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dc.contributor.author한소엽-
dc.date.accessioned2018-05-02T08:15:27Z-
dc.date.available2018-05-02T08:15:27Z-
dc.date.issued2004-
dc.identifier.issn0039-7911-
dc.identifier.otherOAK-2345-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/242698-
dc.description.abstractChloptosin is an apoptosis-inducing dimeric cyclohexapeptide. Enantio-selective synthesis of L-6-chloropyrroloindoline, as the key chiral synthon of the cyclohexapeptide of chloptosin, was successfully achieved starting from 3-chloroaniline by utilizing Fischer indole/Schöllkopf protocol and oxidative cyclization of resulting L-6-chlorotryptophan.-
dc.languageEnglish-
dc.titleSynthesis of L-6-chloropyrroloindoline of chloptosin cyclohexapeptide-
dc.typeArticle-
dc.relation.issue16-
dc.relation.volume34-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage2931-
dc.relation.lastpage2943-
dc.relation.journaltitleSynthetic Communications-
dc.identifier.doi10.1081/SCC-200026636-
dc.identifier.wosidWOS:000223876100008-
dc.identifier.scopusid2-s2.0-4544310313-
dc.author.googleKim Y.-A.-
dc.author.googleHan S.-Y.-
dc.contributor.scopusid한소엽(7405944194)-
dc.date.modifydate20200928112844-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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