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dc.contributor.author윤주영*
dc.date.accessioned2017-01-18T02:01:34Z-
dc.date.available2017-01-18T02:01:34Z-
dc.date.issued2007*
dc.identifier.issn0040-4039*
dc.identifier.otherOAK-4314*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/234007-
dc.description.abstractFacile methods are described for accessing four diastereomerically pure 3-mercaptoaspartic acid derivative from l-aspartic acid. In our synthesis, ring-opening reactions of oxazoline-4,5-dicarboxylate with thiolacetic acid as well as the stereochemical interconversion of both α- and β-configuration via oxazoline chemistry were utilized as key steps. © 2007 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleRing-opening of oxazolines derived from l-serine: a short and efficient stereoselective synthesis of all four diastereomers of 3-mercaptoaspartic acid derivatives*
dc.typeArticle*
dc.relation.issue41*
dc.relation.volume48*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage7309*
dc.relation.lastpage7312*
dc.relation.journaltitleTetrahedron Letters*
dc.identifier.doi10.1016/j.tetlet.2007.08.041*
dc.identifier.wosidWOS:000249846600013*
dc.identifier.scopusid2-s2.0-34548500781*
dc.author.googleLee S.-H.*
dc.author.googleBok J.*
dc.author.googleQi X.*
dc.author.googleKim S.K.*
dc.author.googleLee Y.-S.*
dc.author.googleYoon J.*
dc.contributor.scopusid윤주영(7403587371)*
dc.date.modifydate20240118162450*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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