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dc.contributor.authorIm, DS-
dc.contributor.authorCheong, CS-
dc.contributor.authorLee, SH-
dc.contributor.authorYoun, BH-
dc.contributor.authorKim, SC-
dc.date.accessioned2024-01-21T14:12:01Z-
dc.date.available2024-01-21T14:12:01Z-
dc.date.created2021-09-05-
dc.date.issued2000-03-03-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141505-
dc.description.abstract(+/-)-2-Cyano-2-phenyl-1-hexanol 3 was resolved to each enantiomer using Candida rugosa and Pseudomonas fluorescens lipases in 62 and 99% ee, respectively. The absolute stereochemistry of one of the enantiomers was determined to be (S) by diastereomeric amide formation and X-ray crystallography. The resolved alcohols of (R)- and (S)-isomer were transformed to Systhane(R) analogues. (C) 2000 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectRESOLUTIONS-
dc.subjectENANTIOMERS-
dc.subjectCARBON-
dc.titleChemoenzymatic synthesis of optically active 2-phenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4020(00)00031-4-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON, v.56, no.10, pp.1309 - 1314-
dc.citation.titleTETRAHEDRON-
dc.citation.volume56-
dc.citation.number10-
dc.citation.startPage1309-
dc.citation.endPage1314-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000085669200004-
dc.identifier.scopusid2-s2.0-0007094304-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusRESOLUTIONS-
dc.subject.keywordPlusENANTIOMERS-
dc.subject.keywordPlusCARBON-
dc.subject.keywordAuthorchemoenzymatic-
dc.subject.keywordAuthorfungicide-
dc.subject.keywordAuthorquaternary carbon-
dc.subject.keywordAuthorlipase-catalyzed reaction-
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