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dc.contributor.authorPark, JN-
dc.contributor.authorKo, SY-
dc.contributor.authorKoh, HY-
dc.date.accessioned2024-01-21T13:41:38Z-
dc.date.available2024-01-21T13:41:38Z-
dc.date.created2021-09-05-
dc.date.issued2000-07-15-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141227-
dc.description.abstractChloramphenicol and 4-epi-cytoxazone have been enantioselectively synthesized using the asymmetric dihydroxylation and the cyclic iminocarbonate rearrangement as key steps. (C) 2000 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectBETA-AMINO ACIDS-
dc.subjectCYTOKINE MODULATOR-
dc.subjectASYMMETRIC AMINOHYDROXYLATION-
dc.subjectCYTOXAZONE-
dc.subjectDIHYDROXYLATION-
dc.titleSynthetic applications of the cyclic iminocarbonate rearrangement: enantioselective syntheses of chloramphenicol and 4-epi-cytoxazone-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(00)00878-9-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.41, no.29, pp.5553 - 5556-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume41-
dc.citation.number29-
dc.citation.startPage5553-
dc.citation.endPage5556-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000088200200025-
dc.identifier.scopusid2-s2.0-0000862806-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusBETA-AMINO ACIDS-
dc.subject.keywordPlusCYTOKINE MODULATOR-
dc.subject.keywordPlusASYMMETRIC AMINOHYDROXYLATION-
dc.subject.keywordPlusCYTOXAZONE-
dc.subject.keywordPlusDIHYDROXYLATION-
dc.subject.keywordAuthorenantioselective synthesis-
dc.subject.keywordAuthorcyclic iminocarbonate rearrangement-
dc.subject.keywordAuthorregioselection-
dc.subject.keywordAuthorchloramphenicol-
dc.subject.keywordAuthor4-epi-cytoxazone-
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