Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 남상집 | * |
dc.date.accessioned | 2016-08-29T12:08:17Z | - |
dc.date.available | 2016-08-29T12:08:17Z | - |
dc.date.issued | 2015 | * |
dc.identifier.issn | 1523-7060 | * |
dc.identifier.issn | 1523-7052 | * |
dc.identifier.other | OAK-15236 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/230676 | - |
dc.description.abstract | Chemical 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.language | English | * |
dc.publisher | AMER CHEMICAL SOC | * |
dc.title | Actinobenzoquinoline and Actinophenanthrolines A-C, Unprecedented Alkaloids from a Marine Actinobacterium | * |
dc.type | Article | * |
dc.relation.issue | 13 | * |
dc.relation.volume | 17 | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 3240 | * |
dc.relation.lastpage | 3243 | * |
dc.relation.journaltitle | ORGANIC LETTERS | * |
dc.identifier.doi | 10.1021/acs.orglett.5b01387 | * |
dc.identifier.wosid | WOS:000357623900014 | * |
dc.identifier.scopusid | 2-s2.0-84935083137 | * |
dc.author.google | Nam, Sang-Jip | * |
dc.author.google | Kauffman, Christopher A. | * |
dc.author.google | Jensen, Paul R. | * |
dc.author.google | Moore, Curtis E. | * |
dc.author.google | Rheingold, Arnold L. | * |
dc.author.google | Fenical, William | * |
dc.contributor.scopusid | 남상집(57208839798) | * |
dc.date.modifydate | 20240220120010 | * |