Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김원석 | * |
dc.date.accessioned | 2016-09-21T01:09:15Z | - |
dc.date.available | 2016-09-21T01:09:15Z | - |
dc.date.issued | 2016 | * |
dc.identifier.issn | 0022-3263 | * |
dc.identifier.other | OAK-19298 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/232244 | - |
dc.description.abstract | A new and mild synthetic approach for the N-arylation of 2-pyridones with diaryliodonium salts has been developed. Most reactions proceed readily at room temperature in the presence of 10 mol % of copper chloride. As a result, a wide range of N-arylpyridine-2-ones were synthesized in yields of 23% to 99%. With this method, an antifibrotic drug, Pirfenidone, was successfully synthesized in 99% yield within 30 min at room temperature. | * |
dc.language | English | * |
dc.publisher | AMER CHEMICAL SOC | * |
dc.title | Copper-Catalyzed N-Arylation of 2-Pyridones Employing Diaryliodonium Salts at Room Temperature | * |
dc.type | Article | * |
dc.relation.issue | 17 | * |
dc.relation.volume | 81 | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 7717 | * |
dc.relation.lastpage | 7724 | * |
dc.relation.journaltitle | JOURNAL OF ORGANIC CHEMISTRY | * |
dc.identifier.doi | 10.1021/acs.joc.6b01415 | * |
dc.identifier.wosid | WOS:000382713800042 | * |
dc.identifier.scopusid | 2-s2.0-84985019835 | * |
dc.author.google | Jung, Seo-Hee | * |
dc.author.google | Sung, Dan-Bi | * |
dc.author.google | Park, Cho-Hee | * |
dc.author.google | Kim, Won-Suk | * |
dc.contributor.scopusid | 김원석(57203484044) | * |
dc.date.modifydate | 20240220102223 | * |