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dc.contributor.author남상집*
dc.date.accessioned2016-08-29T12:08:17Z-
dc.date.available2016-08-29T12:08:17Z-
dc.date.issued2015*
dc.identifier.issn1523-7060*
dc.identifier.issn1523-7052*
dc.identifier.otherOAK-15236*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/230676-
dc.description.abstractChemical investigation of a marine actinomycete within the family Streptomycetaceae (our strain CNQ-149) has led to the isolation of the unprecedented alkaloids, actinobenzoquinoline (1) and actinophenanthrolines A-C (2-4). The chemical structures of 1-4 were assigned by interpretation of NMR spectroscopic data, and their absolute configurations were assigned by X-ray analysis. Actinobenzoquinoline possesses a 5-methyloxazolidin-4-one moiety and a dihydrobento[h],quinoline core structure, while actinophenanthrolines A-C are composed of hydroxypropanamide-substituted 1,7-phenanthroline core skeletons.*
dc.languageEnglish*
dc.publisherAMER CHEMICAL SOC*
dc.titleActinobenzoquinoline and Actinophenanthrolines A-C, Unprecedented Alkaloids from a Marine Actinobacterium*
dc.typeArticle*
dc.relation.issue13*
dc.relation.volume17*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage3240*
dc.relation.lastpage3243*
dc.relation.journaltitleORGANIC LETTERS*
dc.identifier.doi10.1021/acs.orglett.5b01387*
dc.identifier.wosidWOS:000357623900014*
dc.identifier.scopusid2-s2.0-84935083137*
dc.author.googleNam, Sang-Jip*
dc.author.googleKauffman, Christopher A.*
dc.author.googleJensen, Paul R.*
dc.author.googleMoore, Curtis E.*
dc.author.googleRheingold, Arnold L.*
dc.author.googleFenical, William*
dc.contributor.scopusid남상집(57208839798)*
dc.date.modifydate20240220120010*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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