完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Annamalai, Pratheepkumar | en_US |
dc.contributor.author | Hsu, Kou-Chi | en_US |
dc.contributor.author | Raju, Selvam | en_US |
dc.contributor.author | Hsiao, Huan-Chang | en_US |
dc.contributor.author | Chou, Chih-Wei | en_US |
dc.contributor.author | Lin, Gu-Ying | en_US |
dc.contributor.author | Hsieh, Cheng-Ming | en_US |
dc.contributor.author | Chen, Pei-Ling | en_US |
dc.contributor.author | Liu, Yi-Hung | en_US |
dc.contributor.author | Chuang, Shih-Ching | en_US |
dc.date.accessioned | 2018-08-21T05:53:32Z | - |
dc.date.available | 2018-08-21T05:53:32Z | - |
dc.date.issued | 2018-04-06 | en_US |
dc.identifier.issn | 0022-3263 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1021/acs.joc.8b00194 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/144834 | - |
dc.description.abstract | We developed palladium-catalyzed oxidative coupling of olefins with N-acyl 2-aminobiaryls through a sequence of ortho C-H bond activation/alkene insertion/reductive elimination. Furthermore, we controlled the selectivity of mono- and bis-alkenylation products with the solvent effect. The developed protocol was promising for a broad substrate scope ranging from activated olefins with a wide variety of functional groups to unactivated olefins. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Palladium(II)-Catalyzed Mono- and Bis-alkenylation of N-Acetyl-2-aminobiaryls through Regioselective C-H Bond Activation | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1021/acs.joc.8b00194 | en_US |
dc.identifier.journal | JOURNAL OF ORGANIC CHEMISTRY | en_US |
dc.citation.volume | 83 | en_US |
dc.citation.spage | 3840 | en_US |
dc.citation.epage | 3856 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000429886100041 | en_US |
顯示於類別: | 期刊論文 |