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dc.contributor.author한소엽-
dc.date.accessioned2017-01-05T02:01:24Z-
dc.date.available2017-01-05T02:01:24Z-
dc.date.issued2003-
dc.identifier.issn0040-4039-
dc.identifier.otherOAK-1388-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/233743-
dc.description.abstractWe successfully synthesized a 14-membered cyclic enamide of C3-epimauritine D from the cis-2,3-pyrrolidinediol derivative. Treatment of the pyrrolidinediol with nitrobenzonitrile in an SNAr reaction efficiently installed the desired aryl-alkyl ether linkage on the N-heterocyclic system. Macrocyclization was successfully achieved by the use of TFFH as the peptide coupling reagent in the presence of HOAt. © 2003 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.titleStudies toward a synthesis of C3-epimauritine D: Construction of the macrocycle-
dc.typeArticle-
dc.relation.issue12-
dc.relation.volume44-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage2557-
dc.relation.lastpage2560-
dc.relation.journaltitleTetrahedron Letters-
dc.identifier.doi10.1016/S0040-4039(03)00278-8-
dc.identifier.wosidWOS:000181575200029-
dc.identifier.scopusid2-s2.0-0037450911-
dc.author.googleKim Y.-A.-
dc.author.googleShin H.-N.-
dc.author.googlePark M.-S.-
dc.author.googleCho S.-H.-
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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