Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 배윤수 | * |
dc.date.accessioned | 2016-08-28T12:08:44Z | - |
dc.date.available | 2016-08-28T12:08:44Z | - |
dc.date.issued | 2011 | * |
dc.identifier.issn | 0039-7881 | * |
dc.identifier.other | OAK-7625 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/221661 | - |
dc.description.abstract | Peripheral cross-coupling of the enol form of the 5-pyrazolone scaffold with arylboronic acids promoted by [PdCldppf)] afforded the arylated products in good yields. In this coupling, the protection of the enolizable hydroxyl group of pyrazolone is a prerequisite for ensuring the Suzuki-Miyaura cross-coupling. A particular feature of this process is that it enables the synthesis of 5-hydroxy-3-biphenyl and -terphenylpyrazole derivatives with structural diversity. © Georg Thieme Verlag Stuttgart - New York. | * |
dc.language | English | * |
dc.title | Palladium-catalyzed peripheral arylation of 5-pyrazolones via enolizable bond protection | * |
dc.type | Article | * |
dc.relation.issue | 11 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 1783 | * |
dc.relation.lastpage | 1791 | * |
dc.relation.journaltitle | Synthesis | * |
dc.identifier.doi | 10.1055/s-0030-1260018 | * |
dc.identifier.wosid | WOS:000290787100017 | * |
dc.identifier.scopusid | 2-s2.0-79956366442 | * |
dc.author.google | Bin H.-R. | * |
dc.author.google | Bae Y.S. | * |
dc.author.google | Kim G. | * |
dc.author.google | Lee K.-I. | * |
dc.contributor.scopusid | 배윤수(15031067200) | * |
dc.date.modifydate | 20240415133331 | * |