An expedient synthesis of (+)-quinolactacin A2

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dc.contributor.authorS J Park-
dc.contributor.authorK N Cho-
dc.contributor.authorWon Gon Kim-
dc.contributor.authorK I Lee-
dc.date.accessioned2017-04-19T09:01:45Z-
dc.date.available2017-04-19T09:01:45Z-
dc.date.issued2004-
dc.identifier.issn00404039-
dc.identifier.uri10.1016/j.tetlet.2004.10.001ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/6690-
dc.description.abstractAn expedient synthesis of quinolactacin A2 from N-methylisatoic anhydride and N-Boc-(2S,3S)-isoleucine has been achieved. The key step involves the Friedl?nder-type annulation of isatoic anhydride and β-ketoester derived from isoleucine.-
dc.publisherElsevier-
dc.titleAn expedient synthesis of (+)-quinolactacin A2-
dc.title.alternativeAn expedient synthesis of (+)-quinolactacin A2-
dc.typeArticle-
dc.citation.titleTetrahedron Letters-
dc.citation.number48-
dc.citation.endPage8795-
dc.citation.startPage8793-
dc.citation.volume45-
dc.contributor.affiliatedAuthorWon Gon Kim-
dc.contributor.alternativeName박수진-
dc.contributor.alternativeName조광님-
dc.contributor.alternativeName김원곤-
dc.contributor.alternativeName이기인-
dc.identifier.bibliographicCitationTetrahedron Letters, vol. 45, no. 48, pp. 8793-8795-
dc.identifier.doi10.1016/j.tetlet.2004.10.001-
dc.subject.keywordβ-ketoester-
dc.subject.keyword(+)-Quinolactacin A2-
dc.subject.keywordFriedlander-type annulation-
dc.subject.keywordIsatoic anhydride-
dc.subject.localβ-ketoester-
dc.subject.local(+)-Quinolactacin A2-
dc.subject.localFriedlander-type annulation-
dc.subject.localIsatoic anhydride-
dc.description.journalClassY-
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Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
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