Preparation of enantiomerically pure (R)-2-Butyryloxymethylglycidol by Lipase-Catalyzed Asymmetric Hydrolysis

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dc.contributor.authorYoung Bae Seu-
dc.contributor.author임태경-
dc.contributor.authorChang Jin Kim-
dc.contributor.author강순청-
dc.date.accessioned2017-04-19T08:45:10Z-
dc.date.available2017-04-19T08:45:10Z-
dc.date.issued1995-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3666-
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.publisherElsevier-
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-
dc.citation.number12-
dc.citation.endPage3014-
dc.citation.startPage3009-
dc.citation.volume6-
dc.contributor.affiliatedAuthorYoung Bae Seu-
dc.contributor.affiliatedAuthorChang Jin Kim-
dc.contributor.alternativeName서영배-
dc.contributor.alternativeName임태경-
dc.contributor.alternativeName김창진-
dc.contributor.alternativeName강순청-
dc.identifier.bibliographicCitationTetrahedron, vol. 6, no. 12, pp. 3009-3014-
dc.identifier.doi10.1016/0957-4166(95)00397-5-
dc.description.journalClassY-
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