Enzymatic preparation of optically active 2-acetoxymethylglycidol, a new chiral building block in natural product synthesis

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dc.contributor.authorYoung Bae Seu-
dc.contributor.authorYung Hee Kho-
dc.date.accessioned2017-04-19T08:44:10Z-
dc.date.available2017-04-19T08:44:10Z-
dc.date.issued1992-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3201-
dc.description.abstractAsymmetric hydrolysis of geminally disubstituted achiral diacetate 2 with lipase PPL yielded optically active (R)-(-)-2-acetoxymethylglycidol 3 and its reduction gave compound 6, useful as the tert-alcohol chiral building block.-
dc.publisherElsevier-
dc.titleEnzymatic preparation of optically active 2-acetoxymethylglycidol, a new chiral building block in natural product synthesis-
dc.title.alternativeEnzymatic preparation of optically active 2-acetoxymethylglycidol, a new chiral building block in natural product synthesis-
dc.typeArticle-
dc.citation.titleTetrahedron Letters-
dc.citation.number46-
dc.citation.endPage7016-
dc.citation.startPage7015-
dc.citation.volume33-
dc.contributor.affiliatedAuthorYoung Bae Seu-
dc.contributor.affiliatedAuthorYung Hee Kho-
dc.contributor.alternativeName서영배-
dc.contributor.alternativeName고영희-
dc.identifier.bibliographicCitationTetrahedron Letters, vol. 33, no. 46, pp. 7015-7016-
dc.identifier.doi10.1016/S0040-4039(00)60920-6-
dc.description.journalClassY-
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