Preparation of Enantiomerically Pure (R)-2-Butyryloxymethylglycidol by Lipase-Catalyzed Asymmetric Hydrolysis

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dc.contributor.authorYoung Bae Seu-
dc.contributor.authorTaeg Kyeong Lim-
dc.contributor.authorChang Jin Kim-
dc.contributor.authorSun Chul Kang-
dc.date.accessioned2017-04-19T08:58:03Z-
dc.date.available2017-04-19T08:58:03Z-
dc.date.issued1995-
dc.identifier.issn0957-4166-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/5509-
dc.description.abstractOptically active epoxy alcohol, (R)-2-butyryloxymethylglycidol 3 which is the precursor of a tert-alcohol chiral building block was obtained in high enantiomeric purity, 98.7% e.e., by lipase-catalyzed asymmetric hydrolysis using a phosphate buffer and organic co-solvent system in 95% of chemical yield.-
dc.publisherElsevierko
dc.titlePreparation of Enantiomerically Pure (R)-2-Butyryloxymethylglycidol by Lipase-Catalyzed Asymmetric Hydrolysis-
dc.title.alternativePreparation of Enantiomerically Pure (R)-2-Butyryloxymethylglycidol by Lipase-Catalyzed Asymmetric Hydrolysis-
dc.typeArticle-
dc.citation.titleTetrahedron : Asymmetry-
dc.citation.number12-
dc.citation.endPage3014-
dc.citation.startPage3009-
dc.citation.volume6-
dc.contributor.affiliatedAuthorYoung Bae Seu-
dc.contributor.affiliatedAuthorTaeg Kyeong Lim-
dc.contributor.affiliatedAuthorChang Jin Kim-
dc.contributor.alternativeName서영배-
dc.contributor.alternativeName임택경-
dc.contributor.alternativeName김창진-
dc.contributor.alternativeName강선철-
dc.identifier.bibliographicCitationTetrahedron : Asymmetry, vol. 6, no. 12, pp. 3009-3014-
dc.identifier.doi10.1016/0957-4166(95)00397-5-
dc.description.journalClassN-
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