Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 서명은 | * |
dc.contributor.author | 유희원 | * |
dc.date.accessioned | 2018-12-27T16:30:06Z | - |
dc.date.available | 2018-12-27T16:30:06Z | - |
dc.date.issued | 1997 | * |
dc.identifier.issn | 0253-2964 | * |
dc.identifier.other | OAK-17038 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/247965 | - |
dc.description.abstract | The angular and planar heterocyclic compounds containing nitrogen, sulfur and oxygen were synthesized by reaction of 6,7-dichloro-5,8-quinoxalinedione with aromatic and aliphatic dinucleophiles. Nucleophilic reactivity was somewhat different between 2,3-dichloro-1,4-naphthoquinone and 6,7-dichloro-5,8-quinolinedione with dinucleophiles. The distribution of electron in heterocycle appeared to contribute to this difference. The intercalation comple of planar heterocyclic compound between GC/GC base pairs showed the optimum intercalation but the intercalation of angular heterocyclic compound was not good. Thus, the planar compound was expected to have antitumor activity. | * |
dc.language | English | * |
dc.title | The Reaction of 6,7-Dichloro-5,8-quinoxalinedione with Aromatic and Aliphatic Dinucleophiles and Molecular Modeling Study, of Their Intercalation Complexes | * |
dc.type | Article | * |
dc.relation.issue | 5 | * |
dc.relation.volume | 18 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.index | KCI | * |
dc.relation.startpage | 484 | * |
dc.relation.lastpage | 488 | * |
dc.relation.journaltitle | Bulletin of the Korean Chemical Society | * |
dc.identifier.scopusid | 2-s2.0-0031350425 | * |
dc.author.google | Yoo H.-W. | * |
dc.author.google | Suh M.-E. | * |
dc.author.google | Shin K.J. | * |
dc.author.google | Park S.-W. | * |
dc.contributor.scopusid | 서명은(7103253844) | * |
dc.date.modifydate | 20240423081003 | * |