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dc.contributor.authorLiu, Zhiguo-
dc.contributor.authorYoon, Goo-
dc.contributor.authorCheon, Seung Hoon-
dc.date.accessioned2024-01-20T19:32:03Z-
dc.date.available2024-01-20T19:32:03Z-
dc.date.created2021-09-02-
dc.date.issued2010-04-24-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/131537-
dc.description.abstractThe absolute configuration of (-)-licochalcone E (1) was determined to be (S) via the first enantioselective total synthesis of the compound. The chirality in (S)-(-)-licochalcone E (1) was installed by asymmetric methylation of the Evans oxazolidinone derivatives. (C) 2010 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectCHALCONES-
dc.titleAn enantioselective total synthesis of (S)-(-)-licochalcone E: determination of the absolute configuration-
dc.typeArticle-
dc.identifier.doi10.1016/j.tet.2010.02.089-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON, v.66, no.17, pp.3165 - 3172-
dc.citation.titleTETRAHEDRON-
dc.citation.volume66-
dc.citation.number17-
dc.citation.startPage3165-
dc.citation.endPage3172-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000276804800006-
dc.identifier.scopusid2-s2.0-77949918093-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCHALCONES-
dc.subject.keywordAuthorEnantioselective synthesis-
dc.subject.keywordAuthorLicochalcone E-
dc.subject.keywordAuthorAsymmetric methylation-
dc.subject.keywordAuthorChiral oxazolidinone-
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