Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 최선 | * |
dc.contributor.author | 류재상 | * |
dc.date.accessioned | 2016-08-28T11:08:05Z | - |
dc.date.available | 2016-08-28T11:08:05Z | - |
dc.date.issued | 2006 | * |
dc.identifier.issn | 0253-6269 | * |
dc.identifier.other | OAK-3356 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/219708 | - |
dc.description.abstract | An efficient method for the synthesis of optically active 2-substituted 2,3-dihydro-4-quinolones has been developed. The key features include the introduction of a chiral side chain and the construction of quinolone skeleton by Mitsunobu alkylation and hydroarylation, respectively. | * |
dc.language | English | * |
dc.title | Efficient synthesis of 2-substituted 2,3-dihydro-4-quinolones as potential intermediates for 2-substituted 1,2,3,4-tetrahydro-4-quinolone antitumor agents | * |
dc.type | Article | * |
dc.relation.issue | 5 | * |
dc.relation.volume | 29 | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.index | KCI | * |
dc.relation.startpage | 369 | * |
dc.relation.lastpage | 374 | * |
dc.relation.journaltitle | Archives of Pharmacal Research | * |
dc.identifier.wosid | WOS:000237932800005 | * |
dc.identifier.scopusid | 2-s2.0-33744924213 | * |
dc.author.google | Choi S. | * |
dc.author.google | Jung K. | * |
dc.author.google | Ryu J. | * |
dc.contributor.scopusid | 최선(8659831000) | * |
dc.contributor.scopusid | 류재상(36081118200) | * |
dc.date.modifydate | 20240305081003 | * |