | - |
dc.subject.keywordPlus | CHEMICAL MODIFICATION | - |
dc.subject.keywordPlus | ALPHA-CHYMOTRYPSIN | - |
dc.subject.keywordPlus | BUILDING-BLOCKS | - |
dc.subject.keywordPlus | ALCOHOLS | - |
dc.subject.keywordPlus | SELECTIVITY | - |
dc.subject.keywordPlus | HYDROLYSIS | - |
dc.subject.keywordPlus | RESOLUTION | - |
dc.subject.keywordPlus | INCREASE | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
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