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dc.contributor.author윤주영*
dc.date.accessioned2017-01-05T02:01:17Z-
dc.date.available2017-01-05T02:01:17Z-
dc.date.issued2003*
dc.identifier.issn0040-4020*
dc.identifier.otherOAK-1614*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/233703-
dc.description.abstractPaclitaxel analogues with a thiol group in place of the hydroxyl group on the C-13 side-chain constitute an interesting avenue of research for the study of new taxoid compounds. A synthetic route for the preparation of 2′-deoxy-2′-epi-mercaptopaclitaxel with high ee has been developed. The key step is the regio-controlled ring-opening reaction of the trans-oxazoline derivative with thiolacetic acid, which allows the introduction of the sulfur-containing group onto the side-chain. © 2003 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleSynthesis of novel taxoid analogue containing sulfur group on C-13 side-chain: 2′-deoxy-2′-epi-mercaptopaclitaxel*
dc.typeArticle*
dc.relation.issue37*
dc.relation.volume59*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage7409*
dc.relation.lastpage7412*
dc.relation.journaltitleTetrahedron*
dc.identifier.doi10.1016/S0040-4020(03)01098-6*
dc.identifier.wosidWOS:000185310700019*
dc.identifier.scopusid2-s2.0-0042382887*
dc.author.googleQi X.*
dc.author.googleLee S.-H.*
dc.author.googleYoon J.*
dc.author.googleLee Y.-S.*
dc.contributor.scopusid윤주영(7403587371)*
dc.date.modifydate20240118162450*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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