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dc.contributor.authorAnnamalai, Pratheepkumaren_US
dc.contributor.authorHsu, Kou-Chien_US
dc.contributor.authorRaju, Selvamen_US
dc.contributor.authorHsiao, Huan-Changen_US
dc.contributor.authorChou, Chih-Weien_US
dc.contributor.authorLin, Gu-Yingen_US
dc.contributor.authorHsieh, Cheng-Mingen_US
dc.contributor.authorChen, Pei-Lingen_US
dc.contributor.authorLiu, Yi-Hungen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.date.accessioned2018-08-21T05:53:32Z-
dc.date.available2018-08-21T05:53:32Z-
dc.date.issued2018-04-06en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.joc.8b00194en_US
dc.identifier.urihttp://hdl.handle.net/11536/144834-
dc.description.abstractWe 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.isoen_USen_US
dc.titlePalladium(II)-Catalyzed Mono- and Bis-alkenylation of N-Acetyl-2-aminobiaryls through Regioselective C-H Bond Activationen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.joc.8b00194en_US
dc.identifier.journalJOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volume83en_US
dc.citation.spage3840en_US
dc.citation.epage3856en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000429886100041en_US
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